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Monocyte chemoattractant protein-1 promoter-2518 polymorphism and susceptibility to vasculitis, rheumatoid arthritis, and multiple sclerosis: A meta-analysis

机译:单核细胞趋化蛋白-1启动子2518多态性和易患血管炎,类风湿性关节炎和多发性硬化症的荟萃分析

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The purpose of this study was to examine whether the monocyte chemoattractant protein-1 (MCP-1) promoter -2518 A/G polymorphism (rs1024611) is associated with susceptibility to vasculitis, rheumatoid arthritis (RA), or multiple sclerosis (MS). A meta-analysis was conducted on the association between the MCP-1 -2518 A/G polymorphism and vasculitis, RA, and MS. Fourteen studies from 13 articles, including six on vasculitis, five on RA, and three on MS, consisting of 3,038 patients and 3,545 controls were available for the meta-analysis. The meta-analysis revealed no association between the MCP-1 -2518 G allele and vasculitis (odds ratio [OR] = 0.990, 95% confidence interval [CI] = 0.749-1.309, p = 0.943). Stratification by ethnicity indicated no association between the G allele of the MCP-1 -2518 A/G polymorphism and vasculitis in Asians and Caucasians. Meta-analysis by vasculitis type revealed an association between the GG+GA genotype of the MCP-1 -2518 A/G polymorphism and Beheet's disease (BD; OR = 1.349, 95% CI = 1.013-1.796, p = 0.040). However, sensitivity analysis showed that the association was not statistically significant after removing a study that was conducted in China (OR = 1.030, 95% CI = 0.667-1.590, p = 0.895), which indicated that the association was not statistically robust. The meta-analysis revealed no association between the MCP-1 -2518 G allele and RA (OR = 0.986, 95% CI = 0.890-1.093, p = 0.793) or MS (OR = 1.281, 95% CI = 0.802-2.046, p = 0.301). Our meta-analysis demonstrates that the MCP-1 -2518 A/G polymorphism is not associated with susceptibility to vasculitis, RA, or MS.
机译:这项研究的目的是检查单核细胞趋化蛋白-1(MCP-1)启动子-2518 A / G多态性(rs1024611)是否与血管炎,类风湿关节炎(RA)或多发性硬化症(MS)的易感性相关。对MCP-1 -2518 A / G多态性与血管炎,RA和MS之间的关联进行了荟萃分析。这项荟萃分析提供了来自13篇文章的14项研究,其中包括6篇关于血管炎的文章,5篇关于RA的文章和3篇关于MS的文章,包括3038名患者和3,545名对照。荟萃分析显示,MCP-1 -2518 G等位基因与血管炎之间无关联(优势比[OR] = 0.990,95%置信区间[CI] = 0.749-1.309,p = 0.943)。按种族分层表明,在亚洲人和高加索人中,MCP-1 -2518 A / G多态性的G等位基因与脉管炎之间没有关联。血管炎类型的荟萃分析显示,MCP-1 -2518 A / G多态性的GG + GA基因型与Beheet病之间存在关联(BD; OR = 1.349,95%CI = 1.013-1.796,p = 0.040)。但是,敏感性分析表明,删除在中国进行的一项研究后,该关联没有统计学意义(OR = 1.030,95%CI = 0.667-1.590,p = 0.895),这表明该关联在统计上并不稳健。荟萃分析显示MCP-1 -2518 G等位基因与RA(OR = 0.986,95%CI = 0.890-1.093,p = 0.793)或MS(OR = 1.281,95%CI = 0.802-2.046, p = 0.301)。我们的荟萃分析表明,MCP-1 -2518 A / G多态性与血管炎,RA或MS的易感性无关。

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