Inherited Porphyrias

CHAPTER

99

Inherited Porphyrias R J Desnick and Manisha Balwani Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine of New York University, New York, NY, USA

Karl E Anderson Departments of Preventive Medicine and Community Health (Division of Human Nutrition), Internal Medicine (Division of Gastroenterology) and Pharmacology and Toxicology, University of Texas Medical Branch/UTMB HealthGalveston, TX, USA

This article is a revision of the previous edition article by Robert J Desnick, Kenneth H Astrin and Karl E Anderson, volume 3, pp 2331–2358, © 2007, Elsevier Ltd.

99.1 INTRODUCTION The inherited porphyrias are a diverse group of inborn errors of metabolism, with each resulting from the deficient activity of a specific enzyme in the heme biosynthetic pathway (Tables 99-1 and 99-2). The resultant accumulation of porphyrin precursors and/or porphyrins causes the major clinical manifestations, neurologic symptoms, and/or cutaneous photosensitivity. These seven disorders are classified metabolically as hepatic or erythropoietic, depending on the primary source of their accumulated heme biosynthetic intermediates. They also are classified clinically as acute or cutaneous. Of the five hepatic porphyrias, four are characterized by life-threatening acute attacks of neurologic manifestations that occur in association with excess amounts of the porphyrin precursors, 5-aminolevulinic acid (ALA), and porphobilinogen (PBG), and they are classified as acute porphyrias. Three porphyrias have primarily cutaneous manifestations, including the two erythropoietic porphyrias and porphyria cutanea tarda (PCT). Two other hepatic porphyrias, hereditary coproporphyria (HCP) and variegate porphyria (VP), may cause acute neurologic attacks and cutaneous manifestations. The skin damage results from photoactivation of the accumulated porphyrins by longwave ultraviolet (UV) light. From a genetic point of view, the porphyrias are unique as five of the seven disorders are autosomal dominant enzymopathies. Of note, only a minority of heterozygotes becomes symptomatic. The onset and severity of the hepatic porphyrias are greatly influenced by environmental and metabolic factors, such as hormones, drugs, and nutrition. In addition, modifying genes presumably play an important role in the clinical expression of these disorders.

Here, we describe the clinical, metabolic, and genetic features of the seven porphyrias; mutations in the first enzyme in the heme biosynthetic pathway cause X-linked sideroblastic anemia (1). Optimal methods for their diagnosis and treatment are presented, and the current understanding of the genetic basis and disease pathogenesis in these acute and cutaneous disorders are discussed. Recent reviews on the inherited porphyrias are available (1–5). For lists of mutations causing each porphyria, please see the Human Gene Mutation Database (www.hgmd.org) (6). Informative and up-to-date Web sites are sponsored by the American Porphyria Foundation (www.porphyriafoundation.com) and the European Porphyria Initiative (www.porphyria-europe.org).

99.2 THE HEME BIOSYNTHETIC PATHWAY 99.2.1 The Heme Biosynthetic Enzymes The heme biosynthetic pathway is shown in Figure 99-1 and Table 99-1. Nine nuclear heme biosynthetic genes, including separate genes for the housekeeping and ­erythroid-specific isozymes of ALA-synthase, encode the enzymes that catalyze the eight steps in the conversion of glycine and succinyl-CoA to heme (1). The first and the last three enzymes are in the mitochondrion, and the other four function in the cytosol. The characteristics of the genes, their respective enzymes, and their chromosomal locations are summarized in Table 99-1. The heme biosynthetic pathway is responsible for the production of heme for hemoproteins, including the superfamily of cytochrome P450 enzymes, which are most abundant in the liver, and hemoglobin in erythrocytes.

© 2013, Elsevier Ltd. All rights reserved.

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CHAPTER 99  Inherited Porphyrias

TA B L E 9 9 - 1    Human Heme Biosynthesis Enzymes and Genesa Enzyme

Gene Symbol

Chromosomal Location

5-Aminolevulinate synthase: (ALA-synthase) Housekeeping ALAS1 3p21.1 Erythroid-specific ALAS2 Xp11.2 5-Aminolevulinate dehydratase: (ALA-dehydratase) Housekeeping ALAD 9q32 Erythroid-specific ALAD 9q32 Hydroxymethylbilane synthase: (HMB-synthase) Housekeeping HMBS 11q23.3 Erythroid-specific HMBS 11q23.3 Uroporphyrinogen III synthase: (URO-synthase) Housekeeping UROS 10q26.2 Erythroid-specific UROS 10q26.2 Uroporphyrinogen UROD 1p34.1 decarboxylase Coproporphyrinogen CPO 3q12.1 oxidase Protoporphyrinogen PPOX 1q23.3 oxidase Ferrochelatase FECH 18q21.31

Gene cDNA (bp)

Protein (aa)

Size (kb)

Exonsb

2,199 1,937

640 587

17 22

11 11

1,149 1,154

330 330

15.9 15.9

12 (1A + 2–12) 12 (1B + 2–12)

1,086 1,035

361 344

11 11

15 (1 + 3–15) 15 (2–15)

1,296 1,216 1,104

265 265 367

34 34 3

1,062

354

14

10 (1 + 2B-10) (2A + 2B-10) 10(URO-­ decarboxylase) 7(COPRO-oxidase)

1,431

477

5.5

13(PROTO-oxidase)

1,269

423

45

11

aReferences

in Anderson KE, Sassa S, Bishop DF, et al. (2001) Disorders of heme biosynthesis: X-linked sideroblastic anemias and the porphyrias. In Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The Metabolic and Molecular Basis of Inherited Disease, 8th ed. McGraw-Hill, New York, p 2991. bNumber of exons and (in parentheses) those encoding separate housekeeping and erythroid-specific forms.

Different regulatory controls have evolved for hepatic and erythroid-specific heme synthesis, including negative feedback repression by heme in the liver, and separate erythroid-specific genes or promoters in the first four genes in the pathway (Figure 99-2). Each of the enzymatic steps in the pathway is briefly described in this chapter. 99.2.1.1 5-Aminolevulinate Synthase.  The first enzyme in the pathway, 5-aminolevulinate synthase (ALA-synthase; also known as d-aminolevulinate synthase; E.C. 2.3.1.37), catalyzes the condensation of glycine (activated by pyridoxal phosphate) and succinyl coenzyme A to form ALA. Distinct human housekeeping and erythroid-specific ALA-synthase isozymes are encoded by separate genes: the ~17-kb housekeeping gene (ALAS1), located at chromosome 3p21.1, is expressed in all tissues, while the ~22-kb ­erythroid-specific gene (ALAS2), located at chromosome Xp11.21, is expressed only in erythroid cells to supply the large amounts of heme required for hemoglobin (see Figure 99-2). These findings provide a basis for the tissue-specific regulation of this pathway (for a review see Reference (1)). Of note, expression of the housekeeping gene ALAS1 in the liver is under ­negative feedback repression by the cellular heme ­concentration and functions to modulate the supply of heme for the hepatic cytochrome P450 enzymes and other hepatic hemoproteins (7). In acute porphyrias, the depletion of hepatic heme by various drugs, hormones, and glucose restriction, the increased synthesis of the housekeeping ALAS1 isozyme, and the generation of

the large amount of the porphyrin precursors, ALA and PBG, are the biochemical hallmarks of acute neurologic attacks (2). Mutations in the X-linked ALAS2 gene and the resultant deficient activity of the erythroid-specific isozyme cause X-linked sideroblastic anemia (1,8). Over 35 mutations in the erythroid-specific ALA-synthase gene causing X-linked sideroblastic anemia are listed in the Human Gene Mutation Database (www.hgmd.org) (6). Except for a mutation in the promoter region of the ALAS2 gene (9) and one nonsense mutation, all of the reported lesions have been missense mutations in the ALAS2 catalytic core encoded by exons 5 to 11, with the majority occurring in exons 5 and 9. Most mutations were pyridoxine responsive in vivo and when expressed in Escherichia coli. Molecular modeling of the ALAS2 isozyme, based on the crystal structure of a bacterial ALA-synthase, suggested the molecular basis for the pyridoxine responsiveness of certain mutations (10). Recently, gain of function mutations in exon 11 of ALAS2 that increase its activity have been shown to cause an X-linked form of erythropoetic protoporphyria (EPP), known as X-linked protoporphyria (XLP). To date, only two gain of function mutations in ALAS2 have been described. No deficiencies of the ALAS1 isozyme have been described; presumably, the enzymatic deficiency would be lethal. 99.2.1.2 5-Aminolevulinic Acid Dehydratase.  The second enzyme in the pathway is 5-aminolevulinic acid dehydratase (ALA-dehydratase; also known as PBG synthase; E.C. 4.2.1.24). This enzyme catalyzes the

TAB L E 9 9 - 2     Classification of the Human Porphyrias including Major Clinical and Biochemical Features Biochemical Findingsa

5-ALA ­dehydratase-porphyria (ADP) Acute intermittent (AIP) Congenital erythropoietic porphyria (CEP) Porphyria cutanea tarda (PCT)

Erythropoietic ­protoporphyria (EPP)

Enzyme Hb

H or E AR

Principal Inheritance NV

HMB-synthase URO-synthase

H E

AD AR

NV CP

URO-decarboxylase

H

ADc

URO- decarboxylase

H

COPRO-oxidase

Deficient NV or CP Zn-Protoporphyrin

Classification Erythrocytes ALA, Coproporphyrin III

Urine Stool — deficient

AR

CP

Zn-Protoporphyrin

H

AD

—

PROTO-oxidase

H

AD

NV & CP ­(uncommon) NV & CP

ALA, PBG, Uroporphyrin Uroporphyrin I ­ Coproporphyrin I Uroporphyrin, 7-carboxylate porphyrin Uroporphyrin, 7-carboxylate porphyrin ALA, PBG, Coproporphyrin III

— porphyria Coproporphyrin I

CP

— Uroporphyrin I ­Coproporphyrin I —

—

ALA, PBG, Coproporphyrin III

Ferrochelatase

E

ADd

CP

Protoporphyrin

—

Isocoproporphyrin Isocoproporphyrin Coproporphyrin III Coproporphyrin III Protoporphyrin Protoporphyrin

H, hepatic; E, erythropoietic; AR, autosomal recessive; AD, autosomal dominant; Type I isomers: ALA = 5-aminolevulinic acid; PBG = porphyrinogen; NV, neurovisceral; CP, cutaneous photosensitivity. aIncreases that may be important for diagnosis. bThese porphyrias also have erythropoietic features including increased erythrocyte porphyrins. cInherited deficiency of UROD is partially responsible for familial (Type II) PCT. dPolymorphism in intron 3 of wild-type allele affects level of enzyme activity and clinical expression.

CHAPTER 99  Inherited Porphyrias

Hepatoerythropoietic porphyria (HEP) Hereditary coproporphyria (HCP) Variegate porphyria (VP)

Symptomatology Porphyria 5-ALA-dehydratase

3

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CHAPTER 99  Inherited Porphyrias

FIGURE 99-1  The human heme biosynthetic pathway. Ac, acetyl; Pr, proponyl. condensation of two molecules of ALA to form the cyclic pyrrole, PBG (see Figure 99-1). Human ALA-dehydratase is composed of eight identical 31-kDa subunits and eight atoms of zinc, which are required for both enzyme stability and catalytic activity. The zinc atoms are bound to each subunit by a typical zinc finger domain consisting of four cysteine and two histidine residues (1). The zinc atoms protect essential sulfhydryl groups in the enzyme and can be displaced by lead or other heavy metals. In fact, the measurement of erythrocyte ALA-dehydratase activity is a highly sensitive index of lead exposure. The 16-kb human ALA-dehydratase gene encodes housekeeping and erythroid-specific transcripts by alternative splicing (11); see Figure 99-2. Both transcripts encode the same amino acid sequence, as translation begins in exon 2. The housekeeping promoter region is upstream of exon 1A, while the erythroid-specific promoter is upstream of exon 1B. Mutations in the ALA-dehydratase gene result in the deficiency of ALAdehydratase, causing a rare, recessively inherited acute hepatic porphyria, ALA- dehydratase-deficient porphyria (ADP) (6,12,13). Only six cases of ADP with 13 different ALA-dehydratase mutations have been reported (www. hgmd.org) (6,14). Of note, there are two common alleles at the ALAdehydratase locus, ALAD1 and ALAD2, which are responsible for three electrophoretically distinguishable enzyme forms designated 1–1, 1–2, and 2–2. The frequencies of the corresponding phenotypes in white populations are about 80%, 18%, and 1%, respectively,

giving gene frequencies of 0.9 and 0.1 for the ALAD1 and ALAD2 alleles, respectively. Gene frequency of the ALAD2 allele is lower in Hispanics, Asians, and ­African-Americans (15), and in a Liberian population, the ALAD2 allele was not detected. The ALAD2 allele has normal ALA-dehydratase activity but may bind zinc more effectively. Several epidemiologic studies have demonstrated an association between the ALAD2 allele and high lead levels (16–20). Although blood and serum lead levels were 5%–10% greater in individuals with the ALAD2 allele than in individuals with the other alleles, bone lead was not increased (17). 99.2.1.3 Hydroxymethylbilane Synthase.  Hydroxymethylbilane synthase (HMB-synthase; formerly known as PBG-deaminase or uroporphyrinogen I synthase; E.C. 4.3.1.8), the third enzyme in the pathway, catalyzes the head-to-tail condensation of four molecules of PBG by a series of deaminations to form the linear tetrapyrrole, hydroxymethylbilane (HMB) (see Figure 99-1). HMB can cyclize nonenzymatically to form uroporphyrinogen I, a nonphysiological and phototoxic compound. Because HMB-synthase activity is almost as low as ALA-synthase activity in the liver, it may become rate-limiting when the enzyme is partially deficient. The ~10-kb human HMB-synthase gene encodes erythroid-specific and housekeeping isozymes by alternative splicing (see Figure 99-2). The housekeeping and erythroid isozymes are monomeric proteins of 361 and 344 amino acid residues, respectively. The housekeeping promoter functions in all cell types, whereas the

CHAPTER 99  Inherited Porphyrias

Mitochondria

5

Cytoplasm

SUCCINYL COA COO CH CH2 CoAS C O

ALA Synthase B6 CoASH

H

CO2

H C NH2

COO

COO CH2 CH2 C=O H C NH H

Vi

HMBSynthase

Pr

Pr

Vi

Ac HO

CH3

Pr

Pr

N

CH3

N

Pr

Ac

CH

Pr

CH3

N

N

N

Pr

N N

CH

Ac

Pr

4CO2 Pr

Vi

Pr

4H

CH HH HH

N

H H H H

URO Decarboxylase

PROTO - Oxidase

N

N

UROPORPHYRINOGEN III

6H

Vi

Ac

Pr

PROTOPORPHYRIN IX

CH3

Ac

Pr

H2O

Ac

Vi

N H

N N

Pr

CH3 H

Pr

N

H H H H

UROSynthase

Ferrochelatase

Fe++

N

N

HYDROXYMETHYLBILANE

2H+

CH3

H

Ac

Ac

HEME

Vi

N H

4 NH3

CH3

N N Fe N N

CH3

NH2 CH2

CH2

PORPHOBILINOGEN

Feedback Repression CH3

CH2

CH2

H2O

5-AMINOLEVULINIC ACID

GLYCINE COO

COO

5-ALA Dehydratase

COPRO - Oxidase

CH3

2CO2 2H

CH3

Pr

N

N

H H H H

N N Pr

PROTOPORPHYRINOGEN IX

CH3 Pr CH3

Pr

COPROPORPHYRINOGEN III

FIGURE 99-2  The first four genes in the human heme biosynthetic pathway have housekeeping (PH) and erythroid-specific (PE) promoters and transcripts. The dotted lines indicate the exons transcribed by each promoter.

erythroid promoter functions only in erythroid cells. Human HMB-synthase has been purified from erythrocytes and its properties are characterized. Of note, the enzyme forms stable covalent enzyme–substrate complexes with PBG (21), and a unique dipyrromethane cofactor binds the di- and tri-pyrrole intermediates at the active site until the formation of HMB is complete (22).

Mutations in the HMB-synthase gene result in the deficient activity of HMB-synthase, causing acute intermittent porphyria (AIP), an autosomal dominant acute hepatic porphyria (23). Over 300 HMB-synthase ­mutations are listed in the Human Gene Mutation Database (www.hgmd.org) (6). Studies on crystallized ­HMB-synthase from E. coli showed that the protein is folded into three domains, each comprising b-strands and

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CHAPTER 99  Inherited Porphyrias

a-helices and a discrete hydrophobic core. Because the human and E. coli HMB-synthase amino acid sequences have about 35% homology and greater than 70% similarity, it was possible to infer the structure–function relationships for certain human HMB-synthase mutations from the bacterial enzyme (24,25). 99.2.1.4 Uroporphyrinogen III Synthase.  Uroporphyrinogen III synthase (URO-synthase; E.C. 4.2.1.75) catalyzes the rearrangement of HMB by inversion of the pyrrole D ring and ring closure to form the asymmetric uroporphyrinogen type III isomer (see Figure 99-1). In the absence of URO-synthase, HMB nonenzymatically cyclizes to form the uroporphyrinogen I isomer. This nonphysiologic compound can be metabolized to coproporphyrinogen I, but further metabolism cannot proceed as the next enzyme, coproporphyrinogen oxidase, is stereospecific for the III isomer. The ~34-kb human URO-synthase gene has alternative promoters that generate housekeeping and ­erythroid-specific transcripts, which encode the same 265 amino acid polypeptide (see Figure 99-2) (26). The enzyme is active as a 29.5-kDa monomer. The human enzyme has been crystallized at a resolution of 1.85 Å (27). The protein folds into two alpha/beta domains connected by a beta-ladder, with the active site between the domains. Mutations in the URO-synthase gene results in deficient but not absent, URO-synthase enzyme activity, causing congenital erythropoietic porphyria (CEP), an autosomal recessive erythropoietic porphyria (6,28). Over 35 URO-synthase mutations are listed in the Human Gene Mutation Database (www.hgmd.org) (6). 99.2.1.5 Uroporphyrinogen Decarboxylase.  Uroporphyrinogen-decarboxylase (E.C. 4.1.1.37), the fifth enzyme in the pathway, catalyzes the sequential removal of the four carboxyl groups from the acetic-acid side chains of uroporphyrinogen III (clockwise, starting with ring D) to form the four methyl groups of coproporphyrinogen III, a tetracarboxyl porphyrinogen (see Figure 99-1). The enzyme has no coenzyme or metal requirements, and iron does not appear to directly affect UROdecarboxylase activity in vitro. The ~3-kb human URO-decarboxylase gene has a ­single-mRNA species, which expresses a 367-residue polypeptide in all tissues, where it is active as a homodimer (29,30). Recombinant human URO-decarboxylase has been crystallized at 1.60-Å resolution, and its reaction mechanism has been studied (30–33). This enzyme is deficient in the liver in PCT, the most common porphyria. The majority (~80%) of PCT patients have no URO-decarboxylase mutations and are termed type I if the disease is sporadic or type III, if (rarely) more than one family member is affected. Heterozygous mutations and half-normal enzyme activities are found in all tissues (e.g. erythrocytes) in familial (type II) PCT (~20% of all PCT patients). In overt PCT of all types, hepatic URO-decarboxylase activity is always

reduced by additional factors to well below 50% of normal, which is consistent with an acquired tissue-specific inhibition of hepatic URO-decarboxylase. Hepatoerythropoietic porphyria (HEP) is the homozygous form of familial (type II) PCT and, generally, has a more severe phenotype (1,34). Over 100 URO-decarboxylase mutations identified in PCT and HEP are listed in the Human Gene Mutation Database (www.hgmd.org) (6). 99.2.1.6 Coproporphyrinogen Oxidase.  The sixth enzyme in the pathway, coproporphyrinogen oxidase (COPRO-oxidase; E.C. 1.3.3.3), catalyzes the decarboxylation of two of the four propionic acid groups of coproporphyrinogen III (on rings A and B) to form the two vinyl groups of protoporphyrinogen IX, a dicarboxyl porphyrinogen (see Figure 99-1). COPRO-oxidase is located between the mitochondrial inner and outer membranes, requires molecular oxygen for its activity, and contains no metals (1,35). An intermediate in the two-step decarboxylation is a 3-carboxyl porphyrinogen (termed harderoporphyrinogen, because this porphyrin in its oxidized form (harderoporphyrin) was first isolated from the rodent harderian gland). Coproporphyrinogen I, which is formed by decarboxylation of uroporphyrinogen I, is not a substrate for this enzyme and therefore is not metabolized to heme. The ~14-kb human COPRO-oxidase gene encodes a single transcript, which expresses a 474-residue polypeptide including an N-terminal mitochondrial, ­targeting signal peptide of 120 residues (36–38). Human ­COPRO-oxidase has been crystallized to a resolution of 1.58 Å (39). Studies of the crystal structure confirmed that COPRO-oxidase functions as a dimer and identified the residues in the enzyme’s active site (39). Mutations in the COPRO-oxidase gene result in deficient enzymatic activity, causing HCP, an autosomal dominant disorder (40). Over 40 COPRO-oxidase mutations are listed in the Human Gene Mutation Database (www.hgmd.org) (6). Mutation K404E in the COPROoxidase gene, when present in either the homozygous or compound heterozygous states, causes a biochemical variant, termed harderoporphyria (39,41). Cases of homozygous dominant HCP have also been described (6,42,43). 99.2.1.7 Protoporphyrinogen Oxidase.  The seventh enzyme in the pathway, protoporphyrinogen oxidase (PROTO-oxidase; E.C. 1.3.3.4), catalyzes the oxidation of protoporphyrinogen IX to protoporphyrin IX by the removal of six hydrogen atoms (see Figure 99-1). The product of the reaction is a porphyrin (oxidized form), in contrast to the preceding several products, which are porphyrinogens (reduced forms). This oxidation occurs readily in vitro under aerobic conditions in the absence of the enzyme. PROTO-oxidase is an integral protein of the mitochondrial inner membrane spacing and appears to be active as a dimer. PROTO-oxidase is inhibited by bilirubin, perhaps accounting for the decreased levels of the enzyme activity in Gilbert disease.

CHAPTER 99  Inherited Porphyrias The ~5.5-kb human PROTO-oxidase gene encodes a single ~1.8-kb mRNA in all tissues, which expresses a mitochondrial-targeted polypeptide of 477 amino acids (~51 kDa) (44–46). PROTO-oxidase lacks a typical mitochondrial targeting leader sequence but is effectively targeted by its 17 N-terminal residues (36). Mutations in the PROTO-oxidase gene result in 50% of normal enzymatic activity, causing VP, a dominantly inherited hepatic porphyria (47). Over 150 ­PROTO-oxidase mutations are listed in the Human Gene Mutation Database (www.hgmd.org) (6). Several cases of homozygous VP have also been described (48,49). 99.2.1.8 Ferrochelatase.  The final step in heme biosynthesis is the insertion of ferrous iron into protoporphyrin IX to form heme. This reaction is catalyzed by ferrochelatase (heme synthetase or protoheme ferrolyase; E.C. 4.99.1.1), which is associated with the inner side of the inner mitochondrial membrane. The enzyme is specific for the reduced form of iron (Fe2+) but can use other metals (e.g. Zn2+ and Co2+) and other 2-carboxyl porphyrins. The enzyme appears to function as a dimer in mitochondria (50), and there is suggestive evidence that the membrane domains of PROTO-oxidase dock onto the dimeric structure of ferrochelatase (51). The ~45-kb human ferrochelatase gene encodes a 423-amino acid polypeptide including a 54-residue leader sequence (36). An iron–sulfur cluster [2Fe-2S] has been identified in recombinant human and mouse ferrochelatase (52,53) and is thought to be essential for enzyme activity (54). The putative iron–sulfur binding site is at the C-terminus in a 30-amino acid region that contains four cysteines. Recombinant human ferrochelatase has been crystallized and diffracted to about 2 Å (55,56). Coding region mutations in the ferrochelatase gene result in a decreased enzymatic activity, causing erythropoietic protoporphyria (EPP) (57). Over 100 ferrochelatase mutations are listed in the Human Gene Mutation Database (www.hgmd.org) (6). Clinical expression of this porphyria occurs when a disabling ferrochelatase mutation is heteroallelic with a polymorphism in intron 3 of the wild-type ferrochelatase gene that reduces expression of normal enzyme (58) or, less commonly, in individuals who inherit two mutations that impair enzyme function (e.g. coding region or splice-site mutations).

99.3 REGULATION OF HEME BIOSYNTHESIS In humans, about 85% of heme is synthesized in erythroid cells to provide heme for hemoglobin, while most of the remaining heme is produced in the liver, where it is used primarily as the prosthetic group in cytochrome P450 enzymes and other hemoproteins. In the liver, the heme biosynthetic pathway is under a negative feedback control at the level of the first enzyme in the pathway, ALAS1 (the housekeeping form), by the concentration

7

of “free” heme (7). Heme represses the transcription and translation of liver ALAS1 mRNA, reduces ALAS1 mRNA stability (7), and interferes with the transport of the enzyme into mitochondria. High concentrations of free heme can also induce heme oxygenase and therefore stimulate heme catabolism (59). ALAS1 is inducible by many of the same chemicals that induce the hepatic cytochrome P450 enzymes. Because most of the heme synthesized in the liver is used for the synthesis of the cytochrome P450 enzymes, the induction of hepatic ­ALA-synthase and the cytochrome P450s occurs in a coordinated fashion. Recently, two sequence elements in the distal 5¢-flanking region of the human ALAS1 gene were identified, which mediate direct transcriptional activation in response to drugs metabolized by the cytochrome P450s (60). When the regulatory “free” heme pool becomes depleted (which may occur, for example, when more heme is required for the synthesis of hemoproteins), the synthesis of ALAS1 is increased. Conversely, repression of ALAS1 synthesis results from augmentation of the regulatory heme pool. The ­evidence that ALA-synthase1 functions as a rate-controlling enzyme, at least in the liver, includes its relatively low Vmax value (compared with most other enzymes in the pathway), its inducibility and short half-life, and its great sensitivity to repression by cellular heme (at concentrations below 10−6M). In addition, ALAS1 mRNA is markedly increased under conditions when more heme is required by cells while expression of the other enzymes in the pathway do not change significantly (7). The low affinity of the enzyme for glycine suggests that the intracellular glycine concentration also determines the rate of ALA formation. In erythroid cells, there are novel regulatory mechanisms for the production of the very large amounts of heme needed for hemoglobin synthesis. As noted ­previously, there is a separate erythroid-specific ALAsynthase gene (ALAS2) (1) and unique erythroid-specific promoters in ALA-dehydratase (11), HMB-synthase (23), and URO-synthase (61), the first four enzymes in the heme biosynthetic pathway (see Figure 99-2). The erythroid-specific gene ALAS2 on the X chromosome is expressed at high levels during erythroid differentiation. Synthesis of ALAS2, unlike ALAS1, is not repressed by hemin treatment and therefore is not regulated by the heme feedback repression. Transcriptional control of ALAS2 is exerted by erythroid-specific promoter elements in the 5¢-flanking region of the gene. Translational control results from an iron-responsive element in the 5¢-untranslated region of the mRNA. Transcription of the housekeeping ALAS1 gene may be downregulated during erythroid differentiation. In addition, heme regulates the rate of its synthesis in erythroid cells by controlling the transport of iron (required for ferrochelatase) into reticulocytes. Thus, the rate of iron acquisition from transferrin may be an important regulator of the erythroid heme biosynthesis (62).

8

CHAPTER 99  Inherited Porphyrias

These enzymes function in all cells to make heme for cytochromes and other hemoproteins. However, regulation of the heme biosynthesis in many tissues has not been the subject of intensive investigation, and some studies suggest that it may be different in tissues other than the liver and bone marrow (1).

99.4 CLASSIFICATION AND DIAGNOSIS OF THE PORPHYRIAS As mentioned previously, the porphyrias can be classified as either hepatic or erythropoietic, depending on whether the heme biosynthetic intermediates that accumulate arise initially from the liver or developing erythrocytes, or as acute or cutaneous, based on their clinical manifestations. Table 99-2 lists the porphyrias, their symptoms, major biochemical abnormalities, and inheritance patterns. Further details on the deficient enzymes are given in Table 99-3. Of the five hepatic porphyrias, four of them, acute intermittent porphyria (AIP), HCP, VP, and ALA-dehydratase porphyria (ADP), are present with acute attacks of neurologic manifestations and elevated levels of one or both of the porphyrin precursors, ALA and PBG, and are thus classified as acute porphyrias. Symptoms of neuropathic abdominal pain, peripheral neuropathy, and mental disturbances develop during adult life and are more common in women than in men (1,2,4). By contrast, PCT, while classified as a hepatic porphyria, presents with blistering skin lesions and not acute attacks. HCP and VP may cause cutaneous manifestations similar to PCT, in addition to acute neurological symptoms. The erythropoietic porphyrias, CEP, and EPP, are characterized by elevations of porphyrins in bone marrow and erythrocytes and present with

cutaneous photosensitivity. X-linked protoporphyria, a variant form of EPP, has a clinical presentation identical to classic EPP. Lesions in CEP resemble PCT but are usually much more severe, whereas EPP causes a more immediate, painful, and nonblistering type of photosensitivity. Homozygous dominant forms of AIP, HCP, VP, and familial (type II) PCT (known as HEP) and the autosomal recessive ADP also have erythropoietic features (e.g. increased erythrocyte porphyrins). Rare patients who have mutations in two different heme biosynthetic genes have also been described (see “Dual Porphyrias” section).

99.4.1 Diagnosis When porphyria is suspected clinically, proper laboratory testing is important to confirm or exclude the diagnosis for appropriate medical management and genetic counseling (2). Accuracy and speed are especially important in the diagnosis of an acute porphyric attack, so treatment can begin to prevent neurologic damage and even death. Tests for porphyria may be difficult to interpret because some abnormal results are seen in disorders other than the porphyrias; in particular, minimally elevated levels of urinary porphyrins may have little or no diagnostic significance. Table 99-3 summarizes the major metabolites that accumulate in each porphyria. However, for initial diagnosis of porphyrias, it is unwise to measure all of these intermediates routinely or attempt to identify a diagnostic profile. For initial screening, we recommend relying on a limited number of tests that are sensitive, specific, and cost effective; additional testing should be done only if a screening test is positive. Testing for elevated urinary

TA B L E 9 9 - 3    Human Porphyrias Associated with Deficiencies of Specific Enzymes of the Heme Biosynthetic Pathway Inheritance

Deficient Enzyme

Subcellular Localization

Enzyme Activity % of Normal

Known Mutations nd

Porphyria OMIM Numbera

5-ALA dehydratase-deficient Acute intermittent

125270 176000

AR AD

ALA-dehydratase HMB-synthase

C C

Congenital erythropoietic

263700

AR

URO-synthase

C

Porphyria cutanea tarda Hepatoerythropoietic

176100 176100

AD AR

URO-decarboxylase URO-decarboxylase

C C

Hereditary coproporphyria Variegate porphyria (VP) Erythropoietic

121300 176200 177000

AD AD ADc

COPRO-oxidase PROTO-oxidase Ferrochelatase

M M M

~5 9 porphyria (ADP) ~50244 porphyria (AIP) 1–5 36 porphyria (CEP) ~50b 55 (PCT, type II) 1–5 10 porphyria (HEP) ~50 37 (HCP) ~50 129 ~20–3088 protoporphyria (EPP)

AR, autosomal recessive; AD, autosomal dominant; C, cytosolic; M, mitochondrial. aOMIM, Online Mendelian Inheritance in Man (www.ncbi.nlm.nih.gov/entrez/query.fcgi?=OMIM). bClinical expression occurs when an iron-mediated inhibitor of URO-decarboxylase is generated and enzyme activity is further reduced (see text for details). cPolymorphism in intron 3 of wild-type allele affects level of enzyme activity and clinical expression. dNumber of known mutations from Human Gene Mutation Database (www.hgmd.org) as of March 29, 2006.

CHAPTER 99  Inherited Porphyrias PBG is especially important in screening for acute porphyrias. Active cutaneous porphyrias are readily detected by measuring total plasma porphyrin levels, although, if EPP is suspected, measurement of erythrocyte protoporphyrin is more sensitive. If a screening test result is abnormal, additional measurements are essential for establishing the specific type of porphyria (2). Urinary ALA and PBG are easily quantified by chemical methods (63), and the individual porphyrins in urine and feces can be separated and quantified by high-performance liquid chromatography. Assays are described in the literature for each of the eight heme biosynthetic enzymes, using erythrocytes, lymphocytes, cultured lymphoblasts, or cultured fibroblasts, although most are not widely available for diagnostic purposes (63). However, erythrocyte HMB-synthase activity is commonly measured to confirm the diagnosis of AIP and detect asymptomatic gene carriers. Establishing the definitive diagnosis of a particular porphyria should include identification of the causative gene mutation(s). This is the preferred method for detecting asymptomatic relatives who carry the mutation identified in an index case (2).

99.4.2 5-Aminolevulinic Acid Dehydratase-Deficient Porphyria (ADP) ALA-dehydratase-deficient porphyria (ADP) is a rare autosomal recessive acute hepatic porphyria caused by the severe deficiency of ALA-dehydratase activity (1,2). To date, only six cases have been reported with documentation by molecular methods (1,12–14). These affected homozygotes had less than 10% of normal ALA-dehydratase activity in erythrocytes, but their clinically asymptomatic parents and other heterozygous relatives had about half-normal levels of activity and did not excrete increased levels of ALA. The frequency of ADP is unknown, but the frequency of heterozygous individuals with less than 50% of normal ALA-dehydratase activity was ~2% in a screening study, in Sweden. Because there are multiple causes for deficient ALA-dehydratase activity, it is important to confirm the diagnosis of ADP by mutation analysis. 99.4.2.1 Biochemical Aspects.  ALA-dehydratasedeficient porphyria is characterized by the markedly increased urinary excretion of ALA and coproporphyrin III and increased erythrocyte protoporphyrin (complexed with zinc). The markedly reduced erythrocyte ALA-dehydratase activity in these patients is not restored to normal by the in vitro addition of sulfhydryl reagents such as dithiothreitol. Immunologic studies in several cases revealed the presence of nonfunctional enzyme protein, which crossreacted with anti-ALA-dehydratase antibody. 99.4.2.2 Molecular Aspects.  Molecular studies of ADP patients have identified nine-point mutations, two splice-site mutations, a two-base deletion, and

9

two different base changes at position -11 bp upstream of the exon 3 start site in the ALA-dehydratase gene (Human Gene Mutation Database; www.hgmd.org) (6,12,14,64). The parents in each case were not consanguineous, and the index cases had inherited a different ALA-dehydratase mutation from each parent. In addition, a point mutation, F12L, was identified in an asymptomatic Swedish girl who had 12% of normal erythrocyte ALA-dehydratase activity (64,65). The molecular basis of the ALAD2 polymorphism is a substitution of a lysine by an asparagine at residue 95 (K95N). To date, ADP has not been diagnosed prenatally, but this should be possible by determination of the ALA-dehydratase specific molecular lesions in cultured chorionic villi or amniocytes. 99.4.2.3 Clinical Manifestations.  The onset, severity, and clinical presentations of ADP are variable, presumably depending on the amount of residual ALAdehydratase activity. All patients had significantly elevated levels of plasma and urinary ALA, with little increase in PBG concentrations and ALA-dehydratase activities of 10% or less of normal. Four reported patients were male adolescents with symptoms resembling those of AIP, including abdominal pain and neuropathy (12–14). The third patient was an infant with more severe disease, including failure to thrive beginning at birth. The earlier age of onset and more severe manifestations in this patient reflect a more significant deficiency of ALA-dehydratase activity (64). Another patient was essentially normal until age 63, when he developed an acute motor polyneuropathy that was associated with a myeloproliferative disorder. This patient was heterozygous for an ALA-dehydratase mutation that presumably was present in erythroblasts that underwent clonal expansion due to the bone marrow malignancy (66). 99.4.2.4 Differential Diagnosis.  Lead, styrene, and succinylacetone (which is structurally similar to ALA and accumulates in hereditary tyrosinemia type 1 due to fumarylacetoacetase deficiency) inhibit ­ALA-dehydratase, causing increased urinary excretion of ALA and coproporphyrin, and clinical ­manifestations that resemble those of the acute porphyrias. Idiopathic acquired ALA-dehydratase deficiency has also been reported. Therefore, these known causes of ­ALA-dehydratase deficiency should be considered in the differential diagnosis of ADP and the diagnosis of ADP confirmed by demonstrating the underlying ALAdehydratase mutations. 99.4.2.5 Treatment.  Because of the small number of ADP patients, there is a limited experience in treatment. Glucose has shown little benefit. Hemin therapy has helped the clinical symptoms in patients with adolescentonset ADP (12,14,67) and was beneficial for preventing symptoms in one patient (12). A severely affected ADP child did not improve significantly with glucose, hemin, or liver transplant (13,64).

10

CHAPTER 99  Inherited Porphyrias

99.4.3 Acute Intermittent Porphyria Acute intermittent porphyria (AIP) is an autosomal dominant acute hepatic porphyria resulting from half-normal levels of HMB-synthase activity. The disease occurs in all ethnic groups with an estimated frequency of individuals with acute attacks of 1 to 2 per 100,000 in most European countries, making it the most common acute porphyria (3,23). It is estimated that less than 10% of individuals with an HMB-synthase mutation have acute attacks (3). A survey of 3350 healthy French blood donors identified two with HMB-synthase gene mutations for a frequency of 1 in 1750, indicating that clinical expression is low (3). The highly variable symptoms and signs include visceral, autonomic, peripheral, and central nervous system manifestations. Activation of the disease is clearly related to ecogenic factors, as its expression is usually triggered by hormonal, metabolic, dietary, or environmental factors, which can precipitate acute attacks. Symptomatic patients always have increased urinary excretion of the porphyrin precursors ALA and PBG. However, the great majority of heterozygotes with HMB-synthase deficiency remains clinically asymptomatic (“latent” or presymptomatic) and may never have increased urinary ALA and PBG excretions. 99.4.3.1 Biochemical Aspects.  The metabolic defect in AIP is the half-normal activity of HMB-synthase. For most HMB-synthase mutations, the enzyme activity is half-normal in all tissues. However, about 5% of patients have normal HMB-synthase activity in their erythrocytes (23) because they have mutations in or near exon 1 (see “Molecular Aspects” section). Moreover, the range of erythrocyte HMB-synthase activities in patients with classic AIP overlaps the range for normal individuals, as discussed later. Hepatic HMB-synthase activity in patients with active and latent AIP has not been ­compared. 99.4.3.2 Molecular Aspects.  To date, over 300 ­mutations have been identified, most being either point or splice-site mutations (Human Gene Mutation Database (www.hgmd.org) (6). Most are private, occurring in only one or a few unrelated families. Exceptions include W198X and R116W, which are common in the ­Swedish and Dutch populations, respectively and G111R, which was found in Argentinean AIP patients (68). A study of 143 Russian and Finnish AIP patients identified ­genotype-phenotype correlations (69). Based on the crystal structure of E. coli HMB-synthase, effects of specific AIP mutations on the human enzyme structure and ­function have been predicted (24,25). In a variant form of AIP, molecular studies have ­identified mutations that impair splicing of exon 1 to exon 3, thereby preventing the formation of the housekeeping but not the erythroid-specific transcript (1,6,23). Other exon 1 mutations alter the initiation of the translation codon, thereby precluding the translation of the housekeeping transcript (70). These tissue-specific

splicing and initiation of translation mutations provide an explanation for the deficient activity in the liver and other nonerythroid tissues in these cases, while the levels of HMB-synthase activity in erythrocytes remain normal. This variant form of AIP can be suspected in a patient with increased PBG, normal erythrocyte HMB-synthase, and laboratory findings that exclude HCP and VP, and mutation analysis is required for confirmation. Homozygous dominant AIP is a rare form of AIP in which patients have mutations in both of their HMBsynthase alleles and, therefore, very low (<2%) enzyme activity. The disease has been described in a Dutch girl, two young British siblings, and a Spanish boy (71,72). In these homozygous-affected patients, the disease presented in infancy with failure to thrive, developmental delay, bilateral cataracts, and/or hepatosplenomegaly. Interestingly, all these patients’ mutations (R167W, R167Q, and R172Q) were in exon 10 within 5 bases of each other. 99.4.3.3 Clinical Manifestations.  Acute intermittent porphyria is characterized by neurovisceral disturbances that develop after puberty in a minority of heterozygotes with HMB-synthase deficiency. Symptoms and signs are nonspecific and require a high index of suspicion to suggest the proper diagnosis (2). Abdominal pain, which is the most common symptom, is usually steady and poorly localized, but may be cramping, and is accompanied by nausea and vomiting. Constipation and signs of ileus, including abdominal distension and decreased bowel sounds, are common. However, increased bowel sounds and diarrhea may also occur. These abdominal manifestations are neurologic rather than inflammatory, and therefore tenderness, fever, and leukocytosis are generally absent or mild. Tachycardia, hypertension, restlessness, fine tremors, and excess sweating may be explained by sympathetic overactivity. Dysuria and bladder dysfunction are common, and urinary retention may require catheterization. Chronic hypertension and impaired renal function may develop over a long term. AIP is also commonly associated with mild abnormalities in liver function and the risk of more advanced liver disease and hepatocellular carcinoma is increased. Peripheral neuropathy in AIP is primarily motor and appears to result from axonal degeneration rather than demyelinization. However, paresis does not develop in all patients who suffer from acute attacks, even when abdominal symptoms are severe. Muscle weakness most commonly begins proximally, more often in the arms than in the legs. Tendon reflexes may be normal or hyperactive in early disease stages but are usually decreased or absent with advanced neuropathy. Paresis can be asymmetric and focal. Cranial nerves, most commonly the tenth and seventh, can be affected. Rarely, involvement of the optic nerves or occipital lobes may produce blindness. Extremity pain and paresthesia and areas of loss of sensation are indications of sensory involvement. Muscle weakness can progress to respiratory and bulbar

CHAPTER 99  Inherited Porphyrias paralysis and death, but this seldom occurs unless the porphyria is not recognized, harmful drugs are not discontinued, or appropriate treatment is not instituted. Sudden death, presumably due to cardiac arrhythmia, also may occur. Complete recovery even from severe neuropathy over a period of a year or longer is possible. Central nervous system involvement during acute attacks may be manifested as anxiety, insomnia, depression, disorientation, hallucinations, and paranoia and may suggest a primary mental disorder. Some patients have been mistakenly regarded as hysterical. Depression and other mental symptoms may be chronic in AIP patients. However, it has not been proved that the prevalence of AIP is higher in psychiatric patients than in the general population. Seizures may occur as part of the acute neurologic manifestations of AIP or as a result of hyponatremia, which have been observed and may result from a variety of causes, including inappropriate antidiuretic hormone (ADH) secretion, gastrointestinal losses secondary to vomiting and diarrhea, poor intake, or excess renal sodium loss. Antiseizure drugs are problematic because almost all have at least some potential for exacerbating AIP, with clonazepam being less likely to do so than phenytoin or barbiturates. Improved overall morbidity and mortality in acute porphyrias in the past 20 to 30 years is attributable to earlier detection, less use of barbiturates and sulfonamides in clinical practice, and better treatment of acute attacks (4). 99.4.3.4 Etiology and Pathogenesis.  Most of the ­factors known to precipitate acute porphyric attacks have the potential to induce the synthesis of ALAS1 in the liver, thereby increasing the accumulation of ALA, PBG, and other heme pathway intermediates. Normally, a half-normal amount of hepatic HMB-synthase activity is sufficient to avoid any accumulation of PBG. However, when certain environmental, metabolic, and hormonal factors increase the flux of ALA, PBG, and porphyrinogens through the pathway, the partially deficient activity of HMB-synthase may be insufficient to metabolize the increased amounts of PBG. The etiology of the neurologic manifestations in AIP is not established (73). The possibility that ALA or PBG might be neurotoxic is favored by the increased production of porphyrin precursors during acute porphyric attacks. ALA is taken up by most tissues more readily than PBG, which appears to more readily cross the blood–brain barrier. These intermediates may be converted in vivo to other substances, including porphyrins, which may have neurotoxic potential. The fact that AIP, HCP, VP, ADP, plumbism, and hereditary tyrosinemia are all associated with increased ALA and similar neurologic manifestations favors a neuropathic role for ALA. Moreover, ALA is structurally analogous to g-aminobutyric acid (GABA) and can interact with GABA receptors (73). Alternatively, deficient HMB-synthase activity could lead to a functional heme deficiency in the nervous

11

system, or predispose to unsaturation of hepatic tryptophan pyrrolase, thus leading to altered tryptophan delivery to nervous tissue. Experimental observations regarding these and other possible mechanisms for neurologic dysfunction in the acute porphyrias are reviewed in more detail, elsewhere (2,72,73). A mouse model in which HMB-synthase deficiency was introduced by gene targeting has been developed (74,75). These animals, when treated with a barbiturate, have impaired motor function, ataxia, increased levels of ALA in brain and plasma, and decreased heme saturation of liver tryptophan pyrrolase. Motor neuropathy can develop in these mice with normal or only slightly increased plasma or urinary ALA, suggesting a role for heme deficiency in nervous tissue (73,74). Studies of the brain MRIs of children with homozygous AIP have suggested damage primarily in white matter that was myelinated postnatally, while tracks that myelinated prenatally were normal (72). These findings suggest that a postnatal toxin such as elevated ALA or PBG rather than heme deficiency caused nervous tissue damage since prenatally elevated ALA and PBG would cross the placenta and be excreted in the mother’s urine. Also, the recent finding that a hepatic transplant cured a woman with AIP who had 37 acute attacks in 29 months pre-transplant supports the notion that the acute attacks result from the excess porphyrin precursors produced in the liver (76). 99.4.3.5 Precipitating Factors.  Certain clinical features of AIP suggest that endogenous steroid hormones are important precipitating factors (1). These include (i) the rarity of symptoms and excess porphyrin precursor excretion before puberty; (ii) more frequent clinical expression in women than in men; (iii) premenstrual attacks of the disease in some women and their prevention by gonadotropin-releasing hormone (GnRH) analogues; (iv) exacerbation of AIP due to exogenous steroids, such as oral contraceptive preparations; and (v) the presence of more subtle abnormalities in steroid hormone metabolism, such as a deficiency of hepatic steroid 5a-reductase activity. The latter can predispose to the excess production of steroid hormone metabolites that are inducers of hepatic ALAS1. 99.4.3.5.1 Pregnancy Is Usually Well Tolerated.  However, some women with AIP do experience an increased frequency of attacks during pregnancy. Earlier reports that worsening symptoms during pregnancy are more common may have been due in part to the use of barbiturates and perhaps to reduced caloric intake. Thus, pregnancy is not contraindicated in most women with AIP if harmful drugs are avoided and attention is given to proper nutrition. Drugs are an important cause of AIP attacks, and the avoidance of harmful drugs can favorably impact the disease course. The major drugs known or strongly suspected by most observers to be harmful in the acute porphyrias, as well as drugs that are known to be safe, are listed in Table 99-4 and include most anticonvulsants,

12

CHAPTER 99  Inherited Porphyrias

TA B L E 9 9 - 4    Some Major Drugs Considered Unsafe and Safe in Acute Porphyriasa Unsafe

Safe

Alcohol Barbituratesb Carbamazepineb Carisoprodolb Clonazepam (high doses) Danazolb Diclofenac and possibly other Ergots Estrogensb,d Ethchlorvynolb Glutethimideb Griseofulvinb Mephenytoin Meprobamateb (also mebutamateb, Methyprylon Metoclopramideb Phenytoinb Primidoneb Progesterone and synthetic progestinsb Pyrazinamideb Pyrazolones (aminopyrine, antipyrine) Rifampinb Succinimides (ethosuximide, methsuximide) Sulfonamide antibioticsb Valproic acidb

Acetaminophen Aspirin Atropine Bromides Erythropoietinb,c Gabapentin NSAIDsb Glucocorticoids Insulin Narcotic analgesics Penicillin and derivatives Ranitidineb,c Streptomycin tybutamateb)

NSAIDs, nonsteroidal anti-inflammatory drugs. aMore extensive list of drugs and their status are available in Anderson KE, Sassa S, Bishop DF, et  al. (2001) Disorders of heme biosynthesis: X-linked sideroblastic anemias and the porphyrias. In Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The Metabolic and Molecular Basis of Inherited Disease, 8th ed. McGraw-Hill, New York, p 2991; also see Web sites (www.porphyriafoundation.com; www.porphyria-europe.com). bPorphyria is listed as a contraindication, warning, precaution, or adverse effect in the U.S. labeling for these drugs. For drugs listed as unsafe, absence of such cautionary statements in the U.S. labeling does not imply lower risk. cAlthough porphyria is listed as a precaution in the U.S. labeling, these drugs are regarded as safe by other sources. dEstrogens have been regarded as harmful, mostly from experience with estrogen–progestin combinations and because they can exacerbate porphyria cutanea tarda (PCT). Although the evidence that they exacerbate acute porphyrias is weak, they should used with caution. Low doses of estrogen (e.g. transdermal) have been used safely to prevent side effects of GnRH analogues in women with cyclic attacks.

barbiturates, sulfonamide antibiotics, and metoclopramide. Other reviews and more extensive lists of drugs that are harmful or safe are published (1,2) or available through the American Porphyria Foundation Web site (www.porphyriafoundation.com) and the European Porphyria Initiative Web site (www.porphyria-europe. org). Most porphyrogenic drugs (e.g. barbiturates) exert their action by induction of hepatic ALAS1, cytochromes P450, and heme synthesis in the liver. Smoking

results in exposure to chemicals that induce cytochrome P450 enzymes and heme synthesis in the liver, and may increase the risk of attacks. A large retrospective study of risk from anesthetic use in AIP concluded that barbiturates or other inducing drugs are quite frequently detrimental in patients who have already displayed porphyric symptoms, but that they seldom exacerbate latent disease (77). Drugs are only rarely reported to cause acute symptoms in children, who have naturally low levels of endogenous hormones. Such observations indicate that attacks are likely to be due to the additive effects of more than one precipitating factor. Attacks can also be provoked by intercurrent infections and other illnesses and by major surgery. The mechanisms are not understood but may involve metabolic stress, impaired nutrition, and the increased production of steroid hormones and their ­ALA-synthase-inducing metabolities. A low caloric intake, usually instituted in an effort to lose weight, is a common contributing cause of acute attacks. Caloric or carbohydrate ­restriction can precipitate acute symptoms of AIP and increase ­porphyrin precursor excretion. Recent findings ­indicate that hepatic ALAS1 is regulated by the peroxisome ­proliferator-activated receptor g coactivator 1a ­(PGC-1a), which may represent an important link between nutritional status and acute porphyrias (78). 99.4.3.6 Laboratory Evaluations.  Urinary excretion of porphyrin precursors is markedly increased during acute attacks of AIP. Fecal porphyrins are usually normal or minimally increased in AIP, which helps to distinguish this disorder from HCP and VP. Because ALA and PBG are colorless, the reddish urine observed in AIP is due to increased porphyrins, which can form nonenzymatically from PBG. Brownish discoloration may be due to porphobilin, a degradation product of PBG, or dipyrrylmethenes. A normal result of a quantitative test for urinary PBG during a symptomatic period virtually excludes acute porphyria as a cause for concurrent symptoms. An exception is ADP, in which there is an increase in ALA, but not PBG (2). It is useful to follow ALA and PBG excretion in a symptomatic patient because the concentrations of these compounds generally decrease with clinical improvement. Such decreases are particularly dramatic after heme infusions. But, it is unusual for excretion of ALA and PBG to decrease to normal levels and remain normal unless the disease becomes clinically latent for a prolonged period. In contrast, ALA and PBG levels are often less elevated and may decrease to normal soon after acute attacks of HCP and VP. The diagnosis of AIP heterozygotes can be confirmed by the finding of half-normal levels of erythrocyte HMBsynthase. However, normal erythrocyte HMB-synthase activity does not exclude AIP, as some mutations in the HMB-synthase gene lead to a deficiency of the enzyme in the liver and other organs, but not in erythrocytes

CHAPTER 99  Inherited Porphyrias (1,78,79). A definitive diagnosis may also be precluded because of the following: (i) the normal range for erythrocyte HMB-synthase activity is wide (up to threefold) and low normal and high carrier values overlap; (ii) the enzyme activity is much higher in younger than older erythrocytes and therefore increases when erythropoiesis is stimulated; and (iii) improper processing, storing, and shipping of blood samples can decrease enzyme activity (2). The specific molecular defect in the HMB-synthase gene should be identified in each family in order to provide accurate diagnosis of presymptomatic AIP heterozygotes (2). Most HMB-synthase mutations are family-specific, with a few notable exceptions, where particular mutations have been transmitted over generations from single founders (1). Patients with AIP should have genetic counseling and be encouraged to inform family members about the disease and its genetics. Knowledge of genetic status enables family members to make informed decisions about lifestyle and to know the potential risks of certain drugs, preferably before the development of an acute illness. However, latent porphyria should not be construed as a health risk that limits health or life insurance. Prenatal diagnosis of AIP has been performed by enzymatic assay but is seldom indicated because the outlook for most carriers is favorable. 99.4.3.7 Treatment. 99.4.3.7.1 Supportive and Symptomatic Treatment.  Hospitalization may be required: for evaluation and treatment of severe pain, nausea, and vomiting; for administration of intravenous fluids, electrolytes, glucose, and hemin; and for close observation for electrolyte derangements and neurologic complications. Medications taken by the patient should be reviewed immediately and those identified as harmful stopped, if at all possible. Narcotic analgesics are usually required for abdominal pain, and small to moderate doses of a phenothiazine are indicated for nausea, vomiting, anxiety, and restlessness. Carbohydrate loading provides nutritional replacement, has some repressive effect on hepatic ALA synthase, but is less effective than hemin. It may suffice for mild attacks in patients with low narcotic requirements and without hyponatremia or paresis. Sucrose, glucose polymers, or carbohydrate-rich foods may be given to patients without abdominal distention and/or ileus and who can tolerate oral treatment. The standard intravenous regimen is 10% glucose for a total of at least 300–500 g daily. However, large volumes of 10% glucose may increase the risk of hyponatremia. Severe or prolonged attacks should be treated with hemin and may also require more nearly complete nutritional support. Tachycardia and systemic arterial hypertension may be treated cautiously with b-adrenergic blocking agents, but they may be hazardous in patients with hypovolemia, in whom increased catecholamine secretion may be an important compensatory mechanism (2). Seizures

13

are difficult to treat because almost all antiseizure drugs can exacerbate an attack. Gabapentin, and probably vigabatrin, can be given safely and benzodiazepines are relatively safe. Careful correction of hyponatremia and hypomagnesemia is important, particularly when associated with seizures. 99.4.3.7.2 Hemin Therapy.  Intravenous hemin addresses the underlying pathophysiology by repressing hepatic ALAS1, hence decreasing the overproduction of ALA and PBG. Hemin given intravenously at moderate dose (3–4 mg/kg day for 4 days) is mostly taken up in the liver, and can at least transiently replenish the depleted heme pool that regulates the synthesis of ALAS1. It cannot be given orally because it is catabolized by heme oxygenase during intestinal absorption. Hemin therapy should be started early (2). Although product labeling recommends an initial trial of intravenous glucose, hemin is the preferred therapy (80–82). The standard regimen is 3–4 mg of hemin per kilogram of body weight, infused intravenously once daily for 4 days. Hemin (Panhematin®), Lundbeck Pharmaceuticals, is available in the United States as lyophilized ­hydroxyheme (hematin) for reconstitution with sterile water just before infusion, and it is approved by the FDA for amelioration of acute porphyric attacks. Degradation products form rapidly in vitro when this product is reconstituted with sterile water, as recommended in product labeling, and these adhere to endothelial cells, platelets, and coagulation factors and cause a transient anticoagulant effect and often a phlebitis at the site of infusion. With repeated administration, phlebitis can compromise venous access. It is recommended that lyophilized hemin be reconstituted with human albumin to enhance stability (2). Another hemin preparation, heme arginate, is more stable in solution but is not available in the United States. Reconstitution of lyophilized hydroxyheme with albumin enhances stability of lyophilized hemin, decreases the incidence of phlebitis, and may enhance efficacy. Other uncommon reported side effects of hemin include fever, aching, malaise, hemolysis, a case of circulatory collapse that resulted in full recovery after subsequent hemin infusions, and one case of transitory renal failure after a dosage of 1000 mg. Experience indicates that hemin can be administered safely during pregnancy. Patients should be monitored closely during management of acute attacks for complications and signs of progression of acute porphyria such as electrolyte imbalance, acute psychiatric manifestations, muscle weakness, bladder retention, and ileus (2). Spirometry is sometimes indicated daily to detect respiratory impairment at least until the attack begins to resolve. Since patients with respiratory impairment can deteriorate rapidly, it is recommended they be placed in intensive care. ALA and PBG usually fall to normal whether therapy is started early or late, but this does not necessarily predict a clinical response.

14

CHAPTER 99  Inherited Porphyrias

Clinical improvement may occur within 1 to 2 days if hemin is started early in an attack. Patients can sometimes be discharged from the hospital within several days, although we recommend completion of the standard 4-day treatment course in the outpatient clinic. If initiated late, efficacy of hemin may not be immediately apparent because neuronal damage may already be advanced and slow to recover. In such cases, treatment for longer than 4 days should be considered, although the evidence that this improves the outcome is lacking. Hemin is seldom effective for chronic symptoms. Hemin therapy can be given in outpatient settings or in the home, if this facilitates prompt therapy and reduces medical care costs in patients with frequent attacks. Chronic renal failure has developed in some AIP patients and required renal transplantation. This may be caused by the development of chronic hypertension and prevented by control of blood pressure. AIP also increases the risk of chronic liver disease and especially hepatocellular carcinoma. These tumors seldom increase serum a-fetoprotein levels. Therefore, periodic screening by ultrasound or another hepatic imaging technique is recommended. 99.4.3.7.3 Transplantation.  An allogeneic liver transplant was performed on a 19-year-old female AIP heterozygote who had 37 acute attacks in the 29 months prior to transplantation. Posttransplantation, her elevated urinary ALA and BPG levels returned to normal in 24 hours, and she did not experience acute neurologic attacks for more than 18 months posttransplant (76). Two AIP patients had combined liver and kidney transplants secondary to uncontrolled acute porphyria attacks, chronic peripheral neuropathy, and renal failure, requiring dialysis. Both patients had marked improvement with no attacks and normal urinary PBG levels posttransplantation, as well as improvement of their neuropathic manifestations (83). It should be noted that liver transplantation is a high-risk procedure and should not be considered as an established treatment for acute porphyrias. Recently, liver-directed gene therapy has been proven successful in the prevention of drug-induced biochemical attacks in a murine model of human AIP (84). 99.4.3.8 Prevention of Acute Attacks and Later Complications.  Prevention of future attacks requires identifying precipitating factors. Educating the patient to avoid alcohol, smoking, and drugs that can induce exacerbations (see Table 99–4) is important, as in maintaining adequate nutrition. Lists of safe and harmful drugs are available (see previous discussion for references) but these are not infallible. Medical alert bracelets and wallet cards can help notify emergency medical personnel and ensure that unsafe drugs are not given to patients in emergencies. Some patients have frequent attacks even after exacerbating factors are removed, possibly because of unidentified modifier genes or environmental or endogenous precipitating factors. These patients should

be evaluated by a nutritionist and follow a well-balanced diet with sufficient calories to maintain weight. Gonadotropin-releasing hormone (GnRH) analogues can be highly effective for women with frequent cyclic attacks when symptoms are confined to the luteal phase of the menstrual cycle (1). The low-dose estrogen patch has been successful in reducing side effects when treatment beyond six months is contemplated. Gynecological examinations and bone density determinations are advised every 6 months during treatment. Continued need can be assessed every 1 to 2 years by stopping the treatment. Pregnancy increases levels of progesterone, a potent inducer of heme biosynthesis in the liver but nevertheless is well tolerated in most women with acute porphyria. For example, in a large series of women with AIP or VP who had 176 deliveries, porphyric symptoms were absent in 92% of their pregnancies (85). Because some women experience more frequent attacks during pregnancy, counseling women who wish to become pregnant must be individualized. Recurrent noncyclic attacks are sometimes prevented by weekly or biweekly infusions of single doses of hemin (3–4 mg/kg). Frequent treatment with hemin has a theoretic risk of iron overload (100 mg of hemin contains 8 mg of iron); therefore, serum ferritin levels should be monitored. In selected rare instances of severe, unremitting symptomatic disease, consideration might be given to orthotopic liver transplantation (76). Transplantation of hepatocytes or specific gene replacement therapy is a possible future therapeutic strategy.

99.4.4 Congenital Erythropoietic Porphyria Congenital erythropoietic porphyria (CEP), also known as Günther disease, is an autosomal recessive disorder due to the markedly deficient activity of URO-synthase, the forth enzyme in the heme biosynthetic pathway. CEP is panethnic, and as of 2000, about 160 cases were reported (28,86). 99.4.4.1 Biochemical Aspects.  The deficient activity of URO-synthase is the enzymatic defect in CEP. Affected homozygotes have markedly deficient, but not absent, URO-synthase activity, as sufficient enzyme is required to produce uroporphyrinogen III for normal (or even increased) rates of heme production. Most CEP patients have less than 10% of normal erythrocyte URO-synthase activity. The deficient URO-synthase activity leads to the accumulation of the substrate, hydroxymethylbilane (HMB), most of which is converted nonenzymatically to uroporphyrinogen I. Although uroporphyrinogen I can undergo decarboxylation by URO-decarboxylase to form hepta-, hexa- and pentacarboxyl porphyrinogen I and finally coproporphyrinogen I, further metabolism cannot proceed because the next enzyme in the pathway, COPRO-oxidase, is stereospecific for the III isomer.

CHAPTER 99  Inherited Porphyrias Therefore, the isomer I porphyrins are nonphysiologic, in that they cannot be metabolized to heme, and are pathogenic when they accumulate in large amounts and undergo auto-oxidizidation to their corresponding porphyrins. In patients with CEP, the large amounts of isomer I porphyrinogens that accumulate in bone marrow erythroid precursors (especially normoblasts and reticulocytes) and erythrocytes undergo auto-oxidation to the corresponding porphyrins, which damage erythrocytes, cause cutaneous photosensitivity, are deposited in tissues and bones, and are excreted in large amounts in the urine and feces. 99.4.4.2 Molecular Aspects.  The isolation and characterization of the URO-synthase cDNA and genomic sequences have permitted the identification of mutations in CEP patients (26,28,87). Over 39 mutations have been detected in unrelated CEP families including missense and nonsense mutations, large and small deletions and insertions, splicing defects, intronic branch point mutations, and erythroid-specific promoter mutations (6). Most mutations have been detected in only one or a few unrelated families, except for C73R, which has been found in about 33% of the alleles studied, L4F in 7%, and T228M in 6% (28). The recent discovery of alternative housekeeping and erythroid-specific promoters in the human URO-synthase gene facilitated the identification of four-point mutations within a 20-bp region of the erythroid-specific promoter in six unrelated CEP probands (26,88). These mutations included a −70T to C transition altering a GATA-1 binding element, a −76 G to A transition, a −86C to A transversion in three unrelated patients, and a −90C to A transversion that altered a putative CP2 binding element. These four pathogenic erythroid promoter mutations impaired erythroid-specific transcription, caused CEP, and identified functionally important GATA1 and CP2 transcriptional binding elements for erythroid-specific heme biosynthesis. To date, these are the only known promoter mutations in the erythropoietic porphyrias. For a review of URO-synthase mutations causing CEP, see (6,28). Genotype–phenotype correlations are possible in CEP once a patient’s mutations are known. Prokaryotic expression and gene promoter-reporter systems have been used to determine the in vitro levels of enzymatic activity expressed by the missense mutations and the promoter function of mutations in the erythroid-specific promoter. The prokaryotic expression of URO-synthase constructs containing missense mutations resulted in levels of enzymatic activity that ranged from essentially nondetectable to about 35% of the mean activity expressed by the wild-type allele in E. coli. The effect of the four promoter mutations on transcription also was assessed in vitro by determining the luciferase activity of each lesion using promoter-reporter gene constructs in uninduced and induced (with hemin) K562 erythroleukemia cells (88).

15

For genotype–phenotype correlations, a series of CEP patients were classified as very mild to severely affected, based on age, degree of hemolytic anemia, organomegaly, osteopenia, and cutaneous involvement (28). Homoallelism for the most common allele, C73R, was correlated with the most severe phenotype, nonimmune hydrops fetalis and/or transfusion dependency from birth. Consistent with the severe phenotype of C73R/C73R homozygotes, expression of the C73R allele in E. coli resulted in the detection of less than 1% of the activity expressed by the wild-type allele. The fact that the C73R/C73R homozygotes are viable and do not die early in fetal life indicates that the mutant enzyme retains a very small amount of residual activity that is sufficient to produce enough heme for the biosynthesis of hemoglobin and other essential hemoproteins. Alternatively, if the C73R mutation produced only nonfunctional or barely functional enzyme, then the fact that affected fetuses survive suggests the possibility of another gene that is responsible for URO-synthase activity during development. However, knockout mice homozygous for a null mutation in the URO-synthase gene died early in embryogenesis, indicating that the total deficiency of URO-synthase activity was an embryonic lethal (89). Patients heteroallelic for C73R and another mutation that expressed little residual activity, such as P53L, also resulted in a severe or moderately severe phenotype. Patients heteroallelic for mutations that expressed more residual activity such as A104V (7.7% of normal activity), A66V (14.5% of normal activity), and V82F (35% of normal activity) had milder forms of CEP, even if the other allele was C73R or another mutation that did not express detectable activity (e.g. nonsense and frameshift mutations). For example, a teenage boy whose genotype was C73R/A66V had only mild cutaneous involvement. Genotype–phenotype correlations for CEP probands with erythroid promoter mutations also have been made (88). For example, a proband heterozygous for a promoter mutation with low activity (–70C) and for C73R had the severe nonimmune hydrops fetalis phenotype, while a proband with the C73R mutation in one allele but with a promoter mutation with more activity (–76A) in the other allele had a mild cutaneous disease phenotype (88). As additional mutations are identified and expressed, more information will become available to evaluate genotype/phenotype correlations. Affected fetuses can be detected in utero by determining the uroporphyrin I levels in amniotic fluid, the URO-synthase activity in cultured amniotic fluid cells or chorionic villi, and/or by molecular analysis in families where the URO-synthase mutation(s) has been identified (90), or by a combination of these methods (91). 99.4.4.3 Clinical Manifestations.  The age at onset and clinical severity of CEP are highly variable, ranging from nonimmune hydrops fetalis due to severe hemolytic anemia in utero to milder, later-onset forms that have only cutaneous lesions in adult life (28,87). At least some

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CHAPTER 99  Inherited Porphyrias

of the late onset cases have been associated with myeloproliferative disorders, in which a clone of erythroid cells caries expresses URO-synthase deficiency (66). A number of factors are responsible for the phenotypic variability including (i) the amount of residual URO-synthase activity, (ii) the degree of hemolysis and consequent stimulation of erythropoiesis, and (iii) exposure to UV light. Therefore, as in other porphyrias, an interplay of environmental factors with the deficient enzyme activity determines the clinical expression of disease. Life expectancy may be diminished in more severely affected patients owing to the hematologic complications and the increased risk of infection (28). The major debilitating clinical features of CEP are photosensitivity and anemia. Severe cutaneous photosensitivity begins in early infancy and is manifested by increased friability and blistering of the epidermis on the hands and face and other sun-exposed areas. Skin manifestations resemble those of PCT, but with the much higher levels of porphyrins in plasma are usually much more severe. Bullae and vesicles contain serous fluid and are prone to rupture and infection. The skin may be thickened, with areas of hypo- and hyperpigmentation. Hypertrichosis of the face and extremities is often prominent. Recurrent vesicles and secondary infection can lead to cutaneous scarring and deformities, as well as to loss of digits and facial features such as eyelids, nose, and ears. Corneal scarring can lead to blindness. Porphyrins deposited in the teeth produce red fluorescence on exposure to long-wavelength UV light and a reddish-brown color in natural light, termed erythrodontia. Bone demineralization may result from expansion of the hyperplastic bone marrow and associated porphyrin deposition in bone (1,92). Hemolysis is accompanied by anisocytosis, poikilocytosis, polychromasia, basophilic stippling, reticulocytosis, increased nucleated red cells, decreased serum haptoglobin, increased unconjugated bilirubin, increased fecal urobilinogen, and increased plasma iron turnover, and probably results from the accumulated porphyrins in erythrocytes. Development of secondary splenomegaly may contribute further to the anemia and may also result in leukopenia and thrombocytopenia. The latter is sometimes associated with significant bleeding, and in such cases, splenectomy may be beneficial. Hemolytic anemia is especially severe if the bone marrow does not compensate, and some patients are transfusion dependent. For example, CEP-genotype C73R/C73R usually presents in utero with hemolysis and nonimmune hydrops, which if recognized can be treated by intrauterine transfusions. To better understand the pathophysiology and for studying treatment modalities, mouse models of CEP using knock-in techniques have been developed in which the mice have low URO-synthase activity and clinical symptoms, including erythrodontia, characteristic lightinduced cutaneous involvement, hepatosplenomegaly, and hemolytic anemia (93,94).

99.4.4.4 Laboratory Evaluation.  CEP should be suspected as a cause of nonimmune hydrops and in infants or young children with severe photosensitivity and markedly increased urinary and plasma porphyrins. Reddish urine in the diaper shortly after birth is often the first suggestion of this disease. Milder cases of CEP may be developed later in life in the presence of a myeloproliferative disorder and resemble PCT. Accumulation of isomer I porphyrins, especially uroporphyrin I and coproporphyrin I in bone marrow, erythrocytes, plasma, and urine is the biochemical hallmark of the disease. Urinary porphyrins are primarily uroporphyrin I and coproporphyrin I, the intermediate 7–, 6–, and 5–carboxyl porphyrins being excreted in excess as well. Although there is a great predominance of type I isomers, type III isomers are also increased. Protoporphyrin IX is sometimes the predominant porphyrin in erythrocytes in CEP, as in other autosomal recessive porphyrias. Urinary ALA and PBG are not increased. Fecal porphyrins are markedly increased, with a predominance of coproporphyrin I. URO-synthase activity can be measured in erythrocytes and cultured cells using either direct or coupled enzyme assays (95). CEP should be differentiated from other porphyrias with cutaneous photosensitivity. For example, HEP often mimics CEP clinically but is the homozygous dominant form of URO-decarboxylase deficiency. HEP is distinguishable from CEP by porphyrin patterns resembling PCT, including high levels of isocoproporphyrin in feces and urine and markedly decreased URO-decarboxylase activity in erythrocytes. Very rare homozygous forms of VP and HCP also may be characterized by photosensitivity in childhood and increased erythrocyte porphyrins. 99.4.4.5 Treatment.  Skin Protection. Protection of the skin from sunlight and minor trauma is essential. Sunscreen lotions and b-carotene are sometimes beneficial. Bacterial infections that complicate cutaneous blisters require timely treatment in an effort to prevent scarring and mutilation. Severe infections such as cellulitis and bacteremia may require intravenous antibiotics. 99.4.4.5.1 Marrow Suppression.  Frequent blood transfusions are sometimes essential for severe anemia. Transfusions repeated frequently enough to suppress erythropoiesis, and thereby decrease porphyrin production, can greatly reduce porphyrin levels and photosensitivity. Such therapy is likely to be successful if the hematocrit remains above 35% and deferoxamine is administered to reduce the resulting iron overload. Treatment with hydroxyurea to reduce the bone marrow porphyrin synthesis may be considered, especially after puberty when porphyrin production may increase (96). Splenectomy has substantially reduced transfusion requirements in some patients. Oral charcoal has increased fecal loss of porphyrins with milder disease, but seems less successful in more severe cases (97). Hemin therapy, which is effective for the treatment of the acute hepatic porphyrias, may be somewhat effective in CEP

CHAPTER 99  Inherited Porphyrias but has not been extensively studied. Chloroquine has not been beneficial. 99.4.4.5.2 Bone Marrow Transplantation.  Bone marrow transplantation (BMT) has proved curative for patients with CEP. To date, nine transplanted patients have been reported, and when successful, BMT has resulted in marked reduction in porphyrin levels and photosensitivity (for reviews, see (98,99)). The source of the hematopoietic stem cells has included bone marrow or umbilical cord blood from histocompatible sibs as well as from unrelated HLA-matched marrow. 99.4.4.5.3 Experimental Gene Therapy.  The success of BMT provides the rationale for hematopoietic stem cell gene therapy. The stable transduction of the patient’s own stem cells with vectors containing the URO-synthase cDNA would abrogate the need for HLA-identical donors and the risk of rejection. Various retroviral and lentiviral vectors expressing human UROsynthase have been used to transduce a variety of cell types including mononuclear cells derived from the bone marrow of normal and CEP subjects (100–106). Better transduction efficiencies were obtained with the lentiviral vectors than the retroviral vectors and all transduced cell types had increased URO-synthase activity and suppression of porphyrin accumulation. These studies are encouraging; however, in vivo efficacy of individual vector constructs may not be predictable from these in vitro experiments, and animal studies are needed. Such in vivo experiments could determine whether transduction of hematopoietic stem cells can be efficient enough to minimize the proportion of nontransduced progenitors capable of producing toxic quantities of porphyrins in their descendants.

99.4.5 Porphyria Cutanea Tarda Porphyria cutanea tarda (PCT) is caused by reduced activity of URO-decarboxylase, the fifth enzyme in the heme biosynthetic pathway. PCT is unique among the porphyrias as this cutaneous and biochemical phenotype results from an acquired, liver-specific enzyme inhibition in both sporadic (type I) and familial (types II and III) forms (1,34,107). PCT is the most common porphyria and has an estimated frequency of 1 per 25,000, of which ~80% have type I disease (34,107). This porphyria can also result from exposure to certain polyhalogenated aromatic hydrocarbons. The most notable occurrence of environmentally induced PCT was an outbreak in Turkey in the 1950s, caused by the ingestion of wheat treated with the fungicide hexachlorobenzene (HCB). 99.4.5.1 Biochemical Aspects. 99.4.5.1.1 Types I–III PCT Are Clinically Very Similar.  The enzymatic activity of hepatic URO-­ decarboxylase must be decreased by ~75% before porphyrins accumulate and clinical symptoms occur (34,107). However, the amount of hepatic UROdecarboxylase enzyme protein is not decreased below

17

its genetically determined level but is inhibited by a substance, not yet characterized, derived from a heme pathway intermediate (107). Production of the UROdecarboxylase inhibitor is iron-dependent. The multiple factors that can precipitate types I–III PCT act mostly be increasing hepatic iron content or oxidative stress (see later discussion). The genetically determined level of URO-decarboxylase in type II PCT is half-normal in all tissues, and the disease becomes manifested only when the hepatic enzyme becomes further reduced. 99.4.5.1.2 Type I Porphyria Cutanea Tarda.  In type I PCT, URO-decarboxylase activity is deficient in the liver and is normal in all other tissues such as erythrocytes. No URO-decarboxylase mutations have been identified in type I PCT. Moreover, there are no tissuespecific isoenzymes of URO-decarboxylase, and therefore, a mutation of the gene for this enzyme is unlikely to lead to a tissue-specific enzymatic deficiency. The tissuespecific enzymatic deficiency in type I PCT appears to be acquired because the amount of hepatic URO-decarboxylase protein, as measured immunochemically, is normal, suggesting that the enzyme has been inhibited, and with phlebotomy the enzyme activity gradually increases and both catalytic and specific activity may return to normal (108). URO-decarboxylase activity is not directly inhibited by iron. Considerable evidence suggests that type I PCT is caused by inhibition or inactivation of structurally normal URO-decarboxylase by a liver-specific, iron-dependent process that promotes the oxidation of uroporphyrinogen to uroporphyrin and a product that inhibits URO-decarboxylase. Efforts to isolate and characterize this inhibitor are currently in progress using laboratory models (107). 99.4.5.1.3 Type II Porphyria Cutanea Tarda.  In type II or familial PCT, the genetically determined level of URO-decarboxylase activity in all tissues is halfnormal due to the autosomal dominant inheritance of a URO-decarboxylase mutation. The half-normal amount of enzymatic activity is the product of the normal UROdecarboxylase allele. Half-normal enzyme protein and activity is demonstrated in nonhepatic tissues such as erythrocytes and cultured skin fibroblasts in clinically affected individuals and in family members with latent disease. However, manifest type II PCT develops only when hepatic URO-decarboxylase becomes reduced considerably below the inherited enzyme level, and to levels of activity corresponding to type I PCT (107). The amount of hepatic enzyme protein remains half-normal in type II PCT. URO-decarboxylase is not a rate-limiting enzyme for heme biosynthesis, and therefore most type II heterozygotes do not develop PCT unless precipitating factors are present (see later discussion) (107,109). 99.4.5.1.4 Type III Porphyria Cutanea Tarda.  Type III PCT is rare and is presumed to be inherited because more than one family member is affected. However, it resembles type I in that URO-decarboxylase

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CHAPTER 99  Inherited Porphyrias

activity is normal in extrahepatic tissues such as erythrocytes and URO-decarboxylase mutations have not been identified (108). Therefore, the genetic basis for this type of PCT is not yet understood, and it is not readily differentiated from type I. 99.4.5.1.5 Hepatoerythropoietic Porphyria.  Hepatoerythropoietic porphyria (HEP) is the homozygous dominant form of type II PCT. This disease is rare, as only about 30 cases from 24 families have been reported (110). The URO-decarboxylase mutations causing HEP often do not lead to complete loss of the enzyme activity, and some are CRIM-positive (29,111). The URO-decaboxylase activity in HEP patients has ranged from 3% to 28% of normal (29). 99.4.5.2 Genetic and Molecular Aspects.  UROdecarboxylase gene mutations are found only in type II PCT, as well as HEP. However, in types I and III PCT, other genetic as well as environmental factors (see later discussion) appear to contribute to the reduction of hepatic URO-decarboxylase in liver that is necessary for development of the clinically manifested disease. The half-normal activity of URO-decarboxylase in type II PCT is clearly inherited as an autosomal dominant trait. Over 100 mutations in the ­URO-decarboxylase gene have been identified, including over 50 mutations underlying type II PCT, and ten different missense mutations causing HEP (Human Gene Mutation Database; www.hgmd.org) (6). The ten mutations in the UROdecarboxylase gene identified in HEP include five such as G281E (112) that also have been found in type II PCT (29,31,110,113–116). HEP patients are either homoallelelic or heteroallelic for the URO-decarboxylase mutations. Of the URO-decarboxylase mutations listed in the Human Gene Mutation Database (6), 57.4% are missense, 0.7% nonsense, and 13.1% are splice-site mutations. Most URO-decarboxylase mutations have been identified in only one or two families. Exceptions include mutations g10insA (found in six Argentinean families) (111), G281E (found in 14 unrelated Spanish families) (112), and IVS6+1 (found in 6 unrelated families). Type III PCT has been studied in four Spanish families, in which at least two relatives had clinical manifestations of PCT with decreased URO-decarboxylase activity in liver but normal levels in erythrocytes and other tissues. To date, no mutations of the URO-decarboxylase locus have been detected in type III PCT. 99.4.5.3 Precipitating Factors.  A number of inherited and environmental factors contribute to the profound inhibition of hepatic URO-decarboxylase activity and the development of clinically manifested PCT. In type II PCT, the inheritance of a heterozygous URO-­decarboxylase mutation predisposes to the disease because the amount of enzyme is half-normal initially, and less inhibitor is required to develop overt PCT (107). Other inherited susceptibility factors include HFE mutations (C282Y and H63D) that increase iron retention, and possibly

polymorphisms of cytochrome P450 enzymes (117). Environmental and infectious factors include excess alcohol consumption, hepatitis C virus infection, HIV infection, estrogen use, smoking, decreased levels of antioxidants such as vitamins E and C, and carotenoids (3,107,108,118). These appear to ­contribute to development of PCT by increasing oxidative stress in hepatocytes and the production of an ­inhibitor of URO-­ decarboxylase. Multiple factors are present and may act in an additive fashion in the individual PCT patient (119). A study of 84 Swedish patients with PCT found that 23% of the patients had Type II PCT and 57% had hemochromatosis mutations, 14% of whom were homozygous for the C282Y mutation. Other risk factors included alcohol abuse (38% of males), estrogen treatment (55% of females), and antihepatitis C virus (29% of males) (120). Mutations in the hemochromatosis (HFE) gene may result in elevated tissue iron levels and therefore predispose to PCT. There are two common mutations causing hemochromatosis: the C282Y mutation causes hemochromatosis in homozygotes in northern Europeans and their descendents, and the H63D mutation, which is more common in southern Europe. One in ten normal individuals is a carrier of a HFE gene mutation and an increased frequency occurs in both sporatic and familial PCT patients (107,108,121). In American PCT patients, 63% to 73% had HFE mutations (119,122,123); in one series, 17 of 87 (19%) PCT patients were homozygous for C282Y compared with zero for the 56 controls (123). Among English PCT patients, 17% were found to be homozygous for the C282Y mutation and 20% were heterozygous (124). A review of eight studies (121) found a mutant hemachromatosis allele in 17% to 47% of patients with sporadic or familial PCT suggesting that the HFE gene is an important predispositional modifier gene for the clinical expression of PCT (121). 99.4.5.4 Porphyria Cutanea Tarda due to Halogenated Hydrocarbons.  In 1955 to 1958, an extensive outbreak of PCT occurred in eastern Turkey as a result of the ingestion of wheat treated with the fungicide HCB (1,108). Feeding of HCB to animals was subsequently shown to decrease hepatic URO-decarboxylase ­activity and to produce a porphyria biochemically ­similar to human PCT. Smaller case clusters have also been reported after exposure to other chemicals, including di- and trichlorophenols and 2,3,7,8-tetrachlorodibenzop-dioxin (TCDD, dioxin) (108). 99.4.5.5 Clinical Manifestations.  Skin lesions consist of fluid-filled vesicles and bullae on sun-exposed areas such as the dorsa of the hands and feet, the face, forearms, and legs. These may rupture, form crusted lesions, and heal slowly with residual scarring. Secondary infection may occur. Sun-exposed skin becomes friable, and minor trauma may precede the formation of bullae or may cause denudation of the skin. Small white plaques, termed milia, may precede or follow vesicle formation. Other cutaneous manifestations include hypertrichosis

CHAPTER 99  Inherited Porphyrias and hyperpigmentation, especially of the face, which can present in the absence of vesicles. Thickening, scarring, and calcification of affected areas of skin are sometimes striking and has been termed pseudoscleroderma because it resembles the cutaneous changes of systemic sclerosis. The skin lesions in PCT are generally indistinguishable from those in VP and HCP. PCT is commonly associated with evidence of chronic liver disease and sometimes with cirrhosis. Patients with PCT are also at risk to develop hepatocellular carcinoma; in several series, the incidence has ranged from 4% to 47%. These tumors appear as a complication of PCT and do not themselves contain or produce porphyrins in large amounts. They may result from longstanding liver damage in PCT, hemosiderosis, coexistent chronic hepatitis C infection, exposure to halogenated chemicals that are also carcinogenic, or to the effects of porphyrin deposition in the liver. PCT associated with advanced renal disease is often more severe and intractable than PCT occurring in its absence (1). HEP resembles CEP clinically and usually presents in infancy or childhood with onset of blistering skin lesions, hypertrichosis, scarring, and red urine. HEP is genetically heterogeneous, and unusually mild cases have been described (125). Two mild cases of HEP with only minor scarring have recently been described in two unrelated patients, one in a 5-year-old boy and the other in a 38-year-old man (110,126). Interestingly, both patients were homoallelic for the same mutation F46L, which resulted in less than 10% of normal URO-decarboxylase activity in these patients. 99.4.5.6 Laboratory Evaluation.  PCT is strongly suggested by the characteristic skin lesions in sun-exposed areas, especially on the backs of the hands. However, similar skin blistering is seen with other cutaneous porphyrias, with the exception of EPP. The most useful initial diagnostic test is a total plasma porphyrin determination. A normal plasma porphyrin level excludes PCT, whereas a high level with a fluorescence emission maximum at neutral pH near 619 nm excludes VP and is highly suggestive of PCT (108). Measurements of urinary and fecal porphyrins provide confirmation of PCT. URO-decarboxylase activity can be measured in erythrocytes and lymphoblasts (89) and can be used to ­distinguish Types I and II since Type 1 PCT patients will have normal levels of erythrocyte URO-decarboxylase, while Type II PCT patients will have ~50% of normal levels (15). Molecular analysis more reliably diagnoses type II patients by identifying the underlying UROdecarboxylase gene mutations (127). Porphyrins are increased in the liver, plasma, urine, and stool in PCT (63). A slight increase in ALA is noted in some patients, but PBG excretion is normal. ­Urinary porphyrins consist mostly of uroporphyrin and ­7-carboxyl porphyrin, with lesser amounts of ­coproporphyrin and 5- and 6-carboxyl porphyrins. The excess urinary uroporphyrin in PCT is predominantly

19

isomer I; 7- and 6-carboxyl porphyrins are mostly isomer III; and ­5-carboxyl porphyrin and coproporphyrin are approximately equal mixtures of isomers I and III. The finding of increased isocoproporphyrins, most readily demonstrated in feces, is diagnostic for a deficiency of URO-decarboxylase (34). These unusual 4-carboxyl porphyrins are produced when hepatic UROdecarboxylase is deficient, because 5-carboxyl porphyrinogen III, which accumulates in PCT, can be metabolized by COPRO-oxidase to yield dehydroisocoproporphyrinogen. This porphyrinogen is excreted in bile and undergoes auto-oxidation and side-chain modification by bacterial enzymes in the intestine to give isocoproporphyrin and deethylisocoproporphyrin, the major representatives of the isocoproporphyrin series in the feces of PCT patients. Increased liver porphyrins are composed mostly of uroporphyrin and 7-carboxyl porphyrin. The biochemical findings in HEP are similar to those in other forms of PCT. In addition, the concentration of protoporphyrin in erythrocytes is increased and is predominantly zinc protoporphyrin. 99.4.5.7 Therapy.  The diagnosis of PCT should be firmly established by biochemical investigations before treatment is initiated, because VP and HCP can produce similar cutaneous lesions but are unresponsive to measures that are highly effective in PCT. Imaging studies are advisable to exclude complicating hepatocellular carcinoma and to serve as a baseline for follow-up. Testing for known precipitating factors is recommended to include hepatitis C and HIV infections. Patients should abstain from alcohol, estrogens, iron supplements, or other exogenous agents that may exacerbate the disease. Drugs such as barbiturates, phenytoin, and sulfonamides that are harmful to patients with acute porphyrias are seldom reported to contribute to the clinical expression of PCT, but should be avoided as a precaution. Standard therapy consists of repeated phlebotomy, which can produce remission in almost all patients (1). The aim is to gradually reduce excess hepatic iron by removing about 450 mL of blood at intervals of 1 to 2 weeks until the serum ferritin reaches the lower limits of normal (108). Plasma (or serum) porphyrin levels decrease in parallel and become normal within 1 to 2 months after the target ferritin concentration is achieved. Hemoglobin or hematocrit levels should be followed closely to prevent the development of symptomatic anemia. Continued phlebotomies are seldom needed even if ferritin levels later return to normal. However, it is advisable to follow porphyrin levels and reinstitute phlebotomies if porphyrin levels begin to rise. Even cutaneous scarring and pseudoscleroderma can improve with phlebotomy and serum markers for the liver cell function to normalize (108). Recombinant erythropoietin is an effective treatment and can support phlebotomy therapy when PCT is associated with end-stage renal disease (1). Small doses of chloroquine (125 mg twice weekly) or hydroxychloroquine (100 mg twice weekly) are also

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CHAPTER 99  Inherited Porphyrias

effective in producing remissions of PCT (127). These drugs promote excretion of accumulated porphyrins in the liver in PCT, possibly by complexing with porphyrins. However, the standard antimalarial doses of these drugs may induce acute hepatic damage, nausea, vomiting and fever, and elevated urinary and plasma porphyrin levels due to the release of large amounts of stored porphyrins from the liver (1). There may be a transient increase in photosensitivity. Such side effects are minimal or absent with much lower doses. This treatment is sometimes combined with repeated phlebotomy (108). Prospective study comparing these two forms of therapy is lacking.

99.4.6 Hereditary Coproporphyria Hereditary coproporphyria (HCP) is an acute hepatic porphyria and results from the deficient activity of COPRO-oxidase, the sixth enzyme in the heme biosynthetic pathway. HCP is inherited as an autosomal dominant trait due to COPRO-oxidase mutations, whose clinical expression is influenced by ecogenic and metabolic factors. This condition is less frequent than AIP or VP (40). Clinical symptoms rarely occur before puberty and are very similar to AIP with the exception of photosensitivity, which can develop in HCP patients but much more rarely than in VP (1). Certain mutations in the COPRO-oxidase gene, such as K404E, when present in either the homozygous or compound heterozygous states produce a biochemical variant called harderoporphyria, characterized by increased fecal levels of a tricarboxylic porphyrin, harderoporphyrin (41,129). Cases of homozygous HCP have also been reported (42,43). 99.4.6.1 Biochemical Aspects.  The activity of the mitochondrial enzyme COPRO-oxidase is about 50% of normal in cultured fibroblasts, circulating lymphocytes, and leukocytes from HCP heterozygotes. In one case of homozygous HCP, the residual COPRO-oxidase activity (approximately 2% of normal) had a normal Km value. By contrast, in three cases in a family with harderoporphyria, the mutant enzyme exhibited increased thermostability and reduced affinity for both harderoporphyrinogen and coproporphyrinogen III, which is consistent with a structurally altered enzyme. 99.4.6.2 Molecular Aspects.  Over 40 mutations in the COPRO-oxidase gene are listed in the Human Gene Mutation Database, including missense, nonsense, splice-site, and small insertion or deletion mutations (Human Gene Mutation Database; www.hgmd.org) (6,130). Most have been identified in only one family (40). In a study of 17 unrelated British HCP patients, only one mutation, 1277GÆA, which causes exon 6 skipping was found in more than one patient (131). No ­genotype–phenotype correlations have been observed in HCP (131). Five single nucleotide polymorphisms were identified in the COPRO-oxidase gene, but none appear to play a major role in clinical expression of HCP (132).

Studies of the human COPRO-oxidase crystal structure and a hydrophobic cluster analysis method indicated that only missense mutations in amino acids positions 400–404 in exon 6 resulted in harderoporphyria. In fact, mutation K404E is found either homoallelic or heteroallelic in all patients with harderoporphyria studied, to date. The amino acids in this region appear to be involved in retaining harderoporphyrinogen for the second decarboxylation step whereas mutations in these amino acids lead to the release of the porphyrinogen intermediate (39,41). 99.4.6.3 Clinical Manifestations.  The neurovisceral symptoms of HCP are identical to those of AIP; however, the disease is probably less severe than AIP, and only a few patients have been reported to die from respiratory paralysis. Photosensitivity similar to that in PCT and VP sometimes occurs. In one series of 50 patients, the most common clinical manifestations were abdominal pain (80%), vomiting (34%), skin lesions (29%), neuropathic involvement (23%), psychiatric symptoms (23%), and constipation (20%) (40). In a study of 53 German HCP patients during acute manifestations, 89% had abdominal pain, 33% had neurologic symptoms, 28% had psychiatric symptoms, and 25% had cardiovascular symptoms, while only skin photosensitivity was observed in only 5% (114). In 69% of these patients, the abdominal pain occurred without other neurologic manifestations, while 27% of the patients had both abdominal and other neurologic symptoms; 4% had only neurologic symptoms (114). HCP can be exacerbated by many of the same factors that cause attacks in AIP, including drugs such as barbiturates and endogenous or exogenous steroid hormones. The disease is latent before puberty, and symptoms are more common in adult women than in men. Hepatitis and other superimposed liver diseases in an HCP patient can increase porphyrin retention and photosensitivity. Patients with homozygous HCP, including some with harderoporphyria, developed symptoms in early childhood. Manifestations have included jaundice, severe hemolytic anemia with splenomegaly, and compensatory hyperactive bone marrow (43,133). 99.4.6.4 Laboratory Evaluation.  A common and ­characteristic biochemical change in HCP is a large, isolated increase in fecal coproporphyrin, predominantly isomer III (40). Feces of symptomatic heterozygotes have a 10-fold to 200-fold increase in coproporphyrins and little or no increase in protoporphyrin. An increase in the ratio of coproporphyrin III to coproporphyrin I in feces is useful for diagnosis of both active and latent HCP. Increased urinary excretion of ALA, PBG, and total porphyrins (mostly uroporphyrin III and coproporphyrin III) is observed during acute attacks (114). With resolution of symptoms, ALA and PBG levels revert to normal more readily in HCP (and VP) than in AIP, and HCP patients in nonacute stages may show only increases of urinary and fecal porphyrins. For

CHAPTER 99  Inherited Porphyrias example, in a series of 53 German HCP patients, the average total urinary porphyrins during acute phases was 29,905 nmol/24 hr (6 patients) and around 1100  nmol/24 hr during subclinical and latent phases (average of 47 patients); normal levels were <224 nmol/24  hr (113). Total fecal porphyrins were 5508 nmol/g dry weight at active stages of HCP, compared with 1730 and 694 nmol/g dry weight (normal <224 nmol/g dry weight) in subclinical and latent phases, respectively. However, the percentage of the fecal coproporphyrin III isomer was still elevated in the patients in the subclinical and latent phases (114). Porphyrin excretion patterns in homozygous HCP resemble those observed in heterozygotes but reflect a more profound enzymatic deficiency. Harderoporphyria is characterized by a marked increase in fecal excretion of harderoporphyrin as well as coproporphyrin. In one patient with harderoporphyria, 90% of the porphyrins in his feces were in the form of harderoporphyrin (129). COPRO-oxidase activity can be measured in mononuclear cells (134). Individuals with a mutation in one of their COPRO-oxidase alleles have about 50% of normal activity in mononuclear cells. For screening family members, measurement of fecal porphyrins may be useful, especially if the ratio of coproporphyrin isomers I and III is determined; however, asymptomatic adults and children with the enzymatic deficiency may not excrete excess porphyrins. 99.4.6.5 Therapy.  Acute attacks of HCP are treated in the same manner as in AIP (2). Hemin (lyophilized hydroxyheme or heme arginate) therapy is helpful in treating acute attacks of HCP (40). Cholestyramine may be of some value for photosensitivity occurring with liver dysfunction, but phlebotomy and chloroquine are not effective.

99.4.7 Variegate Porphyria VP is an autosomal dominant hepatic porphyria resulting from the deficient activity of PROTO-oxidase, the seventh enzyme in the heme biosynthetic pathway. The disorder is described as variegate because it can present with neurologic manifestations, photosensitivity, or both. The clinical penetrance of VP in adults is estimated at ~40% (135–137). In most countries, VP is less common than AIP, with the notable exception of South Africa, where 3 of every 1000 white persons have inherited VP. This high prevalence is due to a founder effect from a Dutch couple who immigrated to South Africa in 1688, one of whom carried a specific PROTO-oxidase mutation (133). A number of cases of homozygous dominant VP have also been described (49,50,138–141). 99.4.7.1 Biochemical Aspects.  PROTO-oxidase activity is approximately half-normal in cultured skin fibroblasts and lymphocytes from VP patients. Because PROTO-oxidase is a mitochrondrial enzyme, it is not present in mature erythrocytes. Assays for

21

PROTO-oxidase in lymphocytes or cultured cells are difficult and are not widely available for diagnosis and family screening (136). Protoporphyrinogen IX, the substrate for PROTOoxidase, accumulates in patients with VP and undergoes auto-oxidation to protoporphyrin IX, which is characteristically increased in VP. A close functional association between PROTO-oxidase in the inner mitochondrial membrane and COPRO-oxidase in the intermembrane space may relate to the excess excretion of both protoporphyrin IX and coproporphyrin III in this disease. 99.4.7.2 Molecular Aspects.  Around 150 mutations in the PROTO-oxidase gene have been identified in patients with VP including missense, nonsense, splice site, and small deletions and insertions (Human Gene Mutation Database; www.hgmd.org) (6,136). The missense mutation, R59W, is the common mutation in most South Africans with VP of Dutch descent (133). In 108 unrelated English and French VP patients, 66 ­mutations were identified; most were found in only one or two unrelated families, but five (L15F, E198X, L295P, 1082insC, and Q435X) had frequencies of 7% to 12% (142). No ­genotype/phenotype correlations were identified. In 21 ­Finnish VP families, the common missense mutation R152C was identified in 11 (52%), while the missense mutation I12T was found in two large families (9.5%) (137). Of interest, none of the patients with the I12T mutation had photosensitivity, only one had an acute attack, and all had lower levels of porphyrins than patients with mutation R152C (137). Mutations have also been identified in patients with the rarer ­homozygous dominant form of VP (48,49,138–141). Most have some residual enzymatic activity, allowing for synthesis of heme in amounts sufficient for many essential hemoproteins. 99.4.7.3 Clinical Manifestations.  Clinical expression of VP before puberty is rare; the disease may even present late in life (143). VP can present with skin photosensitivity, acute neurovisceral crises, or both (47). In two large studies of VP patients from Europe and South Africa, 59% had only skin lesions, 20% had only acute attacks, and 22% had both (142). Among Finnish VP patients, the frequency of skin symptoms was 40% and acute attacks 27% (137). Interestingly, the proportion of Finnish patients with acute attacks decreased from 38% to 14% among patients diagnosed before and after 1980, while the proportion with skin symptoms remained similar. The reasons for the decline in symptoms are unclear (137). A similar decline in the frequency of acute attacks, from 38% before 1980 to 4% in 2004, was observed among South African VP patients, presumably due to increased detection and counseling of heterozygotes to avoid use of acute attack-inducing drugs, steroids, and dieting (135). The neurovisceral manifestations of abdominal pain, vomiting, constipation, hypertension and tachycardia, and peripheral neuropathy are indistinguishable from those of AIP and HCP. Skin manifestations are very

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CHAPTER 99  Inherited Porphyrias

similar to those of PCT and HCP, are usually of longer duration, and may occur apart from the neurovisceral symptoms. Photosensitivity is more common than in HCP. Drugs, steroids, and nutritional factors that are detrimental in AIP can also provoke exacerbations of VP (1,2). Photosensitivity may be less commonly associated with VP in more northern countries, where sunlight is less intense (136). Patients with homozygous dominant VP have the early onset of symptoms, severe photosensitivity, absence of acute attacks, and elevated erythrocyte zinc protoporphyrin levels (49). In some cases, neurologic symptoms and developmental disturbances, including growth retardation, were noted in infancy or childhood. One homozygous VP patient had severe photosensitivity and mild sensory neuropathy and over a 20-year period developed IgA nephropathy (48). The heterozygous parents of these patients had approximately half-normal enzyme activity as expected. 99.4.7.4 Laboratory Evaluation.  Fecal protoporphyrin and coproporphyrin and urinary coproporphyrin are markedly increased in clinically expressed VP. Urinary and fecal coproporphyrin is mostly type III. Urinary ALA, PBG, and uroporphyrins are increased during acute attacks but may be normal or only slightly increased during remission. ALA and PBG may be less elevated and return to normal more rapidly in VP and HCP than in AIP. Plasma porphyrins, consisting in part of a dicarboxylate porphyrin tightly bound to plasma proteins, are increased in VP particularly when photosensitivity or other symptoms are present. The fluorescence emission spectrum of plasma porphyrins at neutral pH in VP is characteristic and can distinguish this disease from other types of porphyria, especially PCT: the emission maxima occurs at 626 nm in VP; 619 nm in PCT, CEP, HCP, and AIP; and 634 nm in EPP (63). This method of measuring plasma porphyrins is perhaps the most sensitive method of detecting latent cases of VP, other than measuring PROTO-oxidase in lymphocytes or detecting a specific mutation by molecular methods. VP can be distinguished from HCP by fecal and plasma porphyrin analyses. Assays for PROTO-oxidase are difficult, since the enzyme is not present in erythrocytes and are not widely available for diagnostic and family screening (63). Mutation analysis is preferred for confirming the diagnosis and detecting heterozygous relatives. 99.4.7.5 Therapy.  Glucose, hemin, and other measures employed in AIP are recommended for the treatment of acute attacks of VP (2,47,136). Other therapies such as propranolol, d-penicillamine, hemodialysis, alkalization of urine, and b-carotene are of little or no benefit. Repeated venesections and chloroquine are not effective for skin manifestations in VP, even though these appear identical to those of PCT. Measures to protect the skin from sunlight with appropriate clothing and opaque sunscreen preparations are useful. Exposure to short-wavelength UV light, which does not excite

porphyrins, may provide some protection by increasing skin ­pigmentation.

99.4.8 Erythropoietic Protoporphyria Erythropoietic protoporphyria (EPP) is due to the partially deficient activity of ferrochelatase, the last enzyme in the heme biosynthetic pathway (1,57). EPP also has been termed erythrohepatic protoporphyria and protoporphyria. EPP is the most common erythropoietic porphyria and, after PCT and AIP, is the third most common porphyria. EPP is an autosomal dominant disease in most affected families. However, many EPP patients had only 10% to 30% of normal ferrochelatase activity instead of the expected 50% of normal activity. Recently, it was shown that an intronic polymorphism in the wild-type allele reduces its expression, accounting for the lower level of enzymatic activity. EPP is therefore an autosomal dominant porphyria in which a low-expression polymorphism predisposes to clinical expression (penetrance) (134). The presence of the intronic polymorphism and the nature of the other mutation (e.g. null vs. missense) may be responsible in part for the penetrance and variable expressivity of this disease. In some families, the pattern of inheritance is autosomal recessive, with affected individuals inheriting a coding region mutation from each parent (144). Although the disease is most common in whites, it does occur in persons of other races, including blacks. The low expression polymorphism is found in ~10% of the normal white population and is also common in Asians but is rare in Africans (58). Recently, deletions in exon 11 of the ALAS2 gene have been described, which cause an X-linked protoporphyria (XLP) which is clinically indistinguishable from EPP. The deletion of the c-terminal amino acids of ALSA2 results in increased ALAS2 activity and the accumalation of protoporphyrin (145). XLP accounts for approximately 2% of cases with the EPP phenotype (146). 99.4.8.1 Biochemical Aspects.  Partially deficient ­ferrochelatase has been documented in bone marrow, reticulocytes, liver, cultured fibroblasts, and blood or leukocytes from patients with EPP (1). The deficient enzyme activity becomes rate-limiting for protoporphyrin conversion to heme primarily in bone marrow reticulocytes. Ferrochelatase activity in tissue lysates of EPP patients has been reported to be as low as 10% to 30% of normal, which is much less than the 50% of normal activity that would be expected if EPP were inherited as an autosomal dominant enzymopathy. In a study of French and Swiss EPP patients, ferrochelatase activity ranged from 15% to 50% of normal (147). In a recently described variant form of EPP, ferrochelatase activity was normal, and an abnormality in iron delivery to the normal enzyme was postulated (148). 99.4.8.2 Molecular Aspects.  To date, over 100 mutations in the ferrochelatase gene have been identified that cause EPP (Human Gene Mutation Database;

CHAPTER 99  Inherited Porphyrias www.hgmd.org) (6,147) including nonsense, missense, splice-site mutations, nonsense, and insertions/deletions or rearrangement mutations. Based on the type of mutation, about 75% of lesions result in an unstable or absent protein (null alleles). It has been suggested that there are genotype–phenotype correlations between mutations that result in unstable proteins (null) and liver complications in EPP patients. A study of 112 EPP patients with known ferrochelatase mutations found that all 18 EPP patients with severe liver complications had “null” alleles, while none of the 20 patients who had missense mutations developed liver complications (149). Another study of 31 EPP patients found that all 15 EPP patients with liver disease had null mutations (splicing, nonsense, or frameshift mutations), while 50% of the 16 patients who had only photosensitivity had missense mutations (150,151). Mutation analysis of 105 English EPP patients identified three typical EPP patients with homozygous EPP, having two different mutations and one who was homoallelic for a missense mutation (152). The phenotypes of these homozygous EPP patients were very similar to EPP patients with one disabling mutation and the low expression intron 3 polymorphism, but their low ferrochelatase activity increased their risk for liver disease (152). In XLP, the erythrocyte protoporphyrin levels appear to be higher than other forms of EPP, and the proportions of free and zinc protoporphyrins are approximately equal. 99.4.8.3 Genetic Aspects.  As noted previously, many EPP patients have about 20% to 30% of normal ferrochelatase activity rather than the 50% expected if the EPP was inherited as a simple autosomal dominant trait. Recent studies have shown that the presence of a polymorphism in intron 3 of the normal ferrochelatase allele affects the level of ferrochelatase activity and the severity of EPP. When the normal allele has a C at position -48 of intron 3, a cryptic acceptor splice site is activated, resulting in the insertion of 63 bp of the intron into the coding sequence (134). The IVS3-48C mRNA transcript contains a new stop codon and is rapidly degraded. The IVS3-48C polymorphism was present in ~10% of normal European individuals, 43% of normal Japanese, 31% of normal southeast Asians, and <1% of normal black West Africans (58,134,152). Transfection studies showed that the IVS3-48C construct produced ~40% aberrantly spliced mRNAs, while the common IVS348T construct produced only 20% aberrantly spliced mRNAs (134). In studies of 40 unrelated European and 31 American symptomatic EPP patients, 95% (38 of 40) and 94% (29 of 31), respectively, had the IVS3-48C allele (132,150). Of note, none of 12 asymptomatic individuals with ferrochelatase mutations had the IVS3-48C allele (151). Additional studies of 113 overt French EPP patients and 61 asymptomatic carriers showed that none of the asymptomatic carriers had the IVS3-48C allele while 93 of 95 overt patients did (58). The EPP patients with the

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IVS3-48C allele had lower levels of ferrochelatase activity than individuals with the IVS3-48T allele. These studies and others (150,153–155) indicate that symptomatic disease in most EPP patients is the result of a mutation in one ferrochelatase allele that alters markedly the structure, stability, and activity of the enzyme protein and a low expressing normal ferrochelatase allele, which is caused by the presence of the IVS3-48C polymorphism. Therefore, it appears that in most families the presence or absence of the IVS3-48C allele determines which individuals will be symptomatic. In patients who do not have the IVS-48C polymorphism, it is possible that their reduced ferrochelatase activities result from the fact that the enzyme is a homodimer, and the dimerization of mutant and wildtype polypeptides may reduce the total activity. Recent studies of recombinant human wild-type and mutant ferrochelatase, expressed in E. coli, confirmed that ferrochelatase functions as a dimer and indicated that, for some mutations, the dimeric enzymes containing only mutant or mutant and wild-type heterodimers may be unstable or have markedly reduced activity (50,156). Mouse models of EPP (157,158) may help further clarify the lower than expected ferrochelatase activity in EPP patients. In these models, the different genetic backgrounds or the absence of the heme-regulated eIF2a kinase (HRI) can effect the clinical severity of EPP (157,159). In XLP, to date, only two ALAS2 mutations, all deletions of 1 to 4 bases, have been described, which markedly increase ALAS2 activity (145). 99.4.8.4 Etiology and Pathogenesis.  Porphyrins absorb light maximally at wavelengths near 400 nm (the Soret band) and enter an excited energy state that is manifested by fluorescence and, in the presence of molecular oxygen, by the formation of singlet oxygen and other oxygen species that can produce tissue damage. As might be expected, the skin is maximally sensitive to 400-nm light in EPP. Light-induced tissue damage may be accompanied by lipid peroxidation, oxidation of amino acids, and crosslinking of proteins in cell membranes. Histologic changes, predominantly in the upper dermis, may include amorphous material deposited around blood vessels and may resemble the findings in PCT. Immediate light-induced damage to capillary endothelial cells in the upper dermis has been described in EPP. Circulating erythrocytes are an insufficient source for the excess protoporphyrin produced and excreted in EPP, and the presence of brightly fluorescent immature erythroid cells in the bone marrow of EPP patients presumably is a major source of the excess protoporphyrin (57). The liver also may be a source for some of the accumulated protoporphyrin (108); however, the relative contribution of hepatic and erythroid sources of the excess protoporphyrins is unclear. Studies in an EPP mouse model showed that bone marrow cells from a wild-type animal when transplanted into an irradiated EPP animal corrected the photosensitivity and fatal liver

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CHAPTER 99  Inherited Porphyrias

disease, suggesting that the bone marrow was the major site for the excess protoporphyrins (160). In the reverse experiment, transplanting EPP bone marrow cells into irradiated normal mice resulted in protoporphyria (38% of erythrocytes contained flurorescent protoporphyrins), but not in liver disease, suggesting that the absence of ferrochelatase activity in the liver is a necessary component for development of EPP-associated liver disease (161). The normal recipients of EPP bone marrow cells also showed minimal skin photosensitivity despite high levels of plasma and erythrocyte protoporphyrins, suggesting that normal ferrochelatase activity in skin prevented photosensitivity (161). Free protoporphyrin in EPP binds less readily to hemoglobin than does zinc protoporphyrin and diffuses more rapidly into the plasma. Moreover, UV light may cause free protoporphyrin to photodamage its ­hemoglobin-binding site and thus be released from the erythrocytes, even without disruption of the cell ­membrane. Protoporphyrin may then diffuse into the plasma, where it is bound to albumin. This light-mediated mechanism for the release of free protoporphyrin from hemoglobin in EPP may be important because binding of excess free protoporphyrin to hemoglobin is usually greater than binding to plasma proteins. Most of the protoporphyrin in erythrocytes is found in a small percentage of cells, and the rate of protoporphyrin leakage from these cells is proportional to their protoporphyrin concentration. The capacity of the liver to take up and excrete protoporphyrin into bile may also influence the flux of protoporphyrin from erythroid cells to the plasma. In uncomplicated cases, hemolysis is uncommon or very mild. However, mild anemia with hypochromia and microcytosis or mild anemia with reticulocytosis is sometimes noted (144). Depletion of iron stores may be relatively common even in the absence of iron-deficiency anemia in EPP. Iron accumulation in erythroblasts and ring sideroblasts occur in some EPP patients. Patients with EPP have high concentrations of protoporphyrin in bile and seem predisposed to develop gallstones that are fluorescent and composed at least in part of protoporphyrin. Protoporphyrin is cholestatic when infused intravenously in rodents. The potentially life-threatening hepatic complications of EPP are often preceded by increasing levels of erythrocyte and plasma protoporphyrin, abnormal liver function tests, and marked deposition of protoporphyrin in liver cells and bile canaliculi. 99.4.8.5 Clinical Manifestations.  A major clinical ­feature of EPP is cutaneous photosensitivity, which usually begins in childhood. Photosensitivity is associated with substantial elevations in erythrocyte protoporphyrin and occurs only in patients with a genotype that results in ferrochelatase activity below ~35% of normal (3,108). Protoporphyrin levels remain quite constant over time, although cutaneous symptoms are generally more troublesome in the spring and summer when

sunlight exposure is greatest. Burning, itching, erythema, and swelling are the most common symptoms and can occur within minutes of sun exposure. Even brief exposure to the sun may result in intense skin pain lasting for hours, which has been described like “having a lighted match held against the skin or hot needles stuck into it” (108). Edema of the skin may be diffuse and resemble angioneurotic edema. Burning, itching, and intense pain can occur without obvious skin damage. Vesicles and bullae are absent or sparse. Epidermal intracellular vacuoles and interstitial edema are seen in fresh lesions, accompanied by acute inflammatory changes and extravasated red cells (57). Some residual scarring from vesicles or severe swelling may occur, but this is rarely severe or deforming. Pigment changes, friability, and hirsutism also are not characteristic of EPP. Thus, the cutaneous features of this disease are distinct from those of other cutaneous porphyrias. Also, in contrast to CEP, there is no discoloration or fluorescence of the teeth. It is also notable that neuropathic manifestations are not found in EPP, except rarely with advanced liver failure. Although this is an erythropoietic porphyria, the hepatic complications that develop in a small percentage of patients (probably less than 5%) are most life threatening. Liver function is usually normal in this disease, but up to 20% of patients may have minor abnormalities of liver function. In XLP, about 17% of patients had overt liver disease, suggesting that the risk of liver disease may be higher with XLP than classic EPP (145). Rapidly progressive liver disease appears to be related to the cholestatic effects of protoporphyrin and is associated with increasing protoporphyrin levels due to impaired hepatobiliary excretion and increased photosensitivity (144). Splenic enlargement and hemolysis may be accompanying features. Upper abdominal pain may suggest biliary obstruction (57). Concurrent factors impairing liver function or the metabolism of protoporphyrin to heme, such as viral hepatitis, alcohol, iron deficiency, and fasting or oral contraceptive steroids, have played a role in some patients. An enterohepatic circulation of protoporphyrin may favor its retention in the liver, especially when liver function is impaired. Liver biopsies of EPP patients with severe liver disease contain dark brown pigment with a typical birefringence under polarized light. This pigment is protoporphyrin, which has been deposited in hepatocytes, macrophages, bile canaliculi, and small bile ducts. For a detailed discussion of the hepatic complications of EPP, see Cox (144) and Thunell and coworkers (162). 99.4.8.6 Clinical and Laboratory Evaluation.  EPP should be suspected in individuals with intense skin pain after short exposure to the sun without blistering skin lesions (144). A lack of severe cutaneous signs distinguishes this disease from all other cutaneous porphyrias. Protoporphyrin concentrations are increased in the bone marrow, circulating erythrocytes, plasma, bile, and feces of EPP patients.

CHAPTER 99  Inherited Porphyrias A substantial increase in erythrocyte protoporphyrin concentration, which is a readily obtained measurement, is essential for diagnosis of EPP. Erythrocytes also exhibit red fluorescence when studied by fluorescence microscopy at 620 nm (163). However, an increased erythrocyte protoporphyrin concentration is not specific to EPP. Erythrocyte protoporphyrin concentrations are increased in other conditions such as lead poisoning, iron deficiency, anemia of chronic disease, and various hemolytic disorders, and also in all homozygous forms of porphyria and sometimes in acute porphyrias. However, the increased protoporphyrin in conditions other than EPP is in the form of zinc protoporphyrin, whereas in EPP it is free protoporphyrin (not complexed with zinc). Many assays for erythrocyte protoporphyrin or “free erythrocyte protoporphyrin” measure both the zinc-chelated and the free protoporphyrin. Free protoporphyrin is distinguished from zinc protoporphyrin by ethanol extraction or HPLC (144). In XLP, both free and zinc protoporphyrins are increased in equal proportions. Plasma porphyrins may be less increased in EPP than in other porphyrias with cutaneous manifestations (1). Other heme pathway intermediates do not accumulate in EPP. Thus, urinary porphyrin and porphyrin precursor concentrations are generally normal. Fecal total porphyrins may be normal or somewhat elevated. Lifethreatening hepatic complications of EPP are commonly preceded by increased photosensitivity and by increasing erythrocyte and plasma protoporphyrin levels. The ratio of erythrocyte to fecal protoporphyrin and the ratio of biliary protoporphyrin to biliary bile acids may also be observed to increase as liver failure develops. Ferrochelatase is a mitochondrial enzyme and can be measured in lymphocytes isolated from peripheral blood. As mentioned previously, EPP patients may have only around 20% to 30% of normal activity. Mutation analysis can be used to identify mutations and polymorphisms in the ferrochelatase gene. A high prevalence of Vitamin D deficiency has been observed in EPP patients (164) and measurement of Vitamin D 25 OH levels would be recommended for monitoring these patients. 99.4.8.7 Treatment.  Photosensitivity is managed by avoiding excessive sunlight and long-wave UV light. b-carotene was developed as a drug for treating EPP (162) and may improve tolerance to sunlight. Doses of 120 to 180 mg daily in adults are usually required to maintain serum carotene levels in the recommended range of 600–800 mg/dL. Improvement is noted 1–3 months after the initiation of treatment. With pure preparations of b-carotene, no side effects other than a mild and dose-related skin discoloration due to carotenemia have been noted. The mechanism of action may involve quenching of singlet oxygen or free radicals. The drug appears less effective in other forms of porphyria associated with photosensitivity, such as CEP and PCT. Dihydroxyacetone and lawsone (naphthoquinone),

25

which darken the skin when applied topically, partially block exposure of the dermis to light and are of some benefit in EPP. Cholestyramine, which may interrupt the enterohepatic circulation of protoporphyrin and promote its fecal excretion, has been reported to reduce liver protoporphyrin and improve cutaneous symptoms in some EPP patients. Increasing skin pigmentation by exposure to short-wave UV light may also offer some protection. Caloric restriction, drugs and hormone preparations that exacerbate acute porphyrias are often avoided in EPP, and iron deficiency should be corrected if present. Vitamin D should be supplemented if deficient. Treatment of hepatic complications is difficult and must be individualized. Cholestyramine and other porphyrin absorbents, such as activated charcoal, should be considered. Oral bile acid supplementation has shown benefit in some animal models but has been little studied in EPP patients. Resolution of hepatic complications may also occur spontaneously, especially if another reversible cause of liver dysfunction, such as viral hepatitis or alcohol, is contributing. Splenectomy may be beneficial when EPP is complicated by hemolysis and splenomegaly. Other therapeutic options include transfusions and intravenous hemin to suppress erythroid and hepatic protoporphyrin production, as well as liver transplantation. However, liver disease may recur after transplantation (165).

99.4.9 Dual Porphyrias Patients with deficiencies of more than one heme biosynthetic enzyme are classified as having dual porphyria. For example, kindreds with individuals having both VP and familial PCT have been described. Patients with deficiencies of both HMB-synthase and URO-decarboxylase may develop symptoms of AIP, PCT, or both. COPROoxidase deficiency inherited from one parent and UROsynthase deficiency from both parents was found to cause severe porphyria in an infant. Coexistence of URO-­ synthase and URO-decarboxylase deficiencies has been described in a patient with features of an erythropoietic porphyria (166). Mutation analysis was not performed on these patients to confirm that the patient actually has mutations in two different genes. This is important, as shown by studies of a patient initially thought to have both VP and AIP but who was found to have a PROTOoxidase mutation but no HMB-synthase mutation (167). A patient with both sporadic PCT and HCP due to an inherited COPRO-oxidase mutation was identified based on the urinary porphyrin pattern (168). Recently, ALAdehydratase and COPRO-oxidase gene mutations were confirmed in one patient (169), and HMB-synthase and URO-decarboxylase gene mutations in another (170), as predicted by biochemical findings. These are the first two cases of dual porphyria where mutations in two different genes have been identified.

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CHAPTER 99  Inherited Porphyrias

ACKNOWLEDGMENTS This was supported in part by grants from the National Institutes of Health (NIH) including research grants (5 R21 DK073093 and 5 R01 DK026824), a grant (1 U54 DK083909) for the Porphyrias Consortium of the NIH Rare Diseases Clinical Research Network (RDCRN), that includes funding and/or programmatic support from the NIH Office of Rare Disease Research (ORDR), and a General Clinical Research Center grant (MO1-RR000073) and a Clinical and Translational Science Award (UL1 RR029876-01), both from the National Center for Research Resources, and by a grant from the US Food and Drug Administration Office of Orphan Product Development (R01FD002604).

CHAPTERS TO CROSS-REFERENCE 2. Medicine in a Genetic Context; 3. Nature and Frequency of Genetic Disease; 7. Mutations in Human Disease: Nature and Consequences; 8. Mendelian Inhertiance; 14. Pathogenetics of Disease; 23. Diagnostic Molecular Genetics; 24. Heterozygote Testing and Carrier Screening; 29. Gene Therapy.

FURTHER READING 1. Anderson, K. E.; Sassa, S.; Bishop, D. F.; Desnick, R. J. Disorders of Heme Biosynthesis: X-Linked Sideroblastic Anemias and the Porphyrias. In The Metabolic and Molecular Basis of Inherited Disease, 8th ed.; Scriver, C. R.; Beaudet, A. L.; Sly, W. S.; Valle, D., Eds.; McGraw-Hill: New York, 2001; pp 2991–3062. 2. Anderson, K. E.; Bloomer, J. E.; Bonkovsky, H. L.; Kushner, J.; Pierach, C.; Pimstone, N.; Desnick, R. J. Recommendations for the Diagnosis and Treatment of the Acute Porphyrias. Ann. Intern. Med. 2005, 142, 439–450. 3. Badminton, M. N.; Elder, G. H. Molecular Mechanisms of Dominant Expression in Porphyria. J. Inherit. Metab. Dis. 2005, 28, 277–286. 4. Kauppinen, R. Porphyrias. Lancet 2005, 365, 241–252. 5. Schmid, R. The Porphyrias. Semin. Liver. Dis. 1998, 18, 1–101. 6. Stenson, P. D.; Ball, E. V.; Mort, M.; Phillips, A. D.; Shiel, J. A.; Thomas, N. S.; Abeysinghe, S.; Krawczak, M.; Cooper, D. N. Human Gene Mutation Database (HGMD): 2003 Update. Hum. Mutat. 2003, 21, 577–581. 7. May, B. K.; Dogra, S. C.; Sadlon, T. J.; Bhasker, C. R.; Cox, T. C.; Bottomley, S. S. Molecular Regulation of Heme Biosynthesis in Higher Vertebrates. Prog. Nucleic. Acid. Res. Mol. Biol. 1995, 51, 1–51. 8. Cotter, P. D.; Rucknagel, D. L.; Bishop, D. F. X-Linked Sideroblastic Anemia: Identification of the Mutation in the Erythroid-Specific d-Aminolevulinate Synthase Gene (ALAS2) in the Original Family Described by Cooley. Blood 1994, 84, 3915–3924. 9. Bekri, S.; May, A.; Cotter, P. D.; Al-Sabah, A. I.; Guo, X.; Masters, G. S.; Bishop, D. F. A Promoter Mutation in the ErythroidSpecific 5-Aminolevulinate Synthase (ALAS2) Gene Causes X-linked Sideroblastic Anemia. Blood 2003, 102, 698–704. 10. Shoolingin-Jordan, P. M.; Al-Daihan, S.; Alexeev, D.; Baxter, R. L.; Bottomley, S. S.; Kahari, I. D.; Roy, I.; Sarwar, M.; Sawyer, L.; Wang, S. F. 5-Aminolevulinic Acid Synthase:

Mechanism, Mutations and Medicine. Biochim. Biophys. Acta. 2003, 1647, 361. 11. Kaya, A. H.; Plewinska, M.; Wong, D. M.; Desnick, R. J.; Wetmur, J. G. Human d-Aminolevulinate Dehydratase (ALAD) Gene: Structure and Alternative Splicing of the Erythroid and Housekeeping mRNAs. Genomics 1994, 19, 242–248. 12. Doss, M. O.; Stauch, T.; Gross, U.; Renz, M.; Akagi, R.; DossFrank, M.; Seelig, H. P.; Sassa, S. The Third Case of Doss Porphyria (Delta-Amino Levulinic Acid Dehydratase Deficiency) in Germany. J. Inherit. Metab. Dis. 2004, 27, 529–536. 13. Sassa, S. ALAD Porphyria. Semin. Liver. Dis. 1998, 18, 95–101. 14. Akagi, R.; Kato, N.; Inoue, R.; Anderson, K. E.; Jaffe, E. K.; Sassa, S. Delta-Aminolevulinate Dehydratase (ALAD) Porphyria: The First Case in North America with Two Novel ALAD Mutations. Mol. Genet. Metab. 2006, 87, 329–336. 15. Schwartz, B. S.; Lee, B. K.; Sewart, W.; Ahn, K. D.; Springer, K.; Kelsey, K. Associations of Delta-Aminolevulinic Acid Dehydratase Genotype with Plant, Exposure Duration, and Blood Lead and Zinc Protopophyrin Levels in Korean Lead Workers. Am. J. Epidemol. 1995, 142, 738–745. 16. Alexander, B. H.; Checkoway, H.; Costa-Mallen, P.; Faustman, E. M.; Woods, J. S.; Kelsey, K. T.; van Netten, C.; Costa, L. G. Interaction of Blood Lead and Delta-Aminolevulinic Acid Dehydratase Genotype on Markers of Heme Synthesis and Sperm Production in Lead Smelter Workers. Environ. Health. Perspect. 1998, 106, 213–216. 17. Fleming, D. E.; Chettle, D. R.; Wetmur, J. G.; Desnick, R. J.; Robin, J. P.; Boulay, D.; Richard, N. S.; Gordon, C. L.; Webber, C. E. Effect of the Delta-Aminolevulinate Dehydratase Polymorphism on the Accumulation of Lead in Bone and Blood in Lead Smelter Workers. Environ. Res. 1998, 77, 49–61. 18. Hu, H.; Wu, M. T.; Cheng, Y.; Sparrow, D.; Weiss, S.; Kelsey, K. The Delta-Aminolevulinic Acid Dehydratase (ALAD) Polymorphism and Bone and Blood Lead Levels in CommunityExposed Men: The Normative Aging Study. Environ. Health. Perspect. 2001, 109, 827–832. 19. Sithisarankul, P.; Schwartz, B. S.; Lee, B. K.; Kelsey, K. T.; Strickland, P. T. Aminolevulinic Acid Dehydratase Genotype Mediates Plasma Levels of the Neurotoxin, 5-Aminolevulinic Acid, in Lead-Exposed Workers. Am. J. Ind. Med. 1997, 32, 15–20. 20. Wetmur, J. G. Influence of the Common Human d-Aminolevulinate Dehydratase Polymorphism on Lead Body Burden. Environ. Health. Perspect. 1994, 102 (Suppl. 3), 215–219. 21. Anderson, P. M.; Reddy, R. M.; Anderson, K. E.; Desnick, R. J. Characterization of the PBG-Deaminase Deficiency in Acute Intermittent Porphyria. I. Immunologic Evidence for Heterogeneity of the Genetic Defect. J. Clin. Invest. 1981, 68, 1–12. 22. Shoolingin-Jordan, P. M.; Al-Dbass, A.; McNeill, L. A.; Sarwar, M.; Butler, D. Human Porphobilinogen Deaminase Mutations in the Investigation of the Mechanism of Dipyrromethane Cofactor Assembly and Tetrapyrrole Formation. Biochem. Soc. Trans. 2003, 31, 731–735. 23. Grandchamp, B. Acute Intermittent Porphyria. Semin. Liver. Dis. 1998, 18, 17–24. 24. Brownlie, P. D.; Lambert, R.; Louie, G. V.; Jordan, P. M.; Blundell, T. L.; Warren, M. J.; Cooper, J. B.; Wood, S. P. The Three-Dimensional Structures of Mutants of Porphobilinogen Deaminase: Toward an Understanding of the Structural Basis of Acute Intermittent Porphyria. Protein. Sci. 1994, 3, 1644–1650. 25. Wood, S.; Lambert, R.; Jordan, M. Molecular Basis of Acute Intermittent Porphyria. Mol. Med. Today 1995, 5, 232–239. 26. Aizencang, G.; Solis, C.; Bishop, D. F.; Warner, C.; Desnick, R. J. Human Uroporphyrinogen-III Synthase: Genomic Organization, Alternative Promoters, and Erythroid-Specific Expression. Genomics 2000, 70, 223–231. 27. Mathews, M. A.; Schubert, H. L.; Whitby, F. G.; Alexander, K. J.; Schadick, K.; Bergonia, H. A.; Phillips, J. D.; Hill, C. P.

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CHAPTER 99  Inherited Porphyrias 156. Ohgari, Y.; Sawamoto, M.; Yamamoto, M.; Kohno, H.; Taketani, S. Ferrochelatase Consisting of Wild-Type and Mutated Subunits from Patients with a Dominant-Inherited Disease, Erythropoietic Protoporphyria, Is an Active but Unstable Dimer. Hum. Mol. Genet. 2005, 14, 327–334. 157. Abitbol, M.; Bernex, F.; Puy, H.; Jouault, H.; Deybach, J. C.; Guénet, J. L.; Montagutelli, X. A Mouse Model Provides Evidence that Genetic Background Modulates Anemia and Liver Injury in Erythropoietic Protoporphyria. Am. J. Physiol. Gastrointest. Liver. Physiol. 2005, 288, G1208–G1216. 158. Libbrecht, L.; Meerman, L.; Kuipers, F.; Roskams, T.; Desmet, V.; Jansen, P. Liver Pathology and Hepatocarcinogenesis in a Long-Term Mouse Model of Erythropoietic Protoporphyria. J. Pathol. 2003, 199, 191–200. 159. Han, A. P.; Fleming, M. D.; Chen, J. J. Heme-Regulated eIF2alpha Kinase Modifies the Phenotypic Severity of Murine Models of Erythropoietic Protoporphyria and Beta-thalassemia. J. Clin. Invest. 2005, 115, 1562–1570. 160. Fontanellas, A.; Mazurier, F.; Landry, M.; Taine, L.; Morel, C.; Larou, M.; Daniel, J. Y.; Montagutelli, X.; de Salamanca, R. E.; de Verneuil, H. Reversion of Hepatobiliary Alterations by Bone Marrow Transplantation in a Murine Model of Erythropoietic Protoporphyria. Hepatology 2000, 32, 73–81. 161. Pawliuk, R.; Tighe, R.; Wise, R. J.; Mathews-Roth, M. M.; Leboulch, P. Prevention of Murine Erythropoietic Protoporphyria-Associated Skin Photosensitivity and Liver Disease by Dermal and Hepatic Ferrochelatase. J. Invest. Dermatol. 2005, 124, 256–262. 162. Thunell, S.; Harper, P.; Brun, A. Porphyrins, Porphyrin Metabolism and Porphyrias. IV. Pathophysiology of Erythyropoietic Protoporphyria—Diagnosis, Care and Monitoring of the Patient. Scand. J. Clin. Lab. Invest. 2000, 60, 581–604. 163. Murphy, G. M. Diagnosis and Management of the Erythropoietic Porphyrias. Dermatol. Ther. 2003, 16, 57–64.

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164. Spelt, J. M.; de Rooij, F. W.; Wilson, J. H.; Zandbergen, A. A. Vitamin D Deficiency in Patients with Erythropoietic Protoporphyria. J. Inherit. Metab. Dis. 2009, [Epub] Jan 10. 165. McGuire, B. M.; Bonkovsky, H. L.; Carithers, R. L., Jr.; Chung, R. T.; Goldstein, L. I.; Lake, J. R.; Lok, A. S.; Potter, C. J.; Rand, E.; Voigt, M. D., et al. Liver Transplantation for Erythropoietic Protoporphyria Liver Disease. Liver. Transpl. 2005, 11, 1590–1596. 166. Freesemann, A. G.; Hofweber, K.; Doss, M. O. Coexistence of Deficiencies of Uroporphyrinogen III Synthase and Decarboxylase in a Patient with Congenital Erythropoietic Porphyria and in his Family. Eur. J. Clin. Chem. Clin. Biochem. 1997, 35, 35–39. 167. Weinlich, G.; Doss, M. O.; Sepp, N.; Fritsch, P. Variegate Porphyria with Coexistent Decrease in Porphobilinogen Deaminase Activity. Acta. Derm. Venereol. 2001, 81, 356–359. 168. Doss, M. O.; Gross, U.; Puy, H.; Doss, M.; Kühnel, A.; Jacob, K.; Deybach, J. C.; Nordmann, Y. Coexistence of Hereditary Coproporphyria and Porphyria Cutanea Tarda: A New Form of Dual Porphyria. Med. Klin. (Munich). 2002, 97, 1–5, (German). 169. Akagi, R.; Inoue, R.; Muranaka, S.; Tahara, T.; Taketani, S.; Anderson, K. E.; Phillips, J. D.; Sassa, S. Dual Gene Defects Involving Delta-Aminolaevulinate Dehydratase and Coproporphyrinogen Oxidase in a Porphyria Patient. Br. J. Haematol. 2006, 132, 237–243. 170. Harraway, J. R.; Florkowski, C. M.; Sies, C.; George, P. M. Dual Porphyria with Mutations in Both the UROD and HMBS Genes. Ann. Clin. Biochem. 2006, 43, 80–82.

RELEVANT WEB PAGES Porphy www.porphyriafoundation.com Pore www.porphyria-europe.org

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CHAPTER 99  Inherited Porphyrias Biographies Robert J Desnick, MD, PhD, is Dean for Genetics and Genomics and Professor and Chairman of the Department of Genetics and Genomic Sciences at The Mount Sinai School of Medicine and Physician-in-Chief of the Department of Medical Genetics and Genomics at the Mount Sinai Hospital in New York City. He is board-certified in Clinical, Biochemical, and Molecular Genetics by the American Board of Medical Genetics and is a Fellow of the American Academy of Pediatrics. He has published over 600 research articles and chapters, including nine edited books. He is a founder and Past-President of the Association of Professors of Human and Medical Genetics and is a past Chair of the Association of American Medical Colleges (AAMC). He is an elected member of the American Pediatric Society, American Society for Clinical ­Investigation, American Association of Physicians, American Academy for the Advancement of Science (Fellow), and the Institute of Medicine of the National Academy of Sciences. Manisha Balwani, MD, MS, received her MD degree from the University of Bombay and a Master’s degree in Genetics at the University of Pittsburgh. She is trained in Internal Medicine as well as Clinical and Biochemical Genetics and is an Assistant Professor in the Department of Genetics and Genomic Sciences at the Mount Sinai School of Medicine. Dr Balwani is the ­Co-Director of the Comprehensive Porphyria Diagnostic and Treatment Center at Mount Sinai, which has been designated as one of the five “Centers of Excellence” by the ­American ­Porphyria Foundation. She is part of the American Porphyria Foundation’s “Protect the Future” program. She is currently involved in research in the field of Porphyria as well as in clinical ­trials for development for newer therapies.

Karl E Anderson, MD, is Professor of Preventive Medicine and Community Health, Internal Medicine and Pharmacology and Toxicology at the University of Texas Medical Branch in Galveston, Texas. He is board-certified in Internal Medicine and Gastroenterology and a ­Fellow of the American College of Physicians. He has published over 200 articles, book ­chapter and reviews. He is Past-President of the Association for Patient-Oriented Research and an elected member of the American Gastroenterological Association, the American Association for the Study of Liver Diseases, the American Federation for Medical Research, the Southern ­Society for Clinical Investigation, and the American Association for the Advancement of Science.