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CTLA-4 基因多态性与类风湿关节炎易感性的关联:荟萃分析。

Polymorphisms in the CTLA-4 gene and rheumatoid arthritis susceptibility: a meta-analysis.

机构信息

The 452nd Military Hospital of China, Chengdu, Sichuan, 610041, China.

出版信息

J Clin Immunol. 2012 Jun;32(3):530-9. doi: 10.1007/s10875-012-9650-y. Epub 2012 Feb 23.

Abstract

INTRODUCTION

The +49A/G polymorphism and CT60 polymorphism in the CTLA-4 gene have been extensively examined for the association with rheumatoid arthritis (RA); however, results of different studies have been inconclusive. The aim of this study is to comprehensively evaluate the genetic risks of +49A/G and CT60 polymorphisms in the CTLA-4 gene for RA.

METHODS

A meta-analysis was carried out to analyze the association of +49A/G and CT60 polymorphisms with RA risk.

RESULTS

A total of 30 case-control studies in 20 articles were included in this meta-analysis. The results indicated that the variant G allele carriers (GG + GA) of +49A/G polymorphism had an 18% increased risk of RA when compared with the homozygote AA (odds ratio (OR) = 1.18, 95% confidence interval (CI): 1.04-1.34 for GG + AG vs. AA). In addition, the variant CT60 A allele carriers of CT60 polymorphism had a 14% decreased risk of RA when compared with the homozygote GG (OR = 0.86, 95%CI = 0.78-0.95 for AA + AG vs. GG). In the subgroup analysis by ethnicity, significant elevated RA risks were associated with +49G allele carriers in Asians, but not in Europeans. However, for CT60 polymorphism, significant decreased RA risks were associated with CT60 A allele carriers in Europeans, but not in Asians.

CONCLUSIONS

This meta-analysis suggested that the +49A/G and CT60 polymorphisms in the CTLA-4 gene may be risk factors for RA.

摘要

简介

CTLA-4 基因中的+49A/G 多态性和 CT60 多态性已被广泛研究与类风湿关节炎(RA)的相关性;然而,不同研究的结果并不一致。本研究旨在综合评估 CTLA-4 基因+49A/G 和 CT60 多态性的遗传风险与 RA。

方法

进行荟萃分析以分析+49A/G 和 CT60 多态性与 RA 风险的相关性。

结果

本荟萃分析共纳入 20 篇文章中的 30 项病例对照研究。结果表明,与 AA 纯合子相比,+49A/G 多态性的变异 G 等位基因携带者(GG+GA)患 RA 的风险增加 18%(比值比(OR)=1.18,95%置信区间(CI):1.04-1.34,GG+AG 与 AA 相比)。此外,与 GG 纯合子相比,CT60 多态性的变异 CT60 A 等位基因携带者患 RA 的风险降低 14%(OR=0.86,95%CI=0.78-0.95,AA+AG 与 GG 相比)。按种族亚组分析,+49G 等位基因携带者在亚洲人群中与 RA 风险显著升高相关,但在欧洲人群中则不相关。然而,对于 CT60 多态性,在欧洲人群中,CT60 A 等位基因携带者与 RA 风险显著降低相关,但在亚洲人群中则不相关。

结论

本荟萃分析提示 CTLA-4 基因中的+49A/G 和 CT60 多态性可能是 RA 的危险因素。

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