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IFIH1 rs1990760 多态性与自身免疫性疾病易感性的关联:荟萃分析。

Association of IFIH1 rs1990760 polymorphism with susceptibility to autoimmune diseases: a meta-analysis.

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University , 81 Meishan Road, Hefei, Anhui , PR China .

出版信息

Autoimmunity. 2013 Nov;46(7):455-62. doi: 10.3109/08916934.2013.796937. Epub 2013 Jun 4.

Abstract

Published data on the association between the IFIH1 rs1990760 polymorphism and multiple autoimmune diseases are controversial and inconclusive. To more precisely estimate the association between the IFIH1 rs1990760 polymorphism and susceptibility to autoimmune diseases, a meta-analysis was conducted. Studies examining the association of the IFIH1 rs1990760 polymorphism with autoimmune diseases were exhaustively searched using PubMed, Web of Science and a review of the references. A total of 19 studies with 26 comparisons including 8 type 1 diabetes (T1D), 5 systemic lupus erythematosus (SLE), 5 Graves' disease (GD), 2 multiple sclerosis (MS), 2 rheumatoid arthritis (RA), 2 Hashimoto's thyroiditis (HT), 2 autoimmune Addison's disease (AAD) were available for this meta-analysis. Meta-analysis was performed for genotype T/T + T/C (dominant model), genotype T/T (recessive model) and T-allele in fixed or random-effects models. The overall odds ratios (ORs) and 95% confidence intervals (CIs) for T-allele were T1D (OR = 1.184, 95% CI = 1.142-1.229), SLE (OR = 1.143, 95% CI = 1.073-1.217), MS (OR = 1.181, 95% CI = 1.062-1.313) and RA (OR = 1.115, 95% CI = 1.004-1.239), respectively. For T1D and SLE, significant association was observed in the population of European ancestry, but not in the Asian population. This meta-analysis demonstrates that the IFIH1 rs1990760 T-allele confers susceptibility to T1D, SLE, MS and RA and suggests that the IFIH1 rs1990760 polymorphism might have no effect on GD and AAD. Our result provides further evidence for the notion of common gene underlying multiple autoimmune diseases.

摘要

已发表的关于 IFIH1 rs1990760 多态性与多种自身免疫性疾病之间关联的数据存在争议且尚无定论。为了更准确地评估 IFIH1 rs1990760 多态性与自身免疫性疾病易感性之间的关联,进行了荟萃分析。使用 PubMed、Web of Science 和文献综述,全面搜索了研究 IFIH1 rs1990760 多态性与自身免疫性疾病关联的研究。这项荟萃分析共纳入了 19 项研究,包括 8 项 1 型糖尿病(T1D)、5 项系统性红斑狼疮(SLE)、5 项格雷夫斯病(GD)、2 项多发性硬化症(MS)、2 项类风湿关节炎(RA)、2 项桥本甲状腺炎(HT)和 2 项自身免疫性艾迪生病(AAD),共涉及 26 个比较。采用固定或随机效应模型,对基因型 T/T+T/C(显性模型)、基因型 T/T(隐性模型)和 T 等位基因进行荟萃分析。T 等位基因的总比值比(OR)和 95%置信区间(CI)为 T1D(OR=1.184,95%CI=1.142-1.229)、SLE(OR=1.143,95%CI=1.073-1.217)、MS(OR=1.181,95%CI=1.062-1.313)和 RA(OR=1.115,95%CI=1.004-1.239)。对于 T1D 和 SLE,在欧洲血统人群中观察到显著关联,但在亚洲人群中没有观察到关联。这项荟萃分析表明,IFIH1 rs1990760 T 等位基因易患 T1D、SLE、MS 和 RA,并提示 IFIH1 rs1990760 多态性可能对 GD 和 AAD 没有影响。我们的结果为多种自身免疫性疾病存在共同基因的观点提供了进一步的证据。

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