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(Hypertension. 2000;36:808.)
© 2000 American Heart Association, Inc.

Scientific Contributions

Renin-Angiotensin System Polymorphisms and Coronary Events in Familial Hypercholesterolemia

Anthony S. Wierzbicki; Michelle Lambert-Hammill; Peter J. Lumb; Martin A. Crook

From the Lipid Unit, Department of Chemical Pathology, King’s College, London (Guy’s, King’s, and St Thomas’ Medical School), St Thomas’ Hospital Campus, London, UK.

Correspondence to Dr A.S. Wierzbicki, Department of Chemical Pathology, St Thomas’ Hospital, Lambeth Palace Rd, London SE1 7EH, UK.

Abstract—The role of renin-angiotensin system polymorphisms as risk factors for coronary heart disease (CHD) is controversial. This study investigated their role in patients with heterozygous familial hypercholesterolemia (FH). Polymorphism frequencies for angiotensin-I–converting enzyme insertion/deletion (ACE I/D), angiotensinogen M235T, and angiotensin-II type I receptor (AG2R) A1166C were determined in 112 patients with FH and 72 patients with polygenic hypercholesterolemia, of whom 26.7% and 41.6%, respectively, had established CHD. None of the polymorphisms were associated with risk of CHD in patients with polygenic hypercholesterolemia in this study. Logistic regression analysis of risk factors for CHD in patients with FH identified male sex (odds ratio [OR]=3.03; 95% CI, 3.07 to 3.72; P=0.05), smoking (OR=2.91; 95% CI, 2.16 to 4.24; P=0.05), diastolic blood pressure (OR=3.70; 95% CI, 3.43 to 3.97; P=0.02), plasma glucose (OR=3.31; 95% CI, 3.10 to 3.52; P=0.04), and the AG2R A1166C polymorphism as risk factors. The OR for the AG2R A1166C polymorphism was 2.26 (95% CI, 1.26 to 3.72; P=0.06) and increased to 3.10 (95% CI, 1.20 to 7.52; P=0.04) after adjustment for other risk factors. The AG2R A1166C polymorphism may interact with severe hypercholesterolemia and other risk factors to increase risk of CHD in FH patients.

Key Words: familial hypercholesterolemia • coronary artery disease • renin-angiotensin system • genetics

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