Risk Factors for Abdominal Aortic Aneurysm in the Korean Population

Risk Factors for Abdominal Aortic Aneurysm in the Korean Population

Accepted Manuscript Risk factors for abdominal aortic aneurysm in the Korean population Sang-Ah Han, M.D., Ph.D., Jin Hyun Joh, M.D., Ph.D., Ho-Chul P...

484KB Sizes 0 Downloads 49 Views

Accepted Manuscript Risk factors for abdominal aortic aneurysm in the Korean population Sang-Ah Han, M.D., Ph.D., Jin Hyun Joh, M.D., Ph.D., Ho-Chul Park, M.D., Ph.D. PII:

S0890-5096(17)30250-9

DOI:

10.1016/j.avsg.2016.08.044

Reference:

AVSG 3132

To appear in:

Annals of Vascular Surgery

Received Date: 2 March 2016 Revised Date:

4 August 2016

Accepted Date: 13 August 2016

Please cite this article as: Han SA, Joh JH, Park HC, Risk factors for abdominal aortic aneurysm in the Korean population, Annals of Vascular Surgery (2017), doi: 10.1016/j.avsg.2016.08.044. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

ACCEPTED MANUSCRIPT 1

Title: Risk factors for abdominal aortic aneurysm in the Korean population

2 3

5

RI PT

4

Authors : Sang-Ah Han, M.D., Ph.D., Jin Hyun Joh, M.D., Ph.D., Ho-Chul Park, M.D., Ph.D.

SC

6

M AN U

7 8 9 10

Institution : Department of Surgery, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea,

TE D

11 12

AC C

14

EP

13

15

Corresponding author : Jin Hyun Joh

16

(05278) 892 Dongnam-ro, Gangdong-gu, Seoul, Korea

17

Tel : +82-2-440-6261, Fax : +82-2-440-6296,

18

Email : [email protected]

19 1

ACCEPTED MANUSCRIPT Abstract

21

Background: Ultrasound screening shows a clinical benefit in reducing abdominal aortic aneurysm

22

(AAA)-related mortality. However, its cost-effectiveness remains unclear. Understanding the

23

relationship between risk factors and AAA is important to maximize the benefit of AAA screening.

24

However, risk factors for AAA have not been reported in Korea. The purpose of this study was to

25

determine the prevalence of and risk factors for AAA among the Korean population.

26

Methods: The study population consisted of patients >50 years of age who consented for AAA

27

screening. Screening was performed as follows for all participants: collection of demographic

28

information, including risk factors, physical examination, and ultrasound screening. We measured the

29

maximal diameter of the aorta from the outer to outer layer at five levels: suprarenal, renal, and

30

infrarenal aorta, and bilateral common iliac arteries. AAA was defined as maximal aortic diameter >3

31

cm. The risk factors and risk ratio for AAA were determined. Chi-square test and a logistic regression

32

model were used for statistical analysis. All P-values <0.05 were considered significant.

33

Results: A total of 2,035 participants were enrolled. Among them, 908 (44.6%) were men and 1,127

34

(55.4%) were women. Mean age was 66.9 ± 10.3 years (range, 23–95 years). AAA was detected in 18

35

of 908 (2.0%) males and 4 of 1,127 (0.4%) females. The presence of an AAA was significantly

36

correlated with male sex (P <0.001), advanced age (P = 0.01), smoking (P <0.001), alcohol

37

consumption (P <0.01), and the presence of pulmonary disease (P = 0.01). Multivariate analysis

38

revealed that smoking was the only significant risk factor for AAA.

39

Conclusion: The prevalence of AAA was 2.0% in males and 0.4% in females. Male sex, old age,

40

smoking, alcohol use, and pulmonary disease are possible risk factors for AAA in the general Korean

41

population. Smoking is the strongest risk factor for the development of AAA.

AC C

EP

TE D

M AN U

SC

RI PT

20

42

2

ACCEPTED MANUSCRIPT 43

Introduction An abdominal aortic aneurysm (AAA) can remain asymptomatic or produce minimal symptoms for

45

many years, despite a large diameter. However, AAA rupture is associated with abdominal distension,

46

a pulsating abdominal mass, hypovolemic shock, and eventual death, if not repaired immediately.

47

Growing evidence suggests that ultrasound screening can be effective in avoiding the need for

48

emergent operations and reducing AAA-related mortality.1-3

RI PT

44

Despite this evidence of a clinical benefit, the cost-effectiveness of ultrasound screening remains

50

unclear.4,5 Estimates of cost-effectiveness for ultrasound screening of AAA are country-specific

51

because of variable prevalence of AAA and ultrasound costs. An international consensus suggests that

52

one-off ultrasound screening in men aged about 65 years is cost-effective.4

M AN U

SC

49

The relationship between risk factors and AAA is important to maximize the benefit of AAA

54

screening. Classic risk factors for atherosclerosis are the same as those for AAA, such as cigarette

55

smoking, male sex, age, hypertension, and hyperlipidemia.3,6 However, the risk factors for AAA have

56

not been reported in Korea. The purpose of this study was to determine the prevalence and risk factors

57

for AAA in the Korean population.

TE D

53

Material and Methods

AC C

59

EP

58

60

The study population was recruited from Hanam City, Seoul City, Ulsan City, and Uiwang City,

61

South Korea and was one extended from our previous study.7 Recruitment was achieved with an

62

official document of authority without any advertisement or reward. Subjects >50 years of age who

63

consented to AAA screening were included in the study. Subjects of any age who had a family history

64

of AAA were likewise included. We excluded subjects diagnosed with an AAA, those with a history

65

of open or endovascular AAA repair, history of abdominal aortic surgery such as aortobifemoral 3

ACCEPTED MANUSCRIPT 66

bypass, life expectancy <2 years based on the Statistics Korea life table, and those who refused AAA

67

screening. This study was approved by the Institutional Review Board (IRB) of Kyung Hee

68

University Hospital at Gangdong. Screening was performed using the same strategy as described in our previous study. Briefly, history

70

was taken from each participant and all participants underwent physical and ultrasound examinations.

71

We obtained the demographic information with a detailed questionnaire. We investigated the patients

72

for history of diabetes, hypertension, hyperlipidemia, heart disease, pulmonary disease,

73

cerebrovascular disease, and renal function impairment, and inquired about their surgical history.

74

Questions about the family history of AAA, stroke, and peripheral arterial occlusive disease were also

75

asked. Social history included smoking history, alcohol history, and amount of exercise. All

76

participants were asked whether they had any aneurysm-related symptoms, such as abdominal pain or

77

back pain. After obtaining the pertinent history, the subject’s abdomen was palpated to evaluate the

78

presence of a pulsating mass. Finally, duplex scanning was performed after fasting for 8 hours.

79

Duplex scanning was performed by experienced sonographers who were certified Registered Vascular

80

Technologists by the American Registry for Diagnostic Medical Sonography. We used two types of

81

ultrasound machines, namely Zonare (Zonare Medical Systems, Mountain View, CA, USA) and HD7

82

(Philips, Amsterdam, the Netherlands). A 2.5–5 MHz convex ultrasound probe was used for the

83

examination. Duplex scanning was done from the infradiaphragmatic level to bilateral iliac arteries.

84

We measured the maximal diameter of the aorta from the outer to outer layer. Anteroposterior and

85

lateral diameters were measured. We recorded the two diameters at the levels of the suprarenal, renal,

86

and infrarenal aorta, and the right and left iliac arteries. The “suprarenal” diameter was measured at

87

the level between the superior mesenteric artery and the renal artery. The “renal” diameter was the

88

aortic diameter at the level of the renal artery. If both renal arteries were projected at the same level,

89

the maximal diameter at the level of the renal artery was measured in the anteroposterior plane. The

90

“infrarenal” diameter was measured at the level between the lower renal artery and the aortic

AC C

EP

TE D

M AN U

SC

RI PT

69

4

ACCEPTED MANUSCRIPT bifurcation. The iliac artery diameters were measured at the common iliac artery between the aortic

92

bifurcation and the origin of the internal iliac artery on both sides. If the iliac artery was tortuous, the

93

diameter of the iliac artery was measured only in the anteroposterior plane. If bowel gas interfered

94

with adequate measurement of the diameter, subjects were asked to return for re-examination the next

95

day.

RI PT

91

AAA was defined as maximal aortic diameter >3 cm. Maximal aortic diameter was calculated as the

97

sum of the diameter on the anteroposterior plane and the lateral plane, divided by 2. Hypertension and

98

hyperlipidemia were defined as intake of antihypertensive and lipid-lowering medications,

99

respectively. Cardiovascular risk factors included arrhythmia, coronary artery disease, myocardial

100

infarction, angina, and a history of coronary angioplasty or stenting. Cerebrovascular risk factors

101

included transient ischemic attack, reversible ischemic neurologic deficit, and stroke. Respiratory risk

102

factors included chronic obstructive pulmonary disease, asthma, pneumonia, and pulmonary

103

tuberculosis. Renal impairment was defined as undergoing dialysis.

M AN U

SC

96

We used SPSS ver. 19.0 software (SPSS, Inc., Chicago, IL, USA) for the statistical analysis. The

105

risk factors and risk ratio for AAA were determined. Chi-square test was used for the univariate

106

analysis, and a logistic regression model was used for the multivariate analysis. All P-values <0.05

107

were considered significant.

EP

TE D

104

AC C

108 109

Results

110

A total of 2,035 participants were enrolled. All participants completed the questionnaires and

111

underwent the examinations. Among them, 908 (44.6%) were men and 1,127 (55.4%) were women.

112

Mean age was 66.9 ± 10.3 years (range, 23–95 years). An AAA was detected in 22 (1.1%) individuals

113

(Table I). The prevalence of AAA was 18 of 908 (2.0%) males, and 4 of 1,127 (0.4%) females, and

5

ACCEPTED MANUSCRIPT prevalence was found to increase with age. The average diameter of the aneurysm was 49.7±18.2 mm

115

(range 30.3-80.7 mm). No participant <50 years of age had an AAA. Three (0.8%) of 382, 4 (0.6%) of

116

633, and 11 (1.5%) of 744 had an AAA at 50–59 years, 60–69 years, and 70–79 years, respectively.

117

Participants ≥80 years old had the highest prevalence, with 4 of 182 (2.2%) having the disease. A

118

high-risk group, based on the Centers for Medicare and Medicaid Services guidelines, was analyzed,

119

which included those with a family history of AAA and men 65–75 years who have smoked at least

120

100 cigarettes throughout their life. In this group, 15 (3.2%) of 476 patients had an AAA.

SC

121

RI PT

114

Risk factors are shown in Table II. Hypertension was the most common risk factor, with 998 (49.0%) subjects having hypertension and taking antihypertensive medications. This was followed by smoking

123

(n=759; 37.3%), alcohol consumption (n=749; 36.8%), hyperlipidemia (n=577; 28.4%), and diabetes

124

(n=387; 19.0%). A total of 196 (9.6%) subjects had coronary artery disease, mainly ischemic heart

125

disease. In total, 130 (6.4%) had a cerebrovascular problem, including transient ischemic attack,

126

reversible ischemic neurologic deficit, and stroke, and 52 (2.6%) had pulmonary disease, mainly

127

chronic obstructive pulmonary disease. Twenty-two (1.1%) had end-stage renal disease and were

128

undergoing hemodialysis.

TE D

M AN U

122

The univariate analysis of risk factors for AAA is shown in Table III. The presence of AAA was

130

strongly correlated with male sex (P <0.001), increased age (P = 0.01), smoking (P <0.001), alcohol

131

consumption (P <0.01), and the presence of pulmonary disease (P = 0.01). Multivariate analysis

132

revealed that smoking was the only significant factor for AAA (Table IV). The odds ratio (OR) was

133

7.4 (95% confidence interval [CI], 2.55–21.47, P <0.001). Male sex, age, alcohol, and pulmonary

134

disease were not significant in the multivariate analysis.

AC C

EP

129

135 136

Discussion

6

ACCEPTED MANUSCRIPT This study showed that the prevalence of AAA in a general Korean population aged >50 years is

138

1.1%. Males were five times more likely to have an AAA compared to females. In addition, the

139

frequency of AAA increased with age. AAA was detected in 2.2% of subjects >80 years. Smoking is

140

a well-known risk factor for AAA. In our study, smoking was the only significant risk factor for the

141

development of AAA in the multivariate analysis. Smokers are 7.4 times more likely to have an AAA

142

than nonsmokers.

RI PT

137

According to research from the United States and from European countries, AAAs occur in 5–10%

144

of men and 0.5–1.5% of women aged 65–79 years.8,9 Known risk factors include age, smoking, male

145

sex, and family history.8 AAAs are 3–5 times more likely to develop in patients with a smoking

146

history. Approximately 9,000 deaths annually are linked to AAAs in the United States, mostly in men

147

>65 years old. However, only a few studies have been performed on the incidence of AAA in the

148

Asian population, apart from reported differences in the occurrence of AAAs in black and Caucasian

149

populations. The prevalence of AAA in our study was 2.0% of males and 0.4% of females in a Korean

150

population. AAA was detected 2.1% of men aged 65-79 years. There was no AAA detected in women

151

aged 65-79 years. The prevalence of AAAs in high-risk Koreans was 3.2%. Our results showed that

152

AAA is not uncommon in the Korean population and that the incidence is comparable to that in

153

Western countries. Data from Malaysia support our results, with incidence rates for the at-risk male

154

population >50 years of 2.56%, and 7.83% for males >70 years.10

EP

TE D

M AN U

SC

143

Mortality after rupture of an AAA approaches 80% for patients who reach the hospital and 50% for

156

those who undergo emergency surgery.8 Fatal outcomes after a ruptured AAA have been highlighted

157

by AAA screening programs for decades, because mortality from an AAA decreases significantly

158

among patients in whom the AAA is discovered at screening (men 65–79 years: OR = 0.60; 95% CI,

159

0.47–0.78).9 Therefore, establishing a modernized screening program is necessary. A meta-analysis

160

that analyzed four contemporary randomized controlled trials strongly supported the benefits of

161

screening for AAAs. 3

AC C

155

7

ACCEPTED MANUSCRIPT Identifying the risk factors for AAA is important to increase the efficacy of screening programs.

163

Independent risk factors for AAA have not been clearly defined in multivariate analyses of large

164

patient populations. The classic risk factors for atherosclerosis, such as tobacco smoking, male sex,

165

age, hypertension, and hyperlipidemia, are all risk factors for AAA.3,6,11 Our data revealed that male

166

sex, age, alcohol, and pulmonary disease were significant risk factors on univariate analysis; however,

167

smoking was the only significant factor on multivariate analysis.

RI PT

162

Although, one study reported that current smoking is not a significant risk factor for AAA,12

169

smoking was the strongest risk factor in our study, which is similar to several other studies.13-18 A

170

dose-response effect of smoking duration and quantity was reported in a prospective analysis of the

171

Tromsø study.19 Smoking increases the expansion rate and rupture risk of an AAA.20,21 Inflammation,

172

proteolysis, smooth muscle cell apoptosis, and angiogenesis have been implicated in the pathogenesis

173

of AAAs.22,23 Nicotine stimulates matrix metalloproteinase expression by vascular smooth muscle,

174

endothelial, and inflammatory cells in the vascular wall and induces angiogenesis in aneurysmal

175

tissues.24-26

TE D

M AN U

SC

168

An interesting finding of our study was the correlation between alcohol consumption and the risk of

177

AAA on univariate analysis. Studies investigating the role of alcohol in the development of AAAs are

178

few. Moderate alcohol consumption is considered to decrease the risk of cardiovascular events and

179

reduce acute myocardial infarction.27 A Swedish cohort study also showed a lower risk for AAA with

180

moderate alcohol consumption, specifically wine and beer.28 Tailor et al. demonstrated a linear dose-

181

response relationship, with a relative risk of 1.57 in subjects consuming 50 g of pure alcohol per day

182

and 2.47 in hypertensive subjects consuming 100 g per day.29 Similarly, two studies focused on the

183

negative effect of alcohol consumption on the pathogenesis of AAA. Alcohol is independently

184

correlated with aortic diameter.30 Wong et al. reported that baseline alcohol consumption is

185

independently associated with a diagnosis of AAA after adjusting for other risk factors,

186

including smoking, hypertension, and body mass index, (p for trend = .03), with a maximum hazard

AC C

EP

176

8

ACCEPTED MANUSCRIPT ratio of 1.21 (95% CI, 0.78–1.87) for≥ 30.0 g daily alcohol consumption.31 According to an alcohol

188

consumption and dietary habit survey among Koreans, 2,962 of 3,597 men (82.3%) were alcohol

189

drinkers. A total of 1,002 subjects (27.9%) drank ≥30 g of alcohol per day and 248 subjects (6.8%)

190

drank ≥80 g of alcohol per day. The amount of alcohol consumed per day increased with increasing

191

age. Alcohol drinkers also tend to be smokers.32 This issue is controversial but the unique Korean

192

drinking practice could affect the prevalence of AAA.

SC

RI PT

187

Our study has several limitations. Firstly, the study population was relatively small. Therefore, some

194

of the statistical correlations were weak. Secondly, our study population was comprised of citizens

195

from specific areas and was nationwide. Therefore, the prevalence of AAA may have a small

196

selection bias. Despite these limitations, it is recommended to perform ultrasound screening of AAA

197

for male smokers ≥65 years in Korea.

199

Conclusions

TE D

198

M AN U

193

In this Korean population, the prevalence of AAA was 2.0% in males and 0.4% in females. Risk

201

factors for development of AAA included male sex, old age, smoking, alcohol use, and pulmonary

202

disease. Those patients at high risk for AAA had a higher prevalence of AAA (3.2%). Smoking is the

203

strongest risk factor for the development of AAA. A nationwide screening study is required to

204

evaluate the prevalence of AAA and its risk factors.

AC C

205

EP

200

206 207 9

ACCEPTED MANUSCRIPT 208

References

209

1.

Norman PE, Jamrozik K, Lawrence-Brown MM, et al. Population based randomised controlled trial on impact of screening on mortality from abdominal aortic aneurysm. BMJ

211

2004;329:1259.

212

2.

213 214

Lindholt JS, Juul S, Fasting H, et al. Screening for abdominal aortic aneurysms: single centre randomised controlled trial. BMJ 2005;330:750.

3.

RI PT

210

Svensjo S, Bjorck M, Wanhainen A. Editor's choice: five-year outcomes in men screened for abdominal aortic aneurysm at 65 years of age: a population-based cohort study. Eur J Vasc

216

Endovasc Surg 2014;47:37-44.

218 219

abdominal aortic aneurysm screening programme in England. Br J Surg 2014;101:976-82. 5.

220 221

Glover MJ, Kim LG, Sweeting MJ, et al. Cost-effectiveness of the National Health Service

M AN U

4.

Spronk S, van Kempen BJ, Boll AP, et al. Cost-effectiveness of screening for abdominal aortic aneurysm in the Netherlands and Norway. Br J Surg 2011;98:1546-55.

6.

Chun KC, Teng KY, Chavez LA, et al. Risk factors associated with the diagnosis of

TE D

217

SC

215

222

abdominal aortic aneurysm in patients screened at a regional Veterans Affairs health care

223

system. Ann Vasc Surg 2014;28:87-92.

225 226

Korean population. Yonsei Med J 2013;54:48-54. 8.

227

2005;142:203-11.

9.

230 231 232

Fleming C, Whitlock EP, Beil TL, et al. Screening for abdominal aortic aneurysm: a bestevidence systematic review for the U.S. Preventive Services Task Force. Ann Intern Med

228 229

Joh JH, Ahn HJ, Park HC. Reference diameters of the abdominal aorta and iliac arteries in the

EP

7.

AC C

224

Cosford PA, Leng GC. Screening for abdominal aortic aneurysm. Cochrane Database Syst Rev 2007(2):CD002945.

10.

Yii MK. Epidemiology of abdominal aortic aneurysm in an Asian population. ANZ J Surg 2003;73:393-5. 10

ACCEPTED MANUSCRIPT 233

11.

Singh K, Bonaa KH, Jacobsen BK, et al. Prevalence of and risk factors for abdominal aortic

234

aneurysms in a population-based study : The Tromso Study. Am J Epidemiol 2001;154:236-

235

44. 12.

237 238

Korean male population. Ann Vasc Surg 2015;29:215-21. 13.

239

Wilmink TB, Quick CR, Day NE. The association between cigarette smoking and abdominal aortic aneurysms. J Vasc Surg 1999;30:1099-105.

14.

Lederle FA, Johnson GR, Wilson SE, et al. Yield of repeated screening for abdominal aortic

SC

240

Cho WP, Park IS, Jeon YS, et al. Vascular disease prevalence and risk factors in a screened

RI PT

236

aneurysm after a 4-year interval. Aneurysm Detection and Management Veterans Affairs

242

Cooperative Study Investigators. Arch Intern Med 2000;160:1117-21.

243

15.

M AN U

241

Lindholt JS, Heegaard NH, Vammen S, et al. Smoking, but not lipids, lipoprotein(a) and

244

antibodies against oxidised LDL, is correlated to the expansion of abdominal aortic

245

aneurysms. Eur J Vasc Endovasc Surg 2001;21:51-6. 16.

247 248

Tornwall ME, Virtamo J, Haukka JK, et al. Life-style factors and risk for abdominal aortic aneurysm in a cohort of Finnish male smokers. Epidemiology 2001;12:94-100.

17.

TE D

246

Oh SH, Chang SA, Jang SY, et al. Routine screening for abdominal aortic aneurysm during clinical transthoracic echocardiography in a Korean population. Echocardiography

250

2010;27:1182-7. 18.

252 253

aneurysm in a cohort of more than 3 million individuals. J Vasc Surg 2010;52:539-48.

19.

254 255

Kent KC, Zwolak RM, Egorova NN, et al. Analysis of risk factors for abdominal aortic

AC C

251

EP

249

Forsdahl SH, Singh K, Solberg S, et al. Risk Factors for Abdominal Aortic Aneurysms: A 7Year Prospective Study: The Tromsø Study, 1994–2001. Circulation 2009;119:2202-8.

20.

Sweeting M, Thompson S, Brown L, et al. Meta-analysis of individual patient data to

256

examine factors affecting growth and rupture of small abdominal aortic aneurysms. Br J Surg

257

2012; 99:655-65.

258

21.

Brown LC, Powell JT. Risk factors for aneurysm rupture in patients kept under ultrasound 11

ACCEPTED MANUSCRIPT 259

22.

261 262

and its role in the symptomatology of aneurysm. Cytokines Cell Mol Ther 2002;7:91-7. 23.

263 264

Treska V, Kocova J, Boudova L, et al. Inflammation in the wall of abdominal aortic aneurysm

Nordon IM, Hinchliffe RJ, Loftus IM, et al. Pathophysiology and epidemiology of abdominal aortic aneurysms. Nat Rev Cardiol 2011;8:92-102.

24.

RI PT

260

surveillance. UK Small Aneurysm Trial Participants. Ann Surg 1999;230:289-96.

Jin J, Arif B, Garcia-Fernandez F, et al. Novel mechanism of aortic aneurysm development in mice associated with smoking and leukocytes. Arterioscler Thromb Vasc Biol 2012;32:2901-

266

9. 25.

268

acetylcholine receptors. Mediators Inflamm 2012;2012:103120. 26.

270 271

27.

Ronksley PE, Brien SE, Turner BJ, et al. Association of alcohol consumption with selected cardiovascular disease outcomes: a systematic review and meta-analysis. BMJ 2011; 342.

28.

274 275

Hendel A, Ang LS, Granville DJ. Inflammaging and proteases in abdominal aortic aneurysm. Curr Vasc Pharmacol 2015;13:95-110.

272 273

M AN U

269

Li ZZ, Dai QY. Pathogenesis of abdominal aortic aneurysms: role of nicotine and nicotinic

Stackelberg O, Björck M, Larsson SC, et al. Alcohol Consumption, Specific Alcoholic

TE D

267

SC

265

Beverages, and Abdominal Aortic Aneurysm. Circulation 2014;130:646-52. 29.

Taylor B, Irving HM, Baliunas D, et al. Alcohol and hypertension: gender differences in dose–response relationships determined through systematic review and meta-analysis.

277

Addiction 2009;104:1981-90. 30.

279

atherosclerosis: the Multi-Ethnic Study of Atherosclerosis. Eur J Vasc Endovasc Surg 201;

280 281

41:481-7.

31.

282 283 284

Laughlin GA, Allison MA, Jensky NE, et al. Abdominal aortic diameter and vascular

AC C

278

EP

276

Wong DR, Willett WC, Rimm EB. Smoking, hypertension, alcohol consumption, and risk of abdominal aortic aneurysm in men. Am J Epidemiol 2007;165:838-45.

32.

Yoon YS, Oh SW, Baik HW, et al. Alcohol consumption and the metabolic syndrome in Korean adults: the 1998 Korean National Health and Nutrition Examination Survey. Am J 12

ACCEPTED MANUSCRIPT 285

Clin Nutr 2004;80:217-24.

286 287

RI PT

288 289

SC

290

M AN U

291 292 293

297 298 299 300

EP

296

AC C

295

TE D

294

301 302

13

ACCEPTED MANUSCRIPT 303

Table I. Prevalence of abdominal aortic aneurysm Characteristics Total

Screening (%) 2,035 (100)

AAA (%) 22 (1.1)

908 (44.6)

18 (2.0)

female

1,127 (55.4)

4 (0.4)

< 50

94 (4.6)

0 (0)

50-59

382 (18.8)

3 (0.8)

60-69

633 (31.1)

70-79

744 (36.6)

≥80

182 (8.9)

307 308 309 310

M AN U

TE D

4 (2.2)

EP

306

11 (1.5)

AC C

305

AAA = abdominal aortic aneurysm

4 (0.6)

311 312

14

SC

male

Age (years)

304

RI PT

Sex

ACCEPTED MANUSCRIPT

Frequency (%)

Hypertension

998 (49.0)

Smoking

759 (37.3)

Alcohol

749 (36.8)

Hyperlipidemia

577 (28.4)

Diabetes

387 (19.0)

Coronary artery disease*

196 (9.6)

Cerebrovascular disease†

130 (6.4)

Pulmonary disease‡

52 (2.6)

End-stage renal disease

22 (1.1)

* Mainly ischemic heart disease

315

† Including transient ischemic attack, reversible ischemic

319 320

‡ Mainly chronic obstructive pulmonary disease

EP

318

neurologic deficit, and stroke

AC C

317

TE D

314

316

SC

Risk factors

RI PT

Table II. Risk factors in the screened population

M AN U

313

15

ACCEPTED MANUSCRIPT 321

Table III. Univariate analysis of risk factors for abdominal aortic aneurysm Risk factors

Variable (%)

Sex

Male (2.0)

P value* <0.001

< 50 (0); 50s (0.7); 60s (0.7); 70s (1.5); 80 < (2.8)

Smoking

Non-smoker (0.4) Ex-smoker (1.6)

No (0.5); yes (2.0)

<0.01

Body mass index (≥ 25kg/m2)

No (1.0); yes (1.1)

0.81

Diabetes

No(1.0); yes(1.3)

0.59

Hypertension

No(1.0); yes(1.2)

0.60

Coronary artery disease

No (0.8); yes (1.7)

0.07

No (1.0); yes (1.5)

0.46

No (1.0); yes (5.9)

0.01

EP

Pulmonary disease

TE D

Alcohol

Hyperlipidemia

323 324

Cerebrovascular disease

No (1.1); yes (0.8)

1.00

End-stage renal disease

No (1.1); yes (0)

1.00

AC C

322

<0.001

M AN U

Current-smoker (8.0)

0.01

SC

Age

RI PT

Female (0.4)

* Chi-square test

325 326 16

ACCEPTED MANUSCRIPT Table IV. Multivariate analysis of risk factors for abdominal aortic aneurysm 95% CI

P value*

Male sex

1.7

0.35 - 8.57

0.49

Age per 10 year

0.6

0.18 - 1.99

0.40

Smoking

7.4

2.55 - 21.47

Alcohol

0.6

0.21 - 1.88

Pulmonary disease

3.0

0.63 - 14.55

<0.001 0.40

0.16

EP

TE D

M AN U

* Multiple logistic regression analysis

AC C

328

Odd ratio

RI PT

Risk factors

SC

327

17