Kidney Research Center, Tabriz University of Medical Sciences, Tabriz 5166615731, Iran.
Center of Experimental Orthopaedics, Saarland University Medical Center, D-66421 Homburg, Germany.
Nutrients. 2021 Mar 27;13(4):1101. doi: 10.3390/nu13041101.
Vitamin D deficiency has adverse effects on renal allograft outcomes, and polymorphisms of genes encoding vitamin D-binding protein (VDBP) and vitamin D receptor (VDR) are defined to play a role in these conditions. The goal of the current investigation was to evaluate the connection between those polymorphisms with acute rejection, viral infection history, and recipients' vitamin D status. In this study, 115 kidney transplant recipients and 100 healthy individuals were included. VDR polymorphisms including I (rs2228570), (rs7975232), (rs1544410), as well as VDBP (rs7040) polymorphisms were studied using high resolution melting (PCR-HRM) analysis among the studied groups. The frequency of G allele in rs7975232 polymorphism in the kidney transplant recipients was 0.63 times lower than healthy individuals ( = 0.026). Further, the G allele frequency in VDBP rs7040 polymorphism was significantly lower in patients with allograft rejection ( = 0.002). Considering the incidence of viral infection, significant differences were identified between the frequencies of VDR I (OR = 2.035; 95% CI 1.06-2.89, = 0.030) and VDBP rs7040 (OR = 0.40; 95% CI 0.24-0.67, < 0.001) T alleles in the studied groups. Moreover, the VDBP rs7040 GG genotype distribution was low in the recipients with a history of viral infection ( = 0.004). VDR (I) and VDBP (rs7040) alleles and their genotype distribution are significantly associated with allograft outcomes including allograft rejection and viral infection in the studied population.
维生素 D 缺乏对肾移植的结果有不良影响,编码维生素 D 结合蛋白 (VDBP) 和维生素 D 受体 (VDR) 的基因的多态性被定义为在这些情况下发挥作用。本研究旨在评估这些多态性与急性排斥反应、病毒感染史以及受者维生素 D 状态之间的关系。在这项研究中,纳入了 115 名肾移植受者和 100 名健康个体。使用高分辨率熔解(PCR-HRM)分析研究了 VDR 多态性,包括 I(rs2228570)、(rs7975232)、(rs1544410),以及 VDBP(rs7040)多态性。在肾移植受者中,rs7975232 多态性的 G 等位基因频率比健康个体低 0.63 倍(=0.026)。此外,在移植物排斥的患者中,VDBP rs7040 多态性的 G 等位基因频率显著降低(=0.002)。考虑到病毒感染的发生率,在 VDR I(OR=2.035;95%CI 1.06-2.89,=0.030)和 VDBP rs7040(OR=0.40;95%CI 0.24-0.67,<0.001)的等位基因频率在研究组之间存在显著差异。此外,在有病毒感染史的受者中,VDBP rs7040 GG 基因型分布较低(=0.004)。VDR(I)和 VDBP(rs7040)等位基因及其基因型分布与研究人群中的移植物排斥和病毒感染等移植物结果显著相关。