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Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort

机译:核受体基因多态性和华法林的魁北克华法林队列的剂量要求

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摘要

Warfarin is primarily metabolized by cytochrome 2C9, encoded by gene CYP2C9. Here, we investigated whether variants in nuclear receptor genes which regulate the expression of CYP2C9 are associated with warfarin response. We used data from 906 warfarin users from the Quebec Warfarin Cohort (QWC) and tested the association of warfarin dose requirement at 3 months following the initiation of therapy in nine nuclear receptor genes: NR1I3, NR1I2, NR3C1, ESR1, GATA4, RXRA, VDR, CEBPA, and HNF4A. Three correlated SNPs in the VDR gene (rs4760658, rs11168292, and rs11168293) were associated with dose requirements of warfarin (P = 2.68 x 10(-5), P = 5.81 x 10(-4), and P = 5.94 x 10(-4), respectively). Required doses of warfarin were the highest for homozygotes of the minor allele at the VDR variants (P < 0.0026). Variants in the VDR gene were associated with the variability in response to warfarin, emphasizing the possible clinical relevance of nuclear receptor gene variants on the inter-individual variability in drug metabolism.
机译:Warfarin主要由细胞色素2C9代谢,由基因CYP2C9编码。在这里,我们研究了调节CYP2C9表达的核受体基因中的变体是否与华法林应答有关。我们使用来自906华林用户的数据来自魁北克华法林队列(QWC),并在九个核受体基因疗法开始后3个月测试了Warfarin剂量要求的协会:NR1I3,NR1I2,NR3C1,ESR1,GATA4,RXRA,VDR ,CEBPA和HNF4A。 VDR基因中的三个相关的SNP(RS4760658,RS11168292和RS11168293)与Warfarin的剂量要求有关(P = 2.68×10(-5),P = 5.81 x 10(-4),P = 5.94 x 10( -4)分别)。需要剂量的Warfarin对于VDR变体的次次等位基因的纯合子是最高的(P <0.0026)。 VDR基因中的变体与响应华法林的可变性有关,强调核受体基因变异对药物代谢间间可变异性的可能临床相关性。

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