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VKORC1和CYP2C9基因多态性与接受心脏瓣膜置换手术的伊朗代表性人群华法林剂量需求的关联

Association of VKORC1 and CYP2C9 gene polymorphisms with warfarin dose requirements in a representative Iranian population with cardiac valve replacement surgery.

作者信息

Maleki Omid, Gharechahi Javad

机构信息

Student Research Committee.

Human Genetics Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Pharmacogenet Genomics. 2025 Sep 1;35(7):214-220. doi: 10.1097/FPC.0000000000000571. Epub 2025 Jun 13.

DOI:10.1097/FPC.0000000000000571
PMID:40511772
Abstract

BACKGROUND

Warfarin is a commonly used oral anticoagulant for managing thromboembolic events after cardiac valve surgery. However, its optimal dose varies between individuals, often requiring trial and error to determine. This study aimed to investigate the association of polymorphisms in the CYP2C9 and VKORC1 genes with warfarin dose requirements in an Iranian population undergoing cardiac valve replacement.

MATERIALS AND METHODS

A total of 140 patients recieving warfarin after cardiac valve replacement surgery were enrolled. Patients were monitored for their daily warfarin dose and international normalized ratio for at least 3 months post-surgery. Genotyping of CYP2C9 rs1057910 and VKORC1 rs2884737 was conducted using the tetra-primer amplification refractory mutation system -PCR method. Associations between genotypes and warfarin dose were analyzed using linear regression. A P value < 0.05 was considered statistically significant.

RESULTS

Patients with the heterozygous AC genotype of CYP2C9 rs1057910 required a significantly lower warfarin dose than those with the wild-type genotype ( P < 0.05). Although variation in warfarin dose was observed among patients with different VKORC1 rs2884737 genotypes, the association was not statistically significant. Including patients' demographic covariates in the regression model did not alter the observed genotype-dose associations.

CONCLUSION

The CYP2C9 rs1057910 variant was significantly associated with daily warfarin dose requirements, suggesting its potential role in guiding idividualized dosing. In contrast, VKORC1 rs2884737 showed no significant association in this population, despite previous findings in other ethnic groups.

摘要

背景

华法林是心脏瓣膜置换术后用于预防血栓栓塞事件的常用口服抗凝剂。然而,其最佳剂量因人而异,通常需要反复试验来确定。本研究旨在调查伊朗接受心脏瓣膜置换术人群中CYP2C9和VKORC1基因多态性与华法林剂量需求之间的关联。

材料与方法

共纳入140例心脏瓣膜置换术后接受华法林治疗的患者。术后至少3个月监测患者每日华法林剂量及国际标准化比值。采用四引物扩增阻滞突变系统-PCR方法对CYP2C9 rs1057910和VKORC1 rs2884737进行基因分型。采用线性回归分析基因型与华法林剂量之间的关联。P值<0.05被认为具有统计学意义。

结果

CYP2C9 rs1057910杂合子AC基因型患者所需华法林剂量显著低于野生型基因型患者(P<0.05)。虽然不同VKORC1 rs2884737基因型患者的华法林剂量存在差异,但该关联无统计学意义。在回归模型中纳入患者的人口统计学协变量并未改变观察到的基因型-剂量关联。

结论

CYP2C9 rs1057910变异与每日华法林剂量需求显著相关,表明其在指导个体化给药方面的潜在作用。相比之下,尽管在其他种族群体中有先前的研究结果,但VKORC1 rs2884737在该人群中未显示出显著关联。

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