(Hypertension. 2002;39:1053.)
© 2002 American Heart Association, Inc.
Scientific Contributions |
From the Human Genetics Center, University of TexasHouston Health Science Center (A.C.M., M.S.B., E.B.), Houston; Division of Epidemiology, School of Public Health, University of Minnesota (A.R.F.), Minneapolis; and Institute of Molecular Medicine (E.B.), Houston, Tex.
Correspondence to Eric Boerwinkle, PhD, Human Genetics Center, University of TexasHouston Health Science Center, 1200 Herman Pressler; Suite 453E, Houston, TX 77030. E-mail Eric.Boerwinkle@ uth.tmc.edu
Abstract High blood pressure is a predictor of cardiovascular disease. Hence, genes contributing to essential hypertension may play a role in the etiology of cardiovascular disease. For this reason, we examined the association between the
-adducin (ADD1) G460W and G-protein ß3 subunit (GNB3) 825C>T polymorphisms and the prevalence of peripheral arterial disease (PAD) and incidence of coronary heart disease (CHD) in non-Hispanic whites from the Atherosclerosis Risk in Communities (ARIC) Study. PAD prevalence was defined by an ankle-brachial index, ie, the ratio of ankle systolic blood pressure to brachial artery systolic blood pressure, of
0.90 for men and
0.85 for women. CHD incidence was determined by following the ARIC cohort for a median of 5.3 years for potential coronary events. Stratified random samples of the ARIC cohort (n=703 and n=684) were used, respectively, as the comparison groups for the PAD (n=144) and incident CHD (n=408) cases. The GNB3 825T allele and the ADD1 460W allele were not significantly associated with prevalence of PAD or incidence of CHD. However, a test of the interaction between hypertension status and the ADD1 G460W polymorphism indicated that further evaluation of the ADD1 polymorphism in only hypertensive individuals was warranted. The ADD1 460W allele was significantly associated with PAD (odds ratio [OR]: 2.61, 95% CI, 1.275.37, P=0.01) and CHD (hazard rate ratio [HRR]: 2.30, 95% CI, 1.204.42, P=0.01) in hypertensive individuals after adjustment for multiple cardiovascular disease risk factors. An interaction with hypertension in the association between the ADD1 G460W polymorphism and cardiovascular disease merits further testing in additional populations.
Key Words: genetics risk factors polymorphism hypertension, essential cardiovascular diseases
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