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首页> 外文期刊>Molecular biology reports >Associations between interleukin-23 receptor polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis
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Associations between interleukin-23 receptor polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis

机译:白介素23受体多态性与类风湿关节炎易感性的关联:一项荟萃分析

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The aim of this study was to determine whether interleukin-23 receptor (IL-23R) polymorphisms confer susceptibility to rheumatoid arthritis (RA). A meta-analysis was conducted on the associations between the IL-23R rs1343151, rs10489629, rs7517847, rs11209026, rs1004819, and rs2201841 polymorphisms and RA using (1) allele contrast, (2) the recessive model, (3) the dominant model, and (4) the additive model. A total of 13 studies from eight articles involving 10,016 RA patients and 11,967 controls were considered in the meta-analysis. Meta-analysis identified a significant association between RA and the A allele of the rs1343151 polymorphism in the overall population (OR = 1.110, 95 % CI = 1.056–1.168, p = 4.7 × 106). Stratification by ethnicity identified a significant association between this polymorphism and RA in Europeans (OR = 1.105, 95 % CI = 1.049–1.163, p = 1.4 × 105). An association was also found between RA and the A allele carrier of the rs1343151 polymorphism in Europeans (OR = 1.135, 95 % CI = 1.058–1.217, p = 4.0 × 105). Meta-analysis revealed a significant association between RA and the A allele of the rs10489629 polymorphism in the overall population (OR = 1.079, 95 % CI = 1.029–1.131, p = 0.002) and in Europeans (OR = 1.092, 95 % CI = 1.038–1.149, p = 0.001). Meta-analyses of recessive, dominant, and additive models showed the same pattern as the meta-analysis of the A allele of the rs10489629 polymorphism, that is, a significant association with RA in Europeans. However, no association was found between the IL-23R rs7517847, rs11209026, rs1004819, and rs2201841 polymorphisms and RA susceptibility. This meta-analysis shows that the IL-23R rs1343151 and rs10489629 polymorphisms are associated with the development of RA in Europeans. These findings suggest that the IL-23R genes confer susceptibility to RA in the European population, but further study of this association is required in other ethnic groups.
机译:这项研究的目的是确定白介素23受体(IL-23R)多态性是否赋予类风湿关节炎(RA)敏感性。使用(1)等位基因对比,(2)隐性模型,(3)优势模型,IL-23R rs1343151,rs10489629,rs7517847,rs11209026,rs1004819和rs2201841多态性与RA之间的关联进行了荟萃分析。 (4)加性模型。荟萃分析考虑了来自八篇文章的总共13项研究,涉及10016名RA患者和11967名对照。荟萃分析确定了RA与rs1343151多态性的A等位基因在总人群中存在显着相关性(OR = 1.110,95%CI = 1.056–1.168,p = 4.7×106)。通过种族分层确定了欧洲人这种多态性与RA之间的显着关联(OR = 1.105,95%CI = 1.049–1.163,p = 1.4×105)。在欧洲人中,RA与rs1343151多态性的A等位基因携带者之间也存在关联(OR = 1.135,95%CI = 1.058–1.217,p = 4.0×105)。荟萃分析显示,RA与rs10489629多态性的A等位基因在总人群中(OR = 1.079,95%CI = 1.029-1.131,p = 0.002)和在欧洲人中(OR = 1.092,95%CI = 1.038–1.149,p = 0.001)。隐性,显性和加性模型的荟萃分析显示出与rs10489629多态性的A等位基因的荟萃分析相同的模式,即与欧洲人的RA显着相关。但是,在IL-23R rs7517847,rs11209026,rs1004819和rs2201841多态性与RA敏感性之间未发现关联。这项荟萃分析表明,IL-23R rs1343151和rs10489629多态性与欧洲人RA的发展有关。这些发现表明,IL-23R基因在欧洲人群中对RA易感,但在其他种族中还需要进一步研究这种关联。

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