Pharmacogenetics of warfarin dosing in patients of African and European ancestry

被引:28
作者
Shendre, Aditi [1 ]
Dillon, Chrisly [2 ]
Limdi, Nita A. [2 ]
机构
[1] Indiana Univ Purdue Univ, Richard M Fairbanks Sch Publ Hlth, Dept Epidemiol, Indianapolis, IN 46202 USA
[2] Univ Alabama Birmingham, Dept Neurol, Sch Med, UAB Stn, Birmingham, AL 35294 USA
关键词
pharmacogenetic dosing algorithms; race; warfarin; REDUCTASE COMPLEX SUBUNIT-1; DOSE REQUIREMENTS; CYP2C9; GENOTYPE; ANTICOAGULATION CONTROL; AMERICAN INDIVIDUALS; GENETIC-VARIANTS; RANDOMIZED-TRIAL; CLINICAL FACTORS; VKORC1; ALLELES; PILOT TRIAL;
D O I
10.2217/pgs-2018-0146
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the introduction of direct acting oral anticoagulants, warfarin remains the most commonly prescribed oral anticoagulant. However, warfarin therapy is plagued by the large inter- and intrapatient variability. The variability in dosing fueled research to identify clinical and genetic predictors and develop more accurate dosing algorithms. Observational studies have demonstrated the significant impact of single nucleotide polymorphisms in CYP2C9 and VKORC1 on warfarin dose in patients of European ancestry and African-Americans. This evidence supported the design and conduct of clinical trials to assess whether genotype-guided dosing results in improved anticoagulation control and outcomes. The trial results have shown discordance by race, with pharmacogenetic algorithms improving dose and anticoagulation control among European ancestry patients compared with African-American patients. Herein, we review the evidence from observational and interventional studies, highlight the need for inclusion of minority race groups and propose the need to develop race specific dosing algorithms.
引用
收藏
页码:1357 / 1371
页数:15
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