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肾素-血管紧张素系统多态性与突尼斯人群的高血压状况和肥胖的关系。

Renin-angiotensin system polymorphisms in relation to hypertension status and obesity in a Tunisian population.

机构信息

Laboratory of Nutrition and Vascular Health, Faculty of Medicine, Monastir, Tunisia.

出版信息

Mol Biol Rep. 2012 Apr;39(4):4059-65. doi: 10.1007/s11033-011-1187-2. Epub 2011 Jul 21.

Abstract

Essential hypertension (HTA) is the clinical expression of a disordered interaction between the genetic, physiological, and biochemical systems that under usual conditions maintain cardiovascular homeostasis. We studied the effects of the angiotensinogen M235T, angiotensin converting enzyme insertion/deletion (ACE I/D), and angiotensin II receptor 1 (AT1R) A1166C gene polymorphisms on the risk of HTA and to evaluate the relationship between these polymorphisms and obesity. We performed AGT, ACE and AGTR genotyping in 142 hypertensive patients and 191 control subjects using PCR-RFLP methods and PCR, respectively. The three polymorphisms were significantly associated with HTA. Individuals carrying the mutated TT of AGT, DD of ACE and CC of AT1R genotypes had an 1.67 (P = 0.032), 3.09 (P < 0.001) and 3.45 (P < 0.001)-fold increased risk of HTA. After adjustment for sex, smoking, diabetes, dyslipidemia, BMI, triglycerides and DD, TT and CC genotypes, BMI was independent risk factor of HTA (OR = 3.14; P < 0.001). An association of BMI with ACE gene polymorphism (P = 0.035), whereas no association with AGT and AT1R gene polymorphisms was obtained. The proportion of hypertensives is as high as 21.8 and 13.4% in the overweight and the obese DD group. The present study implies that the genotyping for the variants of RAS gene could in the future become an important part of the clinical process of risk identification for HTA.

摘要

原发性高血压(HTA)是遗传、生理和生化系统之间失调相互作用的临床表现,这些系统在通常情况下维持心血管内环境稳定。我们研究了血管紧张素原 M235T、血管紧张素转换酶插入/缺失(ACE I/D)和血管紧张素 II 受体 1(AT1R)A1166C 基因多态性对 HTA 风险的影响,并评估了这些多态性与肥胖之间的关系。我们使用 PCR-RFLP 方法和 PCR 分别在 142 例高血压患者和 191 例对照中进行了 AGT、ACE 和 AGTR 基因分型。这三种多态性与 HTA 显著相关。携带 AGT 突变 TT、ACE 突变 DD 和 AT1R 突变 CC 基因型的个体发生 HTA 的风险分别增加 1.67 倍(P=0.032)、3.09 倍(P<0.001)和 3.45 倍(P<0.001)。在调整性别、吸烟、糖尿病、血脂异常、BMI、甘油三酯和 DD、TT 和 CC 基因型后,BMI 是 HTA 的独立危险因素(OR=3.14;P<0.001)。BMI 与 ACE 基因多态性之间存在关联(P=0.035),而与 AGT 和 AT1R 基因多态性之间无关联。超重和肥胖 DD 组的高血压患病率分别高达 21.8%和 13.4%。本研究表明,RAS 基因变异的基因分型可能成为未来 HTA 风险识别临床过程的重要组成部分。

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