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脂联素基因多态性与冠状动脉疾病关联的最新系统评价和荟萃分析

An Updated Systematic Review and Meta-analysis of Association Between Adiponectin Gene Polymorphisms and Coronary Artery Disease.

作者信息

Hou Haifeng, Ge Siqi, Zhao Linlin, Wang Chenglin, Wang Wei, Zhao Xuezhen, Sun Zheng

机构信息

1 Taishan Medical University , Taian, Shandong, P.R. China .

2 School of Medical and Health Sciences, Edith Cowan University , Perth, Australia .

出版信息

OMICS. 2017 Jun;21(6):340-351. doi: 10.1089/omi.2017.0007.

Abstract

Coronary artery disease (CAD) is a significant contributor to global health burden. Adiponectin gene single nucleotide polymorphisms (SNPs) have been associated with CAD susceptibility, but with inconsistent results across the studies. We present, in this study, an updated meta-analysis to discern the genetic susceptibility of adiponectin SNPs in relation to CAD. PubMed and EMBASE databases were used to identify the relevant published articles using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Pooled odds ratios and 95% confidence intervals were generated to assess the strength of the associations. Thirty-five articles with a total of 28,947 participants (mean age 55.3 years, 11,632 cases/17,315 controls, 19,443 males/8353 females, and 1151 persons with unspecified gender data) were included. The dominant, recessive, and additive models were applied. We found that the SNPs +45T>G (rs2241766), -4034A>C (rs822395), and -11391G>A (rs17300539) were linked to CAD development. In addition, +276G>T (rs1501299) SNP was associated with a decreased susceptibility to CAD among Caucasians. We did not find an association between the CAD susceptibility and the -11377C>G (rs266729) SNP. These observations offer new potential genetic biomarker candidates in relation to CAD, and warrant further research in independent world populations.

摘要

冠状动脉疾病(CAD)是全球健康负担的重要促成因素。脂联素基因单核苷酸多态性(SNP)与CAD易感性相关,但各研究结果不一致。在本研究中,我们进行了一项更新的荟萃分析,以识别脂联素SNP与CAD相关的遗传易感性。使用PubMed和EMBASE数据库,按照系统评价和荟萃分析的首选报告项目(PRISMA)指南识别相关已发表文章。生成合并比值比和95%置信区间以评估关联强度。纳入了35篇文章,共28,947名参与者(平均年龄55.3岁,11,632例/17,315例对照,19,443名男性/8353名女性,1151人性别数据未明确)。应用显性、隐性和加性模型。我们发现SNP +45T>G(rs2241766)、-4034A>C(rs822395)和-11391G>A(rs17300539)与CAD发生有关。此外,+276G>T(rs1501299)SNP与白种人中CAD易感性降低有关。我们未发现CAD易感性与-11377C>G(rs266729)SNP之间存在关联。这些观察结果提供了与CAD相关的新的潜在遗传生物标志物候选物,值得在独立的全球人群中进行进一步研究。

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