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

机译:突尼斯人群中肾素-血管紧张素系统多态性与高血压状态和肥胖的关系

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摘要

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.
机译:原发性高血压(HTA)是遗传,生理和生化系统之间相互作用紊乱的临床表现,在通常情况下维持心血管稳态。我们研究了血管紧张素原M235T,血管紧张素转化酶插入/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。我们分别使用PCR-RFLP方法和PCR对142例高血压患者和191例对照受试者进行了AGT,ACE和AGTR基因分型。这三个多态性与HTA显着相关。携带突变型AGT的TT,ACE的DD和AT1R基因型的CC的个体发生HTA的风险增加了1.67(P = 0.032),3.09(P <0.001)和3.45(P <0.001)。在调整了性别,吸烟,糖尿病,血脂异常,BMI,甘油三酸酯以及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基因多态性相关(P = 0.035),而未与AGT和AT1R基因多态性相关。在超重和肥胖DD组中,高血压的比例高达21.8%和13.4%。本研究表明,RAS基因变异的基因分型将来可能成为HTA风险识别临床过程的重要组成部分。

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