Department of Nephrology, Nanjing Children's Hospital, Affiliated to Nanjing Medical University , Nanjing , China.
Ren Fail. 2013 Oct;35(9):1295-301. doi: 10.3109/0886022X.2013.820663. Epub 2013 Aug 1.
The association between angiotensin II type 1 receptor (AT1R) A 1166C (rs5186) gene polymorphism and end-stage renal disease (ESRD) risk remains controversial. We aimed to assess the association between AT1R A1166C gene polymorphism and ESRD susceptibility by performing a meta-analysis. Eligible studies were searched according to a predefined criterion using electronic databases. Eight articles were identified for the analysis of the association between AT1R A1166C gene polymorphism and ESRD risk. A allele and AA genotype were not associated with ESRD risk in overall populations, Caucasians and Asians (overall populations: p = 0.834 and 0.832, Caucasians: p = 0.853 and 0.884, Asians: p = 0.243 and 0.982). CC and AC genotype were not associated with ESRD risk in overall populations, Caucasians and Asians (overall populations: p = 0.304 and 0.712, Caucasians: p = 0.510 and 0.987, Asians: p = 0.319 and 0.225). In conclusion, AT1R A1166C gene polymorphism may not be correlated with ESRD risk in overall populations, Caucasians and Asians. However, more studies should be performed in the future.
血管紧张素 II 型 1 型受体 (AT1R) A1166C(rs5186) 基因多态性与终末期肾病 (ESRD) 风险之间的关联仍存在争议。我们旨在通过荟萃分析评估 AT1R A1166C 基因多态性与 ESRD 易感性之间的关系。根据预先确定的标准,使用电子数据库搜索符合条件的研究。确定了 8 篇文章来分析 AT1R A1166C 基因多态性与 ESRD 风险之间的关联。在总体人群、白人和亚洲人中,A 等位基因和 AA 基因型与 ESRD 风险无关(总体人群:p=0.834 和 0.832,白种人:p=0.853 和 0.884,亚洲人:p=0.243 和 0.982)。在总体人群、白人和亚洲人中,CC 和 AC 基因型与 ESRD 风险无关(总体人群:p=0.304 和 0.712,白种人:p=0.510 和 0.987,亚洲人:p=0.319 和 0.225)。总之,AT1R A1166C 基因多态性与总体人群、白人和亚洲人群的 ESRD 风险无关。然而,未来需要进行更多的研究。