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CD40基因rs1883832多态性与格雷夫斯病风险的关联:一项荟萃分析。

Association between the CD40 rs1883832 polymorphism and Graves' disease risk: a meta-analysis.

作者信息

Wang Xiao-Xiong, Wang Xiao-Xia, Chen Tong

机构信息

Department of Ophthalmology, Beijing Hospital, National Center of Gerontology, Beijing, China.

Department of Endocrinology, Beijing Hospital, National Center of Gerontology, Beijing, China.

出版信息

EXCLI J. 2019 Jan 23;18:10-20. eCollection 2019.

Abstract

This meta-analysis aims to evaluate whether the rs1883832 polymorphism is associated with Graves' disease (GD) risk in different populations. We performed a systematic literature search in China National Knowledge Infrastructure (CNKI), Web of Science, and Pubmed databases to identify case-control association studies on the association between rs1883832 and GD risk. For each study we calculated the odds ratios (OR) and 95 % confidence intervals (CI) assuming dominant, recessive and homozygote models. We then calculated pooled ORs and 95 % CIs. After applying inclusion and exclusion criteria, 17 studies involving 4707 cases and 4215 controls were included in the meta-analysis. The results showed that rs1883832 was associated with GD risk in Asians under dominant (CT + TT vs CC, OR=0.67, 95 % CI: 0.56-0.81, P<0.001), recessive (TT vs CT + CC, OR=0.58, 95 % CI: 0.47-0.72, P<0.001), and homozygote (TT vs CC, OR=0.49, 95 % CI: 0.37-0.64, P<0.001) models. In Caucasians, rs1883832 was associated with GD risk under the dominant model (CT + TT vs CC, OR=0.82, 95 % CI: 0.68-0.99, P=0.042). Besides GD, we evaluated the relation of rs1883832 with Graves' ophthalmopathy (GO), finding that rs1883832 was associated with GO under the dominant model (CT + TT vs CC, OR=0.82, 95 % CI: 0.69-0.98, P=0.031). The findings of our meta-analysis suggest that the rs1883832 polymorphism is protective against GD and GO in Asians and Caucasians.

摘要

本荟萃分析旨在评估rs1883832多态性是否与不同人群的格雷夫斯病(GD)风险相关。我们在中国知网(CNKI)、科学网(Web of Science)和PubMed数据库中进行了系统的文献检索,以确定关于rs1883832与GD风险关联的病例对照研究。对于每项研究,我们在显性、隐性和纯合子模型下计算优势比(OR)和95%置信区间(CI)。然后计算合并的OR和95%CI。应用纳入和排除标准后,17项涉及4707例病例和4215例对照的研究被纳入荟萃分析。结果显示,在显性模型(CT + TT vs CC,OR = 0.67,95%CI:0.56 - 0.81,P < 0.001)、隐性模型(TT vs CT + CC,OR = 0.58,95%CI:0.47 - 0.72,P < 0.001)和纯合子模型(TT vs CC,OR = 0.49,95%CI:0.37 - 0.64,P < 0.001)下,rs1883832与亚洲人的GD风险相关。在白种人中,在显性模型下(CT + TT vs CC,OR = 0.82,95%CI:0.68 - 0.99,P = 0.042),rs1883832与GD风险相关。除了GD,我们还评估了rs1883832与格雷夫斯眼病(GO)的关系,发现在显性模型下(CT + TT vs CC,OR = 0.82,95%CI:0.69 - 0.98,P = 0.031),rs1883832与GO相关。我们荟萃分析的结果表明,rs1883832多态性对亚洲人和白种人的GD和GO具有保护作用。

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