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Endothelial nitric oxide synthase gene polymorphisms and essential hypertension in Han Chinese

机译:汉族人内皮型一氧化氮合酶基因多态性与原发性高血压

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摘要

We examined the effect of polymorphisms in the endothelial nitric oxide synthase gene on the risk for essential hypertension in a Han Chinese population through a meta-analysis of data from 15 studies. Associations between increased risk for essential hypertension and 4b/a were obtained in a dominant model and allele contrast (aa + ab vs bb: odds ratio (OR)FE = 1.26, 95% confidence interval (CI) = 1.10-1.44; a vs b allele: ORFE = 1.23, 95%CI: 1.09-1.40). Four studies with sample sizes over 500 produced similar results. No evidence of publication bias was found. Also, no significant heterogeneity was observed among these studies. When we examined the G894T polymorphism, we found a marginally significant association for allele contrast and the recessive model when all the eligible studies were pooled together. However, there was no evidence for a significant association after the exclusion of two studies deviating from Hardy-Weinberg equilibrium in the control group. Heterogeneity among studies was observed. Results of cumulative and recursive cumulative meta-analysis indicated that more studies are needed to objectively determine the effects of these two polymorphisms.
机译:我们通过对15项研究数据的荟萃分析,检查了内皮型一氧化氮合酶基因多态性对汉族人群原发性高血压风险的影响。在显性模型和等位基因对比中获得了原发性高血压风险增加与4b / a之间的相关性(aa + ab vs bb:优势比(OR)FE = 1.26,95%置信区间(CI)= 1.10-1.44; b等位基因:ORFE = 1.23,95%CI:1.09-1.40)。样本量超过500的四项研究得出了相似的结果。没有发现出版偏见的证据。同样,在这些研究中没有观察到明显的异质性。当我们检查G894T多态性时,我们将所有符合条件的研究汇总在一起,发现等位基因对比和隐性模型之间的边际显着关联。但是,在排除两组偏离哈迪-温伯格平衡的研究后,没有证据表明存在显着相关性。研究中观察到异质性。累积和递归累积荟萃分析的结果表明,需要更多的研究来客观地确定这两个多态性的影响。

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