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Clinical application of a new warfarin-dosing regimen based on the CYP2C9 and VKORC1 genotypes in atrial fibrillation patients

机译:基于CYP2C9和VKORC1基因型的华法林给药新方案在房颤患者中的临床应用

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摘要

The polymorphisms of cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase complex 1 (VKORC1) are important genetic factors for warfarin dose determinations. The present study aimed to investigate the contribution of the CYP2C9 and VKORC1 genotypes to warfarin dose requirement in atrial fibrillation (AF) patients, and to evaluate the clinical application of a warfarin-dosing algorithm. A total of 122 AF patients with a target international normalized ratio of 2.0 to 3.0 were included to determine the genotypes of CYP2C9 (rs1057910) and VKORC1 (rs9923231). A warfarin-dosing algorithm was developed based on age, height, and the CYP2C9 and VKORC1 genotypes of AF patients. The results indicated that the mean warfarin daily dose requirement was lower in the CYP2C9*1/*3 genotype compared with those in the homozygous wild-type CYP2C9*1/*1 patients (P<0.05), and was higher in patients with the VKORC1 AG and GG genotypes compared with those with the AA genotype (P<0.05). The multivariate regression model showed that age, height, and the CYP2C9 and VKORC1 genotypes were the best variables for estimating warfarin dose (R2=56.4%). A new warfarin-dosing algorithm was developed and its validity was confirmed in a second cohort of AF patients. During the 50-day follow-up, 63.3% (19/30) of control group patients and 86.7% (26/30) of patients in the experimental group acquired the warfarin maintenance dose. Among all the patients who acquired the warfarin maintenance dose, the mean time elapse from initiation until warfarin maintenance dose was significantly less in the experimental group (25.8±1.7 day) compared to the control group (33.1±1.9 day) (P<0.05). There was significant linear correlation between predicted warfarin maintenance dose and actual dose (r=0.822, P<0.01). In conclusion, a new warfarin-dosing algorithm was developed based on the CYP2C9 and VKORC1 genotypes, and it can shorten the time elapse from initiation until warfarin maintenance dose in AF patients with warfarin therapy.
机译:细胞色素P450 2C9(CYP2C9)和维生素K环氧还原酶复合物1(VKORC1)的多态性是确定华法林剂量的重要遗传因素。本研究旨在调查CYP2C9和VKORC1基因型对心房颤动(AF)患者华法林剂量需求的影响,并评估华法林给药算法的临床应用。纳入目标国际归一化比率为2.0:3.0的122位AF患者,以确定CYP2C9(rs1057910)和VKORC1(rs9923231)的基因型。根据年龄,身高以及房颤患者的CYP2C9和VKORC1基因型开发了一种华法林给药算法。结果表明,与纯合野生型CYP2C9 * 1 / * 1患者相比,CYP2C9 * 1 / * 3基因型的平均华法林日剂量需求量较低(P <0.05) VKORC1 AG和GG基因型与AA基因型相比(P <0.05)。多元回归模型显示年龄,身高,CYP2C9和VKORC1基因型是估计华法林剂量的最佳变量(R2 = 56.4%)。开发了一种新的华法林给药算法,并在第二批AF患者中证实了其有效性。在50天的随访期间,对照组的63.3%(19/30)和实验组的86.7%(26/30)的患者获得了华法林维持剂量。在获得华法林维持剂量的所有患者中,实验组(25.8±1.7天)从开始到华法林维持剂量的平均时间明显少于对照组(33.1±1.9天)(P <0.05) 。华法林维持剂量与实际剂量之间存在显着的线性相关性(r = 0.822,P <0.01)。总之,基于CYP2C9和VKORC1基因型,开发了一种新的华法林剂量算法,该算法可以缩短从开始使用华法林治疗的AF患者到华法林维持剂量的时间。

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