Pharmacogenetic relevance of CYP4F2 V433M polymorphism on acenocoumarol therapy

• Published in: Blood Vol. 113; no. 20; pp. 4977 - 4979
• Main Authors: Pérez-Andreu, Virginia, Roldán, Vanessa, Antón, Ana Isabel, García-Barberá, Nuria, Corral, Javier, Vicente, Vicente, González-Conejero, Rocio
• Format: Journal Article
• Language: English
• Published: Washington, DC Elsevier Inc 14.05.2009; Americain Society of Hematology
• Subjects: Acenocoumarol - administration & dosage; Acenocoumarol - therapeutic use; Aged; Anticoagulants - administration & dosage; Anticoagulants - therapeutic use; Biological and medical sciences; Blood Coagulation Tests; Cytochrome P-450 Enzyme System - genetics; Cytochrome P450 Family 4; Drug Dosage Calculations; Drug Resistance - genetics; Genotype; Hematologic and hematopoietic diseases; Humans; Male; Medical sciences; Methionine - genetics; Middle Aged; Mixed Function Oxygenases - genetics; Pharmacogenetics; Polymorphism, Single Nucleotide - physiology; Time Factors; Valine - genetics; Vitamin K Epoxide Reductases; Antivitamin K; Pharmacogenetics; Treatment; Genetic variability; Hematology; Coumarine derivatives; Genetics; Genotype; Acenocoumarol; Polymorphism
• ISSN: 0006-4971; 1528-0020; 1528-0020
• DOI: 10.1182/blood-2008-09-176222

VKORC1 and CYP2C9 polymorphisms are used to predict the safe dose of oral anticoagulant therapy. A new variant of CYP4F2 (V433M) has recently been related to the required warfarin dose. We evaluated its influence in earliest response to acenocoumarol in 100 selected men who started anticoagulation (3 mg for 3 consecutive days). V433M genotype exerted a gene dosage-dependent effect on the decrease of factors II, VII, IX, and X in the earliest response to acenocoumarol, with homozygous 433V subjects being the most sensitive. Similarly, after the initiation of therapy, international normalized ratio also experienced a gene dosage-dependent effect (P = .015), and 433V subjects needed 4 mg/week less than 433M carriers to achieve a steady anticoagulation (P = .043). Multivariate linear regression analysis revealed a significant contribution of V433M polymorphism to variability of both early international normalized ratio value (R2 = 0.14) and dose requirements (R2 = 0.19). Our data underline the relevant role of CYP4F2 V433M polymorphism in the pharmacogenetics of coumarin anticoagulants.