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SCGB3A2 多态性与格雷夫斯病风险的关联:一项荟萃分析。

The association of SCGB3A2 polymorphisms with the risk of Graves' disease: a meta-analysis.

机构信息

State Key Laboratory of Medical Genomics, Molecular Medical Centre, Shanghai Institute of Endocrinology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Endocrine. 2014 Apr;45(3):365-9. doi: 10.1007/s12020-013-0021-0. Epub 2013 Aug 10.

Abstract

The aim of this study is to assess the association of the SCGB3A2 -112G>A promoter polymorphism with Graves' disease(GD) using a meta-analysis. Relevant studies were identified using PubMed and EMBASE electronic databases. A meta-analysis of relevant studies was performed. This meta-analysis included four case-control studies, containing 6,913 GD cases (Caucasian 3904, Han 3009) and 7,185 controls(Caucasian 4155, Han 3030). The combined results showed a significant difference in genotype distribution (-112A/G) between GD and control populations (A vs. G P = 1.53 × 10(-7); GG vs. AA+AG P = 6.78 × 10(-9)). Meta-analysis was performed using a fixed-effects model. Under the dominant model (GG/AA + GA), the AA and GA genotypes were significantly associated with GD (pooled OR = 1.24, 95 % CI 1.12-1.37). When the two European studies are combined, the AA and GA genotypes were also significantly associated with GD (pooled OR = 1.29, 95 % CI 1.20-1.39). This meta-analysis suggests that SCGB3A2 polymorphism at positions -112G>A was associated with GD both in Chinese and Caucasian population.

摘要

本研究旨在通过荟萃分析评估 SCGB3A2-112G>A 启动子多态性与格雷夫斯病(GD)的相关性。使用 PubMed 和 EMBASE 电子数据库确定相关研究。对相关研究进行荟萃分析。这项荟萃分析包括四项病例对照研究,包含 6913 例 GD 病例(白种人 3904 例,汉族 3009 例)和 7185 例对照(白种人 4155 例,汉族 3030 例)。合并结果显示,GD 组和对照组之间基因型分布(-112A/G)存在显著差异(A 对 G,P=1.53×10(-7);GG 对 AA+AG,P=6.78×10(-9))。使用固定效应模型进行荟萃分析。在显性模型(GG/AA+GA)下,AA 和 GA 基因型与 GD 显著相关(合并 OR=1.24,95%CI 1.12-1.37)。当合并两项欧洲研究时,AA 和 GA 基因型也与 GD 显著相关(合并 OR=1.29,95%CI 1.20-1.39)。这项荟萃分析表明,SCGB3A2 基因在-112 位的 G/A 多态性与中国和白种人群的 GD 均有关。

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