Mao Song, Ren Xianguo, Huang Songming, Zhang Aihua
Department of Nephrology, Nanjing Children's Hospital, Affiliated to Nanjing Medical University , Nanjing , China and.
Ren Fail. 2014 Jun;36(5):817-22. doi: 10.3109/0886022X.2014.890058. Epub 2014 Feb 27.
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.
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。