-344C/T variant in the promoter of the aldosterone synthase gene (CYP11B2) is associated with metabolic syndrome in men

被引:20
作者
Russo, Paola
Lauria, Fabio
Loguercio, Maria
Barba, Gianvincenzo
Arnout, Josef
Cappuccio, Francesco P.
De Lorgeril, Michel
Donati, Maria B.
Iacoviello, Licia
Krogh, Vittorio
van Dongen, Martien
Siani, Alfonso
机构
[1] CNR, Inst Food Sci, Unit Epidemiol & Populat Genet, I-83100 Avellino, Italy
[2] Katholieke Univ Leuven, Ctr Mol & Vasc Biol, B-3000 Louvain, Belgium
[3] Warwick Med Sch, Clin Sci Res Inst, Coventry, W Midlands, England
[4] Univ Grenoble 1, UFR Med & Pharm, Lab Nutr Vieillissement & Malad Cardiovasc, UFR Med & Pharm, F-38041 Grenoble, France
[5] Catholic Univ, Ctr High Technol Res & Educ Biomed Sci, Campobasso, Italy
[6] Natl Canc Inst, Nutr Epidemiol Unit, I-20133 Milan, Italy
[7] Maastricht Univ, Dept Epidemiol, Maastricht, Netherlands
关键词
aldosterone synthase; CYP11B2; polymorphism; metabolic syndrome; population study;
D O I
10.1016/j.amjhyper.2006.07.012
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background: The -344C/T variant in the promoter of the aldosterone synthase gene (CYP11B2) has been associated with hypertension and may influence glucose homeostasis and body mass in humans. We assessed the association between this genetic variant and metabolic syndrome in a large sample of European population. Methods: Eight hundred two male/female couples, recruited in the framework of the IMMIDIET study, a survey on cardiovascular risk in Italy, UK, and Belgium, had standardized measurements of body mass index, waist circumference, blood pressure (BP), serum total and HDL-cholesterol, triglycerides, and glucose and were genotyped for the -344C/T variant of CYP11B2. Metabolic syndrome was defined according to the International Diabetes Federation criteria. Results: The prevalence of the metabolic syndrome was 23.9% in men and 14.0% in women. The C allele of the variant was associated with metabolic syndrome in men (P = .002) but not in women. At logistic regression analysis, the odds ratio of metabolic syndrome increased progressively with the number of copies of the C allele (CT: 1.54, 95% CI from 1.01 to 2.35; CC: 2.25, 95% CI from 1.38 to 3.66) as compared with the TT homozygotes, taken as reference genotype. Conclusions: The C allele of -344C/T variant of CYP11B2 increases susceptibility to metabolic syndrome in European men, but not in women, suggesting a pleiotropic role for this gene in modulating cardiovascular risk. Am J Hypertens 2007;20:218-222 (c) 2007 American Journal of Hypertension, Ltd.
引用
收藏
页码:218 / 222
页数:5
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