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单核细胞趋化蛋白-1启动子-2518多态性与血管炎、类风湿关节炎及多发性硬化易感性的荟萃分析。

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

作者信息

Lee Y H, Bae S-C

机构信息

Korea University College of Medicine Division of Rheumatology, Department of Internal Medicine Seoul Republic of Korea

Hanyang University Hospital for Rheumatic Diseases Department of Rheumatology Seoul Republic of Korea.

出版信息

Cell Mol Biol (Noisy-le-grand). 2016 Mar 20;62(3):65-71.

Abstract

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 Behçet'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.

摘要

本研究旨在探讨单核细胞趋化蛋白-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。从13篇文章中获取了14项研究,其中包括6项关于血管炎的研究、5项关于RA的研究和3项关于MS的研究,共有3038例患者和3545例对照可用于荟萃分析。荟萃分析显示,MCP-1 -2518 G等位基因与血管炎之间无关联(比值比[OR]=0.990,95%置信区间[CI]=0.749-1.309,p=0.943)。按种族分层表明,MCP-1 -2518 A/G多态性的G等位基因与亚洲人和高加索人的血管炎之间无关联。按血管炎类型进行的荟萃分析显示,MCP-1 -2518 A/G多态性的GG+GA基因型与白塞病(BD)之间存在关联(OR=1.349,95%CI=1.013-1.796,p=0.040)。然而,敏感性分析表明,在剔除一项在中国进行的研究后,该关联无统计学意义(OR=1.030,95%CI=0.667-1.590,p=0.895),这表明该关联在统计学上不稳健。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)之间无关联。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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