Clinical Genetic Testing In Psychiatry: Prospects And Challenges

Clinical Genetic Testing In Psychiatry: Prospects And Challenges

S364 Abstracts of the XXIV World Congress of Psychiatric Genetics (WCPG) 2016 Concurrent Symposia Session 3 CLINICAL GENETIC TESTING IN PSYCHIATRY: ...

42KB Sizes 2 Downloads 46 Views

S364

Abstracts of the XXIV World Congress of Psychiatric Genetics (WCPG) 2016

Concurrent Symposia Session 3 CLINICAL GENETIC TESTING IN PSYCHIATRY: PROSPECTS AND CHALLENGES

Bernard Lerer (Chair)1, Anthony C. Altar (Co-chair)2, Francis McMahon (Discussant)3 1

Biological Psychiatry Laboratory, Hadassah - Hebrew University Medical Center, Jerusalem, Israel 2 Assurex Health, Inc 3 NIH/NIMH Overall Abstract Diagnostic tests are an important tool in medical practice. Ideally, they provide the clinician with valid and accurate information as to whether a disease is present or absent in a particular patient or whether the patient can be expected to respond or not respond to a particular treatment or manifest adverse effects as a consequence thereof. Biomarkers of various types, including genetic biomarkers, can serve as diagnostic tests. Genetic markers that can be used to predict response to medication or adverse effects are a central research objective of pharmacogenomics. A pivotal requirement of diagnostic tests is that they be accurate and sensitive. A further characteristic that ensures generalizability is that the test be valid for different populations. Large scale clinical research is needed to fulfill such requirements. In the area of diagnostic testing, including genetic tests, regulatory requirements are considerably less stringent than in the licensing of pharmaceutical agents. This panel will focus on clinical genetic testing in psychiatry with an emphasis on pharmacogenomic tests that are used to predict response to and adverse effects of psychiatric drugs. Several such tests are currently being marketed in various countries and others are in development in commercial and academic research settings. This panel will present four such initiatives with an emphasis on empirical data regarding the validity of these tests and justification for their use. Anthony C. Altar will present data on GeneSight Psychotropic, a test that is based on a composite phenotype derived from allelic variations in six genes that encode cytochrome P450 (CYP) enzymes, two genes that encode UGT enzymes, and four pharmacodynamic genes. Miquel Tuson will present data on Neuropharmagen, a test that integrates pharmacogenomic data from the analysis of several pharmacokinetic and pharmacodynamic genes with drug-drug interactions to provide recommendations for psychoactive drug treatment, including a randomized clinical trial conducted in patients with major depressive disorder. Dekel Taliaz will describe the development of prediction algorithms for the efficacy and adverse effects of current antidepressants, with up to 77% accuracy (76% specificity and 79% sensitivity) based on the application of machine learning algorithms to genetic data combined with clinical and demographic information in large databases. Bernard Lerer will describe a series of experiments in which association of two single nucleotide polymorphisms with susceptibility to antipsychotic-induced parkinsonism was identified in clinical studies, validated and then tested in a large

replication study. He will consider the difficulty in establishing the clinical utility of common genetic biomarkers even with a carefully recruited, well-powered sample. Francis McMahon will serve as Discussant of these presentations. The aim of this panel is to facilitate a discussion of genetic testing in clinical psychiatry that is based on data generated regarding tests currently in use or in development and, on this background, to consider the significant challenges that need to be addressed in the course of developing such instruments.

Disclosure Taliaz Diagnostics - Consultant, Self http://dx.doi.org/10.1016/j.euroneuro.2016.09.387

PHARMACOGENOMIC INFORMATION IN THE TREATMENT OF MAJOR DEPRESSION: RESULTS FROM A RANDOMIZED CLINICAL TRIAL

Miquel Tuson1, Víctor Pérez2, Ariana Salavert1, Jordi Espadaler1, Jerónimo Saiz3, Julio Bobes4, Eduard Vieta5, Enric Àlvarez6, José M. Menchón7 1

AB-Biotics Institut de Neuropsiquiatria i Addiccions (INAD), Hospital del Mar, Universitat Autònoma de Barcelona, and CIBERSAM (Barcelona, Spain) 3 Departamento de Psiquiatría, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Hospital Universitario Ramón y Cajal, Universidad de Alcalá, and CIBERSAM (Madrid, Spain) 4 Área de Psiquiatría, Facultad de Medicina, Universidad de Oviedo. Instituto Universitario de Neurociencias del Principado de Asturias (INEUROPA), and CIBERSAM (Oviedo, Spain) 5 Institut Clínic de Neurociències, Hospital Clínic de Barcelona, Universitat de Barcelona. Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), and CIBERSAM (Barcelona, Spain) 6 Servei de Psiquiatria, Hospital de la Santa Creu i Sant Pau. Institut d'Investigació Biomèdica Sant Pau, Universitat Autònoma de Barcelona, and CIBERSAM (Barcelona, Spain) 7 Departament de Psiquiatria, Hospital Universitari de Bellvitge, Institut d’Investigació Biomèdica de Bellvitge (IDIBELL). Departament de Ciències Clíniques, Facultat de Medicina, Universitat de Barcelona, and CIBERSAM (Barcelona, Spain) 2

Abstract Mental disorders are one of the leading causes of disability globally. Inherited genetic variation in pharmacokinetic (PK) and pharmacodynamic (PD) genes may contribute to the observed