Lack of Evidence for Association Between the Endothelial Nitric Oxide Synthase Gene and Hypertension

Author:

Kato Norihiro1,Sugiyama Takao1,Morita Hiroyuki1,Nabika Toru1,Kurihara Hiroki1,Yamori Yukio1,Yazaki Yoshio1

Affiliation:

1. From the Graduate School of Human and Environmental Studies, University of Kyoto (N.K., Y.Y.); The Institute for Adult Diseases Asahi Life Foundation, Tokyo (T.S.); the Department of Cardiovascular Medicine, Graduate School of Medicine, University of Tokyo (H.M., H.K., Y.Y.); and the Department of Laboratory Medicine, Shimane Medical University (T.N.).

Abstract

Abstract —Significant association between a Glu298Asp polymorphism of the endothelial nitric oxide synthase (eNOS) gene and essential hypertension was recently reported in Japanese populations, with the 298Asp variant showing a higher prevalence in hypertensive patients (10.3% to 12.0%) than in normotensive subjects (5.0% to 5.8%). In contrast, another study demonstrated that the 298Glu variant was significantly associated with hypertension in a Caucasian population. We therefore undertook an extensive association study in Japanese to resolve these contradictory claims. A total of 1165 individuals were selected from clinic outpatients and hospital staff in a single institution. The relevance of the Glu298Asp polymorphism to hypertension in this population was tested in 2 ways. First, a case-control study was conducted in 549 hypertensive and 513 normotensive subjects within the study population, with the χ 2 statistic used to test the significance of an association between eNOS genotype and the presence of hypertension. Second, an ANOVA was used to test the significance of an association between eNOS genotype and the level of blood pressure within the entire population except for 167 hypertensive subjects who had been under treatment for hypertension. No significant association was observed in either of the statistics tested. Allele frequencies of 298Asp were concordant across the panels: 8.4% in hypertensive subjects, 8.2% in normotensive subjects, and 7.9% and 9.5% in 2 additional sample populations used as reference panels. Taken together, our results do not support the previous observation that the molecular variant of the eNOS gene may confer principal susceptibility for essential hypertension but rather suggest the existence of sampling variation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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