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纤溶酶原激活物抑制剂-1(PAI-1)-675 4G/5G多态性与糖尿病及糖尿病并发症易感性的关联:一项荟萃分析研究

PAI-1 -675 4G/5G polymorphism in association with diabetes and diabetic complications susceptibility: a meta-analysis study.

作者信息

Xu Kuanfeng, Liu Xiaoyun, Yang Fan, Cui Dai, Shi Yun, Shen Chong, Tang Wei, Yang Tao

机构信息

Department of Endocrinology, the First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

PLoS One. 2013 Nov 5;8(11):e79150. doi: 10.1371/journal.pone.0079150. eCollection 2013.

Abstract

A meta-analysis was performed to assess the association between the PAI-1 -675 4G/5G polymorphism and susceptibility to diabetes mellitus (DM), diabetic nephropathy (DN), diabetic retinopathy (DR) and diabetic coronary artery disease (CAD). A literature-based search was conducted to identify all relevant studies. The fixed or random effect pooled measure was calculated mainly at the allele level to determine heterogeneity bias among studies. Further stratified analyses and sensitivity analyses were also performed. Publication bias was examined by the modified Begg's and Egger's test. Twenty published articles with twenty-seven outcomes were included in the meta-analysis: 6 studies with a total of 1,333 cases and 3,011 controls were analyzed for the PAI-1 -675 4G/5G polymorphism with diabetes risk, 7 studies with 1,060 cases and 1,139 controls for DN risk, 10 studies with 1,327 cases and 1,557 controls for DR and 4 studies with 610 cases and 1,042 controls for diabetic CAD risk respectively. Using allelic comparison (4G vs. 5G), the PAI-1 -675 4G/5G polymorphism was observed to have no significant association with diabetes (REM OR 1.07, 95% CI 0.96, 1.20), DN (REM OR 1.10, 95% CI 0.98, 1.25), DR (REM OR 1.09, 95% CI 0.97, 1.22) or diabetic CAD risk (REM OR 1.07, 95% CI 0.81, 1.42), and similar results were obtained in the dominant, recessive and co-dominant models. Our meta-analyses suggest that the PAI-1 -675 4G/5G polymorphism might not be a risk factor for DM, DN, DR or diabetic CAD risk in the populations investigated. This conclusion warrants confirmation by further studies.

摘要

进行了一项荟萃分析,以评估纤溶酶原激活物抑制剂-1(PAI-1)-675 4G/5G多态性与糖尿病(DM)、糖尿病肾病(DN)、糖尿病视网膜病变(DR)和糖尿病冠状动脉疾病(CAD)易感性之间的关联。通过基于文献的检索来识别所有相关研究。主要在等位基因水平计算固定效应或随机效应合并测量值,以确定研究之间的异质性偏倚。还进行了进一步的分层分析和敏感性分析。通过改良的Begg检验和Egger检验检查发表偏倚。荟萃分析纳入了20篇发表的文章,共27个结果:6项研究共1333例病例和3011例对照被分析PAI-1 -675 4G/5G多态性与糖尿病风险的关系,7项研究1060例病例和1139例对照分析DN风险,10项研究1327例病例和1557例对照分析DR风险,4项研究610例病例和1042例对照分析糖尿病CAD风险。采用等位基因比较(4G与5G),观察到PAI-1 -675 4G/5G多态性与糖尿病(随机效应比值比1.07,95%可信区间0.96,1.20)、DN(随机效应比值比1.10,95%可信区间0.98,1.25)、DR(随机效应比值比1.09,95%可信区间0.97,1.22)或糖尿病CAD风险(随机效应比值比1.07,95%可信区间0.81,1.42)均无显著关联,在显性、隐性和共显性模型中也得到了类似结果。我们的荟萃分析表明,在研究的人群中,PAI-1 -675 4G/5G多态性可能不是DM、DN、DR或糖尿病CAD风险的危险因素。这一结论有待进一步研究证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4fa/3818463/fcf55bf120c1/pone.0079150.g001.jpg

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