Li Li, Wan Qingsong, Yang Shikun, Zhao Saili
Department of Medicine, Hunan Environment-Biological Polytechnic, Hengyang, China.
Department of Nephrology, The First Affiliated Hospital of the University of South China, Hengyang, China.
Ther Apher Dial. 2018 Dec;22(6):575-587. doi: 10.1111/1744-9987.12714. Epub 2018 Jul 30.
Our pooled analysis aimed to assess the impact of vitamin D receptor (VDR) gene polymorphism on chronic renal failure (CRF) susceptibility. Relevant studies were searched from multiple databases, then pooled-analyses were performed using Stata software. Eighteen studies involving 2512 CRF patients and 3630 healthy controls were included. Pooled analysis showed that VDR ApaI and TaqI gene polymorphism were not associated with CRF susceptibility either in Asian or in Caucasians populations, and VDR BsmI and FokI gene polymorphism were not associated with CRF susceptibility in overall populations. The subgroup analysis showed that VDR BsmI gene polymorphism was associated with CRF susceptibility in Chinese under the Allele model (OR = 0.76, 95% CI: 0.59-0.97, P = 0.029). In Spanish individuals, VDR BsmI gene polymorphism was associated with CRF: Recessive model (BB vs. Bb + bb): OR = 1.60, 95% CI: 1.09-2.35, P = 0.016; Additive model (BB + bb vs. Bb): OR = 1.60, 95% CI: 1.21-2.12, P = 0.001). In addition, in the Asian subgroup, VDR FokI gene polymorphism was associated with CRF risk: Allele model (F vs. f): OR = 0.31, 95% CI: 0.16-0.59, P = 0.000; Dominant model (FF + Ff vs. ff): OR = 0.12, 95% CI: 0.03-0.59, P = 0.009 and Recessive model (FF vs. Ff + ff): OR = 0.32, 95% CI: 0.13-0.75, P = 0.009. This pooled analysis showed that VDR BsmI gene polymorphism was associated with CRF risk in the Chinese and Spanish individuals, and, VDR FokI gene polymorphism was associated with CRF risk in Asian subjects. But VDR ApaI and TaqI gene polymorphism were not associated with CRF risk either in Asian or in Caucasian individuals.
我们的汇总分析旨在评估维生素D受体(VDR)基因多态性对慢性肾衰竭(CRF)易感性的影响。从多个数据库检索相关研究,然后使用Stata软件进行汇总分析。纳入了18项研究,涉及2512例CRF患者和3630例健康对照。汇总分析表明,VDR ApaI和TaqI基因多态性在亚洲人群和白种人群中均与CRF易感性无关,VDR BsmI和FokI基因多态性在总体人群中与CRF易感性无关。亚组分析表明,在等位基因模型下,VDR BsmI基因多态性与中国人群的CRF易感性相关(OR = 0.76,95% CI:0.59 - 0.97,P = 0.029)。在西班牙人群中,VDR BsmI基因多态性与CRF相关:隐性模型(BB vs. Bb + bb):OR = 1.60,95% CI:1.09 - 2.35,P = 0.016;加性模型(BB + bb vs. Bb):OR = 1.60,95% CI:1.21 - 2.12,P = 0.001。此外,在亚洲亚组中,VDR FokI基因多态性与CRF风险相关:等位基因模型(F vs. f):OR = 0.31,95% CI:0.16 - 0.59,P = 0.000;显性模型(FF + Ff vs. ff):OR = 0.12,95% CI:0.03 - 0.59,P = 0.009;隐性模型(FF vs. Ff + ff):OR = 0.32,95% CI:0.13 - )。该汇总分析表明,VDR BsmI基因多态性与中国和西班牙人群的CRF风险相关,VDR FokI基因多态性与亚洲人群的CRF风险相关。但VDR ApaI和TaqI基因多态性在亚洲或白种人群中均与CRF风险无关。