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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Association of endothelial nitric oxide synthase (eNOS) gene G894T polymorphism with hypertension risk and complications
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Association of endothelial nitric oxide synthase (eNOS) gene G894T polymorphism with hypertension risk and complications

机译:内皮一氧化氮合酶(ENOS)基因G894T多态性与高血压风险和并发症的关联

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摘要

This study evaluated the association of NOS3 polymorphisms with hypertension risk and complications. eNOS (G894T) SNP was performed by RT-PCR on 70 hypertensive patients (25 were hypertensive, 25 were hypertensive with CAD, and 20 were diabetic with hypertension) and 30 age- and gender-matched individuals. Lipid and glucose profile were assessed by standard colorimetric assay. Our results revealed that combination of (GT + TT) genotype and T allele significantly increases the risk of hypertension (OR = 3.86 and 4.33), respectively. Subgroup analysis showed significant association between CAD with eNOS (G894T) mutant genotype (P = 0.002) and allele frequency (P < 0.001). Moreover, the mutant homozygous and heterozygous eNOS genotype together were significantly associated with higher TC, LDLc, (P < 0.001), and TG (P = 0.001). Thus, hypercholesterolemia (P < 0.001 and OR = 12.48) increases the risk of hypertension among T carrier. These results indicated that the T carriers significantly increase hypertension risk and complication (CAD), mainly with hypercholesterolemia and in elderly.
机译:该研究评估了NOS3多态性与高血压风险和并发症的关联。 eNOS(G894T)SNP通过RT-PCR在70名高血压患者(25名高血压,25例与CAD高血压,20例糖尿病患者高血压)和30岁和性别匹配的个体。通过标准比色测定评估脂质和葡萄糖曲线。我们的研究结果表明,(GT + TT)基因型和T等位基因的组合分别显着增加了高血压(或= 3.86和4.33)的风险。亚组分析显示CAD与eNOS(G894T)突变基因型(P = 0.002)和等位基因频率之间的显着关联(P <0.001)。此外,突变纯合和杂合烯烯型基因型与较高的TC,LDLC(P <0.001)和TG(P = 0.001)显着相关。因此,高胆固醇血症(P <0.001和= 12.48)增加了T载体中高血压的风险。这些结果表明,T载体显着增加高血压风险和复杂性(CAD),主要是具有高胆固醇血症和老年人。

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