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The role of the polymorphism of CYP2C9 in Warfarin anticoagulation therapy for patients with atrial fibrillation |
LYU You YANG Jiefu |
Department of Caidiology, Beijing Hospital, Beijing 100730, China |
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Abstract Objective To investigate the significance of CYP2C9 gene polymorphism in Warfarin anticoagulation therapy for patients with atrial fibrillation, in order to explore the causes of Warfarin individual difference. Methods The 3rd and 7th exon of CYP2C9 in 100 patients with atrial fibrillation given Warfarin anticoagulation therapy in Beijing Hospital were detected by PCR and restriction enzyme digestion. The genotype and allelic frequencies were calculated and patients information, coagulation function and the individual Warfarin dosage requirements were recorded. Results In this group of patients with atrial fibrillation given Warfarin anticoagulation therapy, two kinds of allele were detected: CYP2C9*1 and CYP2C9*3, the frequency of *1 allele and *3 allele was 96% and 4% respectively. CYP2C9*1/*1 was the most common genotype, with the frequency of 92%. The frequency of CYP2C9*1/*3 was 8% in these 100 patients. After similar target INR range (2.0-3.0) achieved, variant CYP2C9*1/*3 homozygotes or heterozygotes required lower daily mean maintain doses [(2.14±0.55) mg] than wild-type CYP2C9*1/*1 patients did [(3.17±0.74) mg], with statistically significant difference (P < 0.05). Conclusion Polymorphism of CYP2C9 is associated with Warfarin dose requirements in patients with atrial fibrillation, which is partly the factor causing Warfarin individual difference .
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