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血管紧张素转换酶基因多态性与轻至中度原发性高血压患者轻度运动疗法降压反应的相关性

Association of angiotensin-converting-enzyme gene polymorphism with the depressor response to mild exercise therapy in patients with mild to moderate essential hypertension.

作者信息

Zhang B, Sakai T, Miura S, Kiyonaga A, Tanaka H, Shindo M, Saku K

机构信息

Department of Cardiology, Fukuoka University School of Medicine, Fukuoka, Japan.

出版信息

Clin Genet. 2002 Oct;62(4):328-33. doi: 10.1034/j.1399-0004.2002.620414.x.

DOI:10.1034/j.1399-0004.2002.620414.x
PMID:12372063
Abstract

We studied the association of angiotensin I-converting enzyme (ACE) gene polymorphism with the depressor response to exercise therapy in 64 Japanese subjects with mild to moderate essential hypertension. Each subject performed 10 weeks of mild (lactate threshold intensity: approximately 50% maximum oxygen consumption) exercise therapy on a bicycle ergometer. Systolic blood pressure (SPB), diastolic blood pressure (DPB), and mean arterial pressure (MAP) were significantly decreased by exercise therapy in subjects with the ACE-II and ID genotypes but not in DD subjects. The time-by-genotype interaction effects were significant for DBP and MAP. According to a multiple logistic regression analysis, the age- and baseline plasma renin activity-adjusted relative risk (odds ratio) for the lack of a depressor response conferred by the D allele (assuming an additive effect) was 2.72 [95% confidence interval (CI), 1.07-6.91; p = 0.034]; for DD genotypes, as compared with the DI and II genotypes (assuming that the D allele is recessive), it was 11.7 (95% CI, 2.25-60.6; p = 0.003). ACE gene I/D polymorphism is associated with the depressor response of essential hypertensives to mild exercise therapy, which suggests that genetic features may underlie, at least in part, the heterogeneity of the depressor response in essential hypertensives to mild exercise therapy.

摘要

我们研究了64名轻度至中度原发性高血压日本受试者中血管紧张素I转换酶(ACE)基因多态性与运动疗法降压反应之间的关联。每位受试者在自行车测力计上进行了10周的轻度(乳酸阈值强度:约为最大耗氧量的50%)运动疗法。ACE-II和ID基因型受试者的收缩压(SPB)、舒张压(DPB)和平均动脉压(MAP)通过运动疗法显著降低,而DD基因型受试者则未降低。DBP和MAP的时间-基因型交互作用显著。根据多元逻辑回归分析,D等位基因(假设为加性效应)导致缺乏降压反应的年龄和基线血浆肾素活性调整后的相对风险(比值比)为2.72 [95%置信区间(CI),1.07 - 6.91;p = 0.034];对于DD基因型,与DI和II基因型相比(假设D等位基因为隐性),为11.7(95% CI,2.25 - 60.6;p = 0.003)。ACE基因I/D多态性与原发性高血压患者对轻度运动疗法的降压反应相关,这表明遗传特征可能至少部分地是原发性高血压患者对轻度运动疗法降压反应异质性的基础。

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