Polymorphism of the soluble epoxide hydrolase is associated with coronary artery calcification in African-American subjects - The Coronary Artery Risk Development in Young Adults (CARDIA) study

被引:125
作者
Fornage, M
Boerwinkle, E
Doris, PA
Jacobs, D
Liu, K
Wong, ND
机构
[1] Univ Texas, Hlth Sci Ctr, Inst Mol Med Prevent Human Dis, Houston, TX 77030 USA
[2] Univ Texas, Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USA
[3] Univ Minnesota, Div Epidemiol, Minneapolis, MN 55455 USA
[4] Northwestern Univ, Sch Med, Chicago, IL USA
[5] Univ Calif Irvine, Heart Dis Prevent Program, Irvine, CA USA
关键词
genetics; calcium; atherosclerosis;
D O I
10.1161/01.CIR.0000109487.46725.02
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Modulation of endogenous epoxide levels by soluble epoxide hydrolase (sEH) in the endothelium represents an important mechanism in the regulation of cardiovascular function. We examined the relationship between a common, functional polymorphism of the human sEH gene and coronary artery calcification (CAC) in young, largely asymptomatic African-American and non-Hispanic white subjects. Methods and Results - Multiple logistic regression and Tobit regression models were used to assess the relationship between the sEH Arg287Gln polymorphism and presence and quantity of CAC. Models adjusting for race ( except in race-specific analyses), age, sex, smoking, body mass index, systolic blood pressure, LDL cholesterol, and HDL cholesterol were estimated. Allele and genotype frequency distributions were not significantly different between the 2 ethnic groups ( P = 0.22; P = 0.17, respectively). The Arg287Gln polymorphism of the sEH gene was a significant predictor of CAC status in African-American participants, either alone or after adjusting for other risk factors. African-American subjects with at least 1 copy of the Gln287 allele had a 2-fold greater risk of having CAC compared with those not carrying this allele (95% CI, 1.1 to 2.9; P = 0.02). There was no relationship between Arg287Gln polymorphism and the probability of having CAC in white participants ( OR, 0.8; 95% CI, 0.5 to 1.3; P = 0.49). Inferences from multivariable Tobit regression were similar to those obtained in the logistic regression models, indicating that the Arg287Gln polymorphism was a significant independent predictor of both presence and quantity of CAC in African-American but not white subjects. Conclusions - These data suggest an intriguing and possibly novel role for sEH in the pathogenesis of atherosclerosis, which deserves additional investigation.
引用
收藏
页码:335 / 339
页数:5
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