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Genetic Variation of VKORC1 and CYP4F2 Genes Related to Warfarin Maintenance Dose in Patients with Myocardial Infarction

机译:心肌梗死患者中与华法林维持剂量有关的VKORC1和CYP4F2基因的遗传变异

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The aim of this study was to investigate whether the VKORC1*3 (rs7294/9041 G > A), VKORC1*4 (rs17708472/6009 C > T), and CYP4F2 (rs2108622/1347 C > T) polymorphisms were associated with elevated warfarin maintenance dose requirements in patients with myocardial infarction (n=105) from the Warfarin Aspirin Reinfarction Study (WARIS-II). We found significant associations between elevated warfarin dose requirements and VKORC1*3 and VKORC1*4 polymorphisms (P=.001andP=.004, resp.), whereas CYP4F2 (1347 C > T) showed a weak association on higher warfarin dose requirements (P=.09). However, analysing these variant alleles in a regression analysis together with our previously reported data on VKORC1*2, CYP2C9*2 and CYP2C9*3 polymorphisms, gave no significant associations for neither VKORC1*3, VKORC1*4 nor CYP4F2 (1347 C > T). In conclusion, in patients with myocardial infarction, the individual contribution to warfarin dose requirements from VKORC1*3, VKORC1*4, and CYP4F2 (1347 C > T) polymorphisms was negligible. Our results indicate that pharmacogenetic testing for VKORC1*2, CYP2C9*2 and CYP2C9*3 is more informative regarding warfarin dose requirements than testing for VKORC1*3, VKORC1*4, and CYP4F2 (1347 C > T) polymorphisms.
机译:这项研究的目的是调查VKORC1 * 3(rs7294 / 9041 G> A),VKORC1 * 4(rs17708472 / 6009 C> T)和CYP4F2(rs2108622 / 1347 C> T)多态性是否与华法林升高有关华法林阿司匹林再梗塞研究(WARIS-II)对心肌梗死患者(n = 105)维持剂量的要求。我们发现升高的华法林剂量要求与VKORC1 * 3和VKORC1 * 4多态性之间存在显着关联(P = .001和P = .004,分别),而CYP4F2(1347 C> T)与较高的华法林剂量要求之间存在弱关联(P = .09)。但是,在回归分析中分析这些变异等位基因以及我们先前报道的有关VKORC1 * 2,CYP2C9 * 2和CYP2C9 * 3多态性的数据,对于VKORC1 * 3,VKORC1 * 4和CYP4F2都没有显着关联(1347 C> T )。总之,在心肌梗死患者中,VKORC1 * 3,VKORC1 * 4和CYP4F2(1347 C> T)多态性对华法林剂量需求的个体贡献可忽略不计。我们的结果表明,与对VKORC1 * 3,VKORC1 * 4和CYP4F2(1347 C> T)多态性进行测试相比,对VKORC1 * 2,CYP2C9 * 2和CYP2C9 * 3进行药理学检测对华法令剂量的要求更为有用。

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