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山东大学学报(医学版) ›› 2017, Vol. 55 ›› Issue (5): 95-102.doi: 10.6040/j.issn.1671-7554.0.2016.1196

• 临床医学 • 上一篇    下一篇

STAT4 rs7574865位点单核苷酸多态性与系统性红斑狼疮易感性Meta分析

杜金阁1,陈慧2,杨孝荣1,吕明1,2   

  1. 1.山东大学公共卫生学院流行病学系, 山东 济南 250012;2.山东大学齐鲁医院科研处临床流行病学研究室, 山东 济南 250012
  • 收稿日期:2016-09-23 出版日期:2017-05-10 发布日期:2017-05-10
  • 通讯作者: 吕明. E-mail:lvming@sdu.edu.cn E-mail:lvming@sdu.edu.cn

Meta-analysis of the association between the STAT4 rs7574865 polymorphism and systemic lupus erythematosus

DU Jinge1, CHEN Hui2, YANG Xiaorong1, LÜ Ming1,2   

  1. 1. Department of Epidemiology, School of Public Health, Shandong University, Jinan 250012, Shandong, China;
    2. Clinical Epidemiology Unit, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Received:2016-09-23 Online:2017-05-10 Published:2017-05-10

摘要: 目的 通过Meta分析探讨信号转导和转录激活因子4(STAT4)基因rs7574865位点单核苷酸多态性(SNP)与系统性红斑狼疮(SLE)易感性之间的关系。 方法 两名研究者分别检索PubMed、Web of science、Scopus、中国知网和万方数据库,筛选出相关文献。用合并OR值和95% CI评价STAT4 rs7574865位点SNP与SLE易感性之间的关系。 结果 共纳入27篇研究,包含21 902例SLE患者和37 780例对照。Meta分析结果如下:等位基因模型(T vs G, OR=1.56, 95% CI:1.49~1.63),纯合子模型(TT vs GG, OR=2.32, 95% CI:2.08~2.58),杂合子模型(TG vs GG, OR=1.52, 95% CI:1.41~1.64),显性遗传模型(TT/TG vs GG, OR=1.67, 95% CI:1.55~1.79),隐性遗传模型(TT vs TG/GG, OR=1.83, 95% CI:1.65~2.02)。按研究对象所在的地区进行亚组分析后显示,所有亚组中,rs7574865 SNP均与SLE易感性有关。 结论 STAT4 rs7574865位点SNP与SLE的易感性有关,T等位基因的存在增加SLE的患病风险。

关键词: 系统性红斑狼疮, STAT4, 基因多态性, 单核苷酸多态性, Meta分析

Abstract: Objective To assess the association between STAT4 rs7574865 single nucleotide polymorphism and systemic lupus erythematosus by a Meta-analysis. Methods Two authors searched PubMed, Web of science, Scopus, China National Knowledge Infrastructure(CNKI)and Wanfang databases to identify relevant studies, independently. Odds ratio(OR)with 95% confidence interval(CI)were calculated to assess the strength of the association between rs7574865 polymorphism and SLE risk. Results A total of 27 studies were eventually included in this meta-analysis, which contained 21 902 SLE cases and 37 780 controls. Pooled analyses showed significant association between STAT4 rs7574865 polymorphism and SLE risk using allelic model(T vs G, OR=1.56, 95% CI: 1.49-1.63), homozygote model(TT vs GG, OR=2.32, 95% CI: 2.08-2.58), heterozygote model(TG vs GG, OR=1.52, 95% CI: 1.41-1.64), dominant model(TT/TG vs GG, OR=1.67, 95% CI: 1.55-1.79)and recessive model(TT vs TG/GG, OR=1.83, 95% CI: 1.65-2.02). In the subgroup analysis by region, evidences also showed significant association between rs7574865 polymorphism and SLE risk in all regions. Conclusion STAT4 rs7574865 G>T polymorphism correlate with an increased risk of SLE and the T allele may be a risk factor.

Key words: STAT4, Gene polymorphism, Single nucleotide polymorphism, Meta-analysis, Systemic lupus erythematosus

中图分类号: 

  • R181.3
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