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髓过氧化物酶基因多态性与冠状动脉疾病易感性的Meta分析

Meta-analysis of myeloperoxidase gene polymorphism and coronary artery disease susceptibility.

作者信息

Chen Luyao, Zhao Shushan, Cheng Guangjie, Shi Ruizheng, Zhang Guogang

机构信息

Department of Cardiology, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2014 Mar;39(3):217-31. doi: 10.11817/j.issn.1672-7347.2014.03.001.

Abstract

OBJECTIVE

To assess the association between myeloperoxidase (MPO) gene polymorphism and coronary artery disease (CAD).

METHODS

Several databases were used to retrieve relevant literature up to March 2013 by keywords. A Meta-analysis was performed by Stata12.0 software to estimate the pooled odds ratio (OR) and the 95% confidence interval (CI). Heterogeneity among studies was tested and sensitivity analysis was applied. Publication bias was examined using Begg's funnel plot and Egger's linear regression test.

RESULTS

A total of 17 studies were included in this Meta-analysis. For MPO -463 G/A polymorphism, the pooled OR of A allele vs G allele was 0.58 [95% CI (0.47-0.72)] and the pooled OR of genotypes AA+AG vs GG was 0.58 [95% CI (0.46-0.72)]. In subgroup analysis of study population, AA and AG genotypes were significantly associated with CAD in Asians but not in Europeans. The MPO -463 G/A polymorphism in the stable angina pectoris subgroup was evaluated in 3 studies and the pooled OR of A allele vs G allele and genotypes AA+AG vs GG for proven CAD was 0.45 [95% CI (0.15-1.37)] and 0.57 [95% CI (0.19- 1.65)]. For MPO -129 A/G gene polymorphism, the pooled OR of genotype GG vs AA+AG was 0.91 [95% CI (0.74-1.10)].

CONCLUSION

A allele of MPO -463 G/A gene is associated with decreased risk of CAD except in the Europeans. There is no association between MPO -129 A/G gene polymorphisms and CAD risk.

摘要

目的

评估髓过氧化物酶(MPO)基因多态性与冠状动脉疾病(CAD)之间的关联。

方法

通过关键词检索截至2013年3月的多个数据库中的相关文献。使用Stata12.0软件进行Meta分析,以估计合并优势比(OR)和95%置信区间(CI)。检验研究间的异质性并进行敏感性分析。使用Begg漏斗图和Egger线性回归检验检查发表偏倚。

结果

本Meta分析共纳入17项研究。对于MPO -463 G/A多态性,A等位基因与G等位基因的合并OR为0.58 [95%CI(0.47 - 0.72)],基因型AA + AG与GG的合并OR为0.58 [95%CI(0.46 - 0.72)]。在研究人群的亚组分析中,AA和AG基因型在亚洲人与CAD显著相关,但在欧洲人中并非如此。在3项研究中评估了稳定型心绞痛亚组中的MPO -463 G/A多态性,对于确诊的CAD,A等位基因与G等位基因以及基因型AA + AG与GG的合并OR分别为0.45 [95%CI(0.15 - 1.37)]和0.57 [95%CI(0.19 - 1.65)]。对于MPO -129 A/G基因多态性,基因型GG与AA + AG的合并OR为0.91 [95%CI(0.74 - 1.10)]。

结论

MPO -463 G/A基因的A等位基因与CAD风险降低相关,但欧洲人除外。MPO -129 A/G基因多态性与CAD风险之间无关联。

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