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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >The G894T polymorphism on endothelial nitric oxide synthase gene is associated with increased coronary heart disease among Asia population: Evidence from a Meta analysis
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The G894T polymorphism on endothelial nitric oxide synthase gene is associated with increased coronary heart disease among Asia population: Evidence from a Meta analysis

机译:内皮型一氧化氮合酶基因的G894T多态性与亚洲人群冠心病的增加有关:来自Meta分析的证据

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摘要

Introduction: Growing studies have revealed the underlying association between eNOS 894 G/T (rs1799983) polymorphism and coronary heart disease (CHD) among Asia population. Results from these studies remained conflicting. We conducted this meta-analysis to estimate the overall CHD risk of eNOS 894 G/T polymorphism regarding Asia population. Materials and methods: Up to October 2011, databases including PubMed, Embase and CNKI (China National Knowledge Infrastructure) were searched to access the relevant genetic association studies. Summary odds ratios and corresponding 95% confidence intervals (CIs) for eNOS 894 G/T polymorphism and CHD risk were estimated using fixed or random-effects models when appropriate. Results: 18 case-control studies with 2,994 cases and 3,130 controls were available for this study, including 13 studies of East-Asia descendents, 5 studies of Non East-Asian descendents. The mean T allele frequency was 0.111 in the East-Asia population and 0.147 in the Non East-Asia population, respectively. The summary OR for CHD associated with the T allele was 1.52 (95% confidence intervals (95%CI), 1.37-1.69) by random effects model. Similarly, significantly increased risks were observed in the East-Asia population (OR = 1.54; 95%CI = 1.35-1.76) and in the Non East-Asia population (OR = 1.48; 95%CI = 1.24-1.77), respectively. Conclusions: This meta-analysis indicated that eNOS 894 G/T polymorphism may play an important role in CHD development among Asia population.
机译:简介:越来越多的研究表明,亚洲人群中eNOS 894 G / T(rs1799983)多态性与冠心病(CHD)之间存在潜在的关联。这些研究的结果仍然相互矛盾。我们进行了这项荟萃分析,以估计亚洲人群中eNOS 894 G / T多态性的总体冠心病风险。材料和方法:截至2011年10月,已检索包括PubMed,Embase和CNKI(中国国家知识基础设施)的数据库,以访问相关的遗传关联研究。适当时,使用固定或随机效应模型估算eNOS 894 G / T多态性和冠心病风险的总比值比和相应的95%置信区间(CIs)。结果:18例病例对照研究,包括2,994例病例和3,130例对照,包括东亚后裔的13项研究,非东亚后裔的5项研究。东亚人群的平均T等位基因频率分别为0.111和非东亚人群的平均T等位基因频率为0.147。通过随机效应模型,与T等位基因相关的CHD的总结OR为1.52(95%置信区间(95%CI),1.37-1.69)。同样,在东亚人群中(OR = 1.54; 95%CI = 1.35-1.76)和非东亚人群中(OR = 1.48; 95%CI = 1.24-1.77),风险也显着增加。结论:这项荟萃分析表明,eNOS 894 G / T基因多态性可能在亚洲人群的冠心病发展中起重要作用。

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