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首页> 外文期刊>DNA and Cell Biology >Correlations of MCP-1 -2518A > G Polymorphism and Serum Levels with Cerebral Infarction Risk: A Meta-Analysis
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Correlations of MCP-1 -2518A > G Polymorphism and Serum Levels with Cerebral Infarction Risk: A Meta-Analysis

机译:MCP-1 -2518A> G多态性和血清水平与脑梗死风险的相关性:荟萃分析

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This meta-analysis was performed to evaluate the relationships between the monocyte chemoattractant protein-1 (MCP-1) -2518A > G (rs1024611 A > G) polymorphism and its serum levels, and the risk of cerebral infarction. The PubMed, CISCOM, CINAHL, Web of Science, Google Scholar, EBSCO, Cochrane Library, and CBM databases were searched for relevant articles published before October 1st, 2013 without language restrictions. Meta-analysis was conducted using the STATA 12.0 software. Crude odds ratios (ORs) or standardized mean difference (SMD) with their 95% confidence intervals (95% CIs) were calculated. Twelve case-control studies that met all the inclusion criteria were included in this meta-analysis. A total of 1272 patients with cerebral infarction and 1210 healthy control subjects were involved in this meta-analysis. Our meta-analysis results reveal that the MCP-1 -2518A > G polymorphism might increase the risk of cerebral infarction (A allele vs. G allele: OR=1.37, 95% CI: 1.18-1.60, p 0.001; GA + AA vs. GG: OR=1.33, 95% CI: 1.09-1.62, p = 0.005; respectively). Furthermore, cerebral infarction patients had higher levels of serum MCP-1 than did healthy control subjects (SMD = 2.96, 95% CI: 2.00-3.92, p 0.001). Statistical analysis revealed no evidence of publication bias in this meta-analysis (all p > 0.05). Our findings indicate that the MCP-1 -2518A > G polymorphism and serum MCP-1 levels may contribute to the development of cerebral infarction. Thus, the MCP-1 -2518A > G polymorphism and serum MCP-1 levels could be potential biomarkers for the early detection of cerebral infarction.
机译:进行这项荟萃分析,以评估单核细胞趋化蛋白-1(MCP-1)-2518A> G(rs1024611 A> G)多态性与其血清水平和脑梗死风险之间的关系。在PubMed,CISCOM,CINAHL,Web of Science,Google Scholar,EBSCO,Cochrane图书馆和CBM数据库中搜索了2013年10月1日之前发布的相关文章,而没有语言限制。使用STATA 12.0软件进行荟萃分析。计算出具有95%置信区间(95%CI)的原油比值比(OR)或标准化均值差(SMD)。符合所有纳入标准的十二项病例对照研究被纳入该荟萃分析。这项荟萃分析共涉及1272例脑梗死患者和1210例健康对照者。我们的荟萃分析结果表明,MCP-1 -2518A> G多态性可能会增加脑梗死的风险(A等位基因与G等位基因:OR = 1.37,95%CI:1.18-1.60,p <0.001; GA + AA与GG:OR = 1.33,95%CI:1.09-1.62,p = 0.005;)。此外,脑梗死患者的血清MCP-1水平高于健康对照组(SMD = 2.96,95%CI:2.00-3.92,p <0.001)。统计分析显示,在该荟萃分析中没有证据显示出版物存在偏倚(所有p> 0.05)。我们的发现表明,MCP-1 -2518A> G多态性和血清MCP-1水平可能有助于脑梗死的发展。因此,MCP-1 -2518A> G多态性和血清MCP-1水平可能是早期发现脑梗死的潜在生物标志物。

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