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首页> 外文期刊>Journal of Renin-Angiotensin-Aldosterone System >The interaction of AGT and NOS3 gene polymorphisms with conventional risk factors increases predisposition to hypertension
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The interaction of AGT and NOS3 gene polymorphisms with conventional risk factors increases predisposition to hypertension

机译:AGT和NOS3基因多态性与常规危险因素的相互作用增加了高血压的易感性

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Renin-angiotensin and kallikrein-kinin systems are interconnected, regulating blood pressure homeostasis. We have demonstrated the interactions among polymorphisms of the angiotensinogen (AGT) and endothelial nitric oxide synthase (NOS3) genes and conventional risk factors affecting the hypertension occurrence. Individuals were recruited (n=192) and classified into hypertensive (HG; n=140) and normotensive (NG; n=52) groups. The genotypic distribution of the Met235Thr (AGT) and Glu298Asp (NOS3) polymorphisms demonstrated that both are independent risk factors of hypertension (p=0.02 and p=0.008, respectively). The concomitant presence of these polymorphisms in the HG group was significantly different (p=0.001) from the NG. Both gene polymorphisms presented an additive effect for the unfavourable alleles T and A, respectively, and 95% of the double mutant homozygotes were classified into the HG. Specific interactions among certain conventional factors and the presence of at least one unfavourable allele presented significant odds towards hypertension. Blood pressure homeostasis was affected by genetic polymorphisms conditioned by the T and A alleles of the AGT and NOS3 genes, respectively, which acted independently. However, their interaction with smoking, sedentariness, age and total cholesterol may have increased the predisposition to hypertension, which may explain most of the hypertension cases.
机译:肾素-血管紧张素和激肽释放酶-激肽系统相互连接,调节血压稳态。我们已经证明了血管紧张素原(AGT)和内皮型一氧化氮合酶(NOS3)基因的多态性与影响高血压发生的常规危险因素之间的相互作用。招募个体(n = 192)并分为高血压(HG; n = 140)和血压正常(NG; n = 52)组。 Met235Thr(AGT)和Glu298Asp(NOS3)多态性的基因型分布表明,两者都是高血压的独立危险因素(分别为p = 0.02和p = 0.008)。 HG组中这些多态性的同时存在与NG显着不同(p = 0.001)。两种基因多态性分别对不利的等位基因T和A表现出加和作用,并且95%的双突变纯合子被归类为HG。某些常规因素之间的特异性相互作用以及至少一种不利的等位基因的存在为高血压带来了巨大的可能性。血压的稳态受到分别由AGT和NOS3基因的T和A等位基因调节的遗传多态性的影响,它们独立发挥作用。然而,它们与吸烟,久坐,年龄和总胆固醇的相互作用可能增加了高血压的易感性,这可以解释大多数高血压病例。

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