Wang Xiao-Xiong, Wang Xiao-Xia, Chen Tong
Department of Ophthalmology, Beijing Hospital, National Center of Gerontology, Beijing, China.
Department of Endocrinology, Beijing Hospital, National Center of Gerontology, Beijing, China.
EXCLI J. 2019 Jan 23;18:10-20. eCollection 2019.
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.
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。