Association between CTLA-4 gene polymorphism and risk of rheumatoid arthritis: a meta-analysis.

Association between CTLA-4 gene polymorphism and risk of rheumatoid arthritis: a meta-analysis.
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CTLA-4基因多态性与类风湿性关节炎风险之间的关联:荟萃分析

DOI:
10.18632/aging.203349
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发表时间:
2021-08-02
期刊:
Aging
影响因子:
--
通讯作者:
Liu H
Liu H
中科院分区:
其他
文献类型:
--
作者:
Zhou C;Gao S;Yuan X;Shu Z;Li S;Sun X;Xiao J;Liu H

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细胞毒性T淋巴细胞相关蛋白4 (CTLA-4)基因多态性可能参与类风湿关节炎(RA)的风险。然而,这种关联的证据仍然存在争议。因此,我们进行了荟萃分析,以确认CTLA-4基因多态性与RA之间的关系。计算合并优势比(or)和95%置信区间(ci)来评估关联强度。按种族进行分层分析。共获得66项病例对照研究,其中病例21681例,对照23457例。rs3087243多态性在亚洲人(A vs. G: OR=0.77, 95%CI=0.65 ~ 0.90, P=0.001; AA vs. GG: OR=0.67, 95%CI=0.48 ~ 0.94, P=0.02)和高加索人(A vs. G: OR=0.89, 95%CI=0.86 ~ 0.93, P<0.00001; AA vs. GG: OR=0.81, 95%CI=0.75 ~ 0.88, P<0.00001)中检测到显著关联。rs231775多态性在总体(G vs. A: OR= 1.16, 95%CI=1.08-1.25, P<0.0001; GG vs. AA: OR=1.29, 95%CI=1.12-1.50, P=0.0006)和亚洲人(G vs. A: OR=1.27, 95%CI=1.10-1.47, P=0.001; GG vs. AA: OR=1.58, 95%CI=1.24-2.01, P=0.0002)中观察到显著相关性,但在白种人中无显著相关性。然而,rs5742909多态性与RA之间没有关联。该荟萃分析证实rs3087243和rs231775多态性在总体人群和种族特异性分析中与RA风险相关,但rss5742909多态性与RA风险无关。
Cytotoxic T lymphocyte-associated protein 4 (CTLA-4) gene polymorphisms may be involved in the risk of Rheumatoid arthritis (RA). However, evidence for the association remains controversial. Therefore, we performed a meta-analysis to confirm the relationship between CTLA-4 gene polymorphisms and RA. The pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the strength of association. Stratified analysis was conducted by ethnicity. In total, 66 case-control studies including 21681 cases and 23457 controls were obtained. For rs3087243 polymorphism, significant association was detected in Asians (A vs. G: OR=0.77, 95%CI=0.65-0.90, P=0.001; AA vs. GG: OR=0.67, 95%CI=0.48-0.94, P=0.02) and Caucasians (A vs. G: OR=0.89, 95%CI=0.86-0.93, P<0.00001; AA vs. GG: OR=0.81, 95%CI=0.75-0.88, P<0.00001). For rs231775 polymorphism, significant association was observed in the overall (G vs. A: OR =1.16, 95%CI=1.08-1.25, P<0.0001; GG vs. AA: OR=1.29, 95%CI=1.12-1.50, P=0.0006), and in Asians (G vs. A: OR=1.27, 95%CI=1.10-1.47, P=0.001; GG vs. AA: OR=1.58, 95%CI=1.24-2.01, P=0.0002), but not in Caucasians. However, there was no association between rs5742909 polymorphism and RA. This meta-analysis confirmed that rs3087243 and rs231775 polymorphism were associated with the risk of RA in both overall population and ethnic-specific analysis, but there was no association between rs5742909 polymorphism and RA risk.
DOI: 10.1016/j.gene.2014.12.046
发表时间: 2015-03-01
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