Endothelial nitric oxide synthase gene (NOS3) variant and hypertension in pregnancy

被引:31
作者
Kobashi, G
Yamada, H
Ohta, K
Kato, EH
Ebina, Y
Fujimoto, S
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Prevent Med, Sapporo, Hokkaido, Japan
[2] Hokkaido Univ, Grad Sch Med, Dept Obstet & Gynecol, Sapporo, Hokkaido, Japan
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 103卷 / 03期
关键词
hypertension; pregnancy; preeclampsia; endothelial nitric oxide synthase gene; angiotensinogen gene; variant;
D O I
10.1002/ajmg.1535
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hypertension in pregnancy (HP), including preeclampsia, is known to be a multifactorial disease. Recently, a Glu298Asp variant of the endothelial nitric oxide synthase gene (NOS3) was identified as being associated with coronary spasm and myocardial infarction, whereas it has been reported that endothelial nitric oxide synthase plays a role in HP. We therefore performed an association study of the Glu298Asp variant with HP among 152 H-P patients and 335 normal pregnant control individuals, in the context of other risk factors before pregnancy. The frequency of the variant GA+AA NOS3 genotypes was significantly higher in the patients (0.23) than in the controls (0.12) (P <0.01). Multivariate analysis revealed that family history of hypertension, TT genotype of the angiotensinogen gene (AGT), GA+AA NOS3 genotype, and prepregnancy body mass index greater than or equal to 24 were independent potent risk factors, after adjustment for maternal age and parity. The odds ratios of the factors were 2.7, 2.3, 2.2, and 2.1, respectively. Our results suggested that the Asp298 of NOS3 is a potent, independent risk factor for HP. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:241 / 244
页数:4
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