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内皮型一氧化氮合酶基因与冠状动脉疾病相关:一项荟萃分析。

The endothelial nitric oxide synthase gene is associated with coronary artery disease: a meta-analysis.

作者信息

Li Junyan, Wu Xinxing, Li Xingwang, Feng Guoyin, He Lin, Shi Yongyong

机构信息

Bio-X Center and Affiliated Changning Mental Health Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, PR China.

出版信息

Cardiology. 2010;116(4):271-8. doi: 10.1159/000316063. Epub 2010 Sep 22.

Abstract

INTRODUCTION

Previous case-control studies have suggested that the endothelial nitric oxide synthase (eNOS) gene polymorphisms (G894T, 4b/a, T-786C) are associated with coronary artery disease (CAD). However, other studies do not confirm these relationships. The objective was to assess these relationships using meta-analysis.

METHODS

Databases, including Pubmed and Embase, were searched to access the relevant genetic association studies up to July 2009.

RESULTS

The meta-analysis included 56 studies, consisting of 23 studies for G894T, 19 for 4b/a and 14 for T-786C. For the allelic analysis of the G894T variant, all studies showed a positively significant association (OR = 0.83, p = 0.004). For the genotypic analysis, the combined studies of the T allele showed significance (OR = 1.57, p = 0.003). For the allelic analysis of the T-786C variant, all studies showed an obviously significant association (OR = 0.79, p = 0.0007), reflected in both non-Asian and Asian studies. For the genotype analysis, combined studies of the C allele showed significance (OR = 0.72, p = 0.0001). Moreover, non-Asian studies showed significant results. For the analysis of the 4b/a variant, none of the studies showed significant results. No publication bias was found in the meta-analysis.

CONCLUSION

The synthesis of available evidence supports the fact that eNOS G894T andT-786C are associated with CAD.

摘要

引言

先前的病例对照研究表明,内皮型一氧化氮合酶(eNOS)基因多态性(G894T、4b/a、T - 786C)与冠状动脉疾病(CAD)相关。然而,其他研究并未证实这些关系。本研究目的是通过荟萃分析评估这些关系。

方法

检索包括Pubmed和Embase在内的数据库,以获取截至2009年7月的相关基因关联研究。

结果

荟萃分析纳入了56项研究,其中G894T相关研究23项,4b/a相关研究19项,T - 786C相关研究14项。对于G894T变异的等位基因分析,所有研究均显示出显著正相关(OR = 0.83,p = 0.004)。对于基因型分析,T等位基因的合并研究具有显著性(OR = 1.57,p = 0.003)。对于T - 786C变异的等位基因分析,所有研究均显示出明显的显著关联(OR = 0.79,p = 0.0007),在非亚洲和亚洲研究中均有体现。对于基因型分析,C等位基因的合并研究具有显著性(OR = 0.72,p = 0.0001)。此外,非亚洲研究显示出显著结果。对于4b/a变异的分析,没有研究显示出显著结果。荟萃分析未发现发表偏倚。

结论

现有证据的综合支持了eNOS G894T和T - 786C与CAD相关这一事实。

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