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Megsin基因2093C/T、2180C/T及C25663G多态性与IgA肾病风险的关联

Association of megsin 2093C/T, 2180C/T and C25663G gene polymorphism with the risk of IgA nephropathy.

作者信息

Mao Song, Ren Xianguo, Huang Songming, Zhang Aihua

机构信息

Department of Nephrology, Nanjing Children's Hospital, Affiliated to Nanjing Medical University , Nanjing , China and.

出版信息

Ren Fail. 2014 Jun;36(5):817-22. doi: 10.3109/0886022X.2014.890058. Epub 2014 Feb 27.

Abstract

The association between megsin 2093C/T, 2180C/T and C25663G gene polymorphisms and IgA nephropathy (IgAN) risk remains unclear. We aimed to evaluate the association between megsin 2093C/T, 2180C/T and C25663G gene polymorphisms and IgAN risk by performing a meta-analysis. Eligible studies were searched according to predefined criteria by using electronic databases. Six articles were identified for the analysis of the association between megsin 2093C/T, 2180C/T and C25663G gene polymorphisms and IgAN risk. 2093C/T C allele was associated with IgAN risk in overall populations and Asians (overall populations: p = 0.014, Asians: p = 0.037). 2093C/T CC/TT genotype was not associated with IgAN risk in overall populations, Caucasians and Asians. 2180C/T C allele was correlated with IgAN risk in Caucasians (p = 0.024). 2180C/T CC/TT genotype was not associated with IgAN risk in overall populations, Caucasians and Asians. C25663G gene polymorphism was not associated with IgAN onset in Asians. In conclusion, megsin 2093C/T C allele may be genetic marker for IgAN susceptibility in overall populations and Asians. 2180C/T C allele may be risk factor for IgAN onset in Caucasians. However, more studies should be performed in the future.

摘要

Megsin基因2093C/T、2180C/T和C25663G基因多态性与IgA肾病(IgAN)风险之间的关联尚不清楚。我们旨在通过进行荟萃分析来评估Megsin基因2093C/T、2180C/T和C25663G基因多态性与IgAN风险之间的关联。根据预定义标准使用电子数据库检索符合条件的研究。共纳入6篇文章分析Megsin基因2093C/T、2180C/T和C25663G基因多态性与IgAN风险之间的关联。2093C/T的C等位基因与总体人群和亚洲人群的IgAN风险相关(总体人群:p = 0.014,亚洲人群:p = 0.037)。2093C/T的CC/TT基因型与总体人群、白种人和亚洲人群的IgAN风险无关。2180C/T的C等位基因与白种人的IgAN风险相关(p = 0.024)。2180C/T的CC/TT基因型与总体人群、白种人和亚洲人群的IgAN风险无关。C25663G基因多态性与亚洲人群的IgAN发病无关。总之,Megsin基因2093C/T的C等位基因可能是总体人群和亚洲人群IgAN易感性的遗传标志物。2180C/T的C等位基因可能是白种人IgAN发病的危险因素。然而,未来需要进行更多的研究。

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