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The Correlation between E-Selectin S128R Gene Polymorphism and Ischemic Stroke in Chinese Population : A Meta-Analysis

机译:e-Selectin S128R基因多态性与中国人群中缺血性卒中之间的相关性:Meta分析

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摘要

To perform a systematic review of the data collected from case-control studies conducted earlier to investigate the correlation between E-selectin S128R polymorphism and ischemic stroke (IS) risk among the Chinese population. The PubMed, Web of Science, Chinese biomedical literature database (CBM), Chinese databases China National Knowledge Infrastructure (CNKI), WanfangData knowledge service platform (Wanfang Data), and information resource integration service platform (VIP) Databases were searched to retrieve case-control studies on the correlation between E-selectin gene S128R polymorphism and IS from the inception of the database till June 2019. The literature was screened, data were extracted, the risk of bias was reviewed, and the studies included were assessed independently by two reviewers. Stata ver. 12.0 software (Stata Corp LLC, College Station, TX, USA) was used to perform the meta-analysis. A total of 2907 cases from eight case-control studies involving 1478 IS patients and 1429 controls were included in this study. The R allele and RS genotype in E-selectin were found to be associated with the risk of IS as per the results of the meta-analysis (R vs. S : odds ratio [OR], 2.75; 95% confidence interval [CI], 2.15–3.51; p<0.00001; RS vs. SS : OR, 2.50; 95% CI, 1.95–3.19; p<0.00001; RR+RS vs. SS : OR, 2.85, 95% CI, 2.21–3.67; p<0.00001). The E-selectin gene S128R polymorphism is likely related to IS based on the results of a meta-analysis in the Chinese population, and the R allele and RS genotype of E-selectin may be IS risk factors.
机译:为了对从之前进行的病例对照研究所收集的数据进行系统审查,以研究中国人群中e-Selectin S128R多态性和缺血性卒中(IS)风险之间的相关性的相关性。搜索中文数据库中国国家知识基础设施(CNKI),WANFANGDATA知识服务平台(WANFANG数据)和信息资源集成服务平台(VIP)数据库进行了PUBMED,中国生物医学文献数据库(CNKI),以及信息资源集成服务平台(VIP)数据库,以检索案例 - 对e-Selectin基因S128R多态性相关性的对照研究与数据库的初始化到2019年6月。提取了文献,提取了数据,审查了偏见的风险,由两名审稿人独立评估了所附的研究。 stata ver。 12.0软件(Stata Corp LLC,College Station,TX,USA)用于执行Meta分析。共有2907例涉及1478项涉及的八种病例对照研究是患者,本研究纳入1429例。发现e-Selectin中的R等位基因和RS基因型与META分析结果的风险有关(R对S:差异[或],2.75; 95%置信区间[CI] ,2.15-3.51; p <0.00001; rs与ss:或2.50; 95%ci,1.95-3.19; p <0.00001; rr + rs与ss:,或,2.85,95%ci,2.21-3.67; p <0.00001)。 E-Selectin Gene S128R多态性可能是有关的,基于中国人群中的荟萃分析的结果,e-Selectin的R等位基因和RS基因型可能是危险因素。

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