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Lack of an association between vitamin D receptor bsmi gene polymorphism and the risk of end-stage renal disease: A meta-analysis

机译:维生素D受体bsmi基因多态性与终末期肾脏疾病风险之间缺乏关联的荟萃分析

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Objective To evaluate the association between vitamin D receptor (VDR) BsmI gene polymorphism and the risk of end-stage renal disease (ESRD). Methods All eligible studies were included in our meta-analysis of a search of the PubMed, Embase, Cochrane and China National Knowledge Infrastructure (CNKI) databases according to predefined criteria. The fixed-effects or, in the presence of heterogeneity, random-effects models were used to calculate the pooled odds ratio (OR) and corresponding 95% confidence interval (CI). Materials Six studies including 863 patients and 1,063 controls were recruited for the analysis of the association between the VDR BsmI gene polymorphism and the risk of ESRD. Results The B allele/BB genotype was not associated with the ESRD risk in the overall population, Caucasians or Asians (overall population: p=0.492 and 0.382, Caucasians: p=0.765 and 0.522, Asians: p=0.607 and 0.481). The Bb/bb genotype was also not associated with the risk of ESRD in the overall population, Caucasians or Asians (overall population: p=0.556 and 0.166, Caucasians: p=0.770 and 0.965, Asians: p=0.411 and 0.098). The exclusion of any single study had little impact on the p value in the overall population. No evidence of publication bias was observed. Conclusion VDR BsmI gene polymorphism appears to not be associated with the risk of ESRD in the overall population, Caucasians or Asians. However, more studies should be performed in the future.
机译:目的探讨维生素D受体(VDR)BsmI基因多态性与终末期肾脏疾病(ESRD)风险的关系。方法所有符合条件的研究均纳入我们根据既定标准对PubMed,Embase,Cochrane和中国国家知识基础设施(CNKI)数据库进行搜索的荟萃分析中。使用固定效应或存在异质性的随机效应模型来计算合并比值比(OR)和相应的95%置信区间(CI)。材料招募了包括863名患者和1,063名对照的六项研究,以分析VDR BsmI基因多态性与ESRD风险之间的关联。结果B等位基因/ BB基因型与总人群,白种人或亚洲人的ESRD风险无关(总人群:p = 0.492和0.382,白种人:p = 0.765和0.522,亚洲人:p​​ = 0.607和0.481)。 Bb / bb基因型也与总人口,白种人或亚洲人的ESRD风险无关(总人口:p = 0.556和0.166,白种人:p = 0.770和0.965,亚洲人:p​​ = 0.411和0.098)。排除任何一项研究对总体人群的p值影响很小。没有观察到发表偏见的证据。结论VDR BsmI基因多态性似乎与总体人群,白种人或亚洲人的ESRD风险无关。但是,将来应该进行更多的研究。

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