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FCGR2A基因rs1801274位点基因多态性与川崎病相关性研究的Meta分析
作者:蒋勇  李敬风 
单位:湖北省十堰市太和医院 西安交通大学附属医院 儿科, 湖北 十堰 442000
关键词:rs1801274位点 基因多态性 川崎病 Meta分析 
分类号:R725.4
出版年·卷·期(页码):2017·36·第四期(465-471)
摘要:

目的:采用Meta分析的方法对FCGR2A基因rs1801274位点多态性与川崎病相关性研究进行分析。方法:截至2016年8月,计算机检索英文数据库(PubMed、EMbase)及中文数据库[中国知网(CNKI)、维普期刊资源整合服务平台(VIP)和万方数据知识服务平台(Wanfang)、中国生物医学文献服务系统(SinoMed)]中rs1801274位点基因多态性与川崎病相关性研究。采用Stata 12.0软件进行Meta分析。结果:共纳入8篇文献,包括3 724例患儿(川崎病组)和14 278例对照(对照组)。rs1801274位点基因多态性在等位基因模型(A vs G)、共显性模型(AG vs GG、AA vs GG)、显性模型(AG+AA vs GG)和隐性模型(AA vs AG+GG)比较模型下均与川崎病患病风险增加相关,合并OR值及其95%CI分别为1.387(1.299~1.480)、1.501(1.072~2.102)、1.959(1.403~2.735)、1.736(1.258~2.396)、1.397(1.174~1.661)。各研究异质性检验、Begg's检验和Egger's检验均P>0.1。结论:rs1801274位点基因多态性与川崎病相关,A等位基因是发生川崎病的危险基因。

Objective: To systematically evaluate the association between single nucleotide polymorphism of rs1801274 genetic susceptibility and Kawasaki disease(KD).Methods: The literature retrieval was conducted by using English databases(Medline, EMbase),Chinese databases(CNKI,Vip,Wanfang,SinaMed) and others to collect the published papers on the association between single nucleotide polymorphism of rs1801274 genetic susceptibility and KD by the end of June 2016. Meta-analysis was performed with software Stata 12.0. Results: Eight case-control studies were included in the final Meta-analysis, including a total of 3 724 KD patients and 14 278 controls.There were significant associations between increased risk of KD and single nucleotide polymorphism of rs1801274.the combined OR was 1.387(1.299-1.480) for A vs G, 1.501(1.072-2.102) for AG vs GG, 1.959(1.403-2.735) for AA vs GG,1.736(1.258-2.396) for AG+AA vs GG,1.397(1.174-1.661) for AA vs AG+GG.Each study heterogeneity test, Begg's inspection and Egger's inspection were all P>0.1. Conclusion: There is significant association between KD and single nucleotide polymorphism of rs1801274,and A allele is a high risk gene for KD.

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