4.8 Article

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

期刊

CIRCULATION
卷 109, 期 3, 页码 335-339

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.CIR.0000109487.46725.02

关键词

genetics; calcium; atherosclerosis

资金

  1. NHLBI NIH HHS [R01-HL69126, N01-HC-48047, N01-HC-95095, N01-HC-48050, N01-HC-48049, N01-HC-48048] Funding Source: Medline
  2. NINDS NIH HHS [NS41466] Funding Source: Medline

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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.

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