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Prospective Study of Warfarin Dosage Requirements Based on Cyp2c9 and Vkorc1 Genotypes
Resource
CLINICAL PHARMACOLOGY & THERAPEUTICS v.84 n.1 pp.83-89
Journal
Clinical Pharmacology & Therapeutics
Pages
83-89
Date Issued
2008
Date
2008
Author(s)
WEN, MING-SHIEN
LEE, MING-TA MICHAEL
CHEN, JIN-JER
CHUANG, HUI-PING
LU, LIANG-SUEI
CHEN, CHIEN-HSIUN
LEE, TSONG-HAI
KUO, CHI-TAI
KUAN, PEI-LIANG
CHEN, YING-FU
WU, JER-YUARN
CHEN, YUAN-TSONG
Abstract
Polymorphisms in CYP 2C9 and VKOR C1 have been shown to be associated with warfarin dose requirements and could be used to predict warfarin dose . We conducted a prospective study in which warfarin dose was prescribed based on CYP 2C9 and VKOR C1 polymorphisms in 108 Han-Chinese patients without prior warfarin treatments. Using the genotype-based dosing, 83% of patients reached stable, therapeutic international normalized ratio (INR ) within 2 weeks of treatment initiation and none of the patients developed clinical bleeding or thromboembolic event. Ten percent (11) of patients with INR >4 and no clinical bleeding were detected during this study. At 12 weeks, 69% of the patients’maintenance doses matched the prediction. Dosing algorithms incorporating genetic factors, age, and body surface area were developed, which could explain up to 62% of the total variation (R2 of 0.62). This study demonstrated that pharmacogenetics- based dosing could improve time to stable, therapeutic INR , reduce adverse events, and achieve high sensitivity.
Type
journal article