Pharmacogenetic-guided dosing of coumarin anticoagulants: algorithms for warfarin, acenocoumarol and phenprocoumon

被引:114
|
作者
Verhoef, Talitha I. [1 ]
Redekop, William K. [2 ]
Daly, Ann K. [3 ]
van Schie, Rianne M. F. [1 ]
de Boer, Anthonius [1 ]
Maitland-van der Zee, Anke-Hilse [1 ]
机构
[1] Univ Utrecht, Div Pharmacoepidemiol & Clin Pharmacol, Dept Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
[2] Erasmus Univ, Inst Med Technol Assessment, Rotterdam, Netherlands
[3] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
acenocoumarol; CYP2C9; pharmacogenetics; phenprocoumon; VKORC1; warfarin; EPOXIDE REDUCTASE COMPLEX; GENOME-WIDE ASSOCIATION; ORAL ANTICOAGULANTS; ATRIAL-FIBRILLATION; CYTOCHROME P4502C9; DOSE REQUIREMENTS; CYP2C9; GENOTYPE; COST-EFFECTIVENESS; VKORC1; GENOTYPES; BLEEDING RISK;
D O I
10.1111/bcp.12220
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Coumarin derivatives, such as warfarin, acenocoumarol and phenprocoumon are frequently prescribed oral anticoagulants to treat and prevent thromboembolism. Because there is a large inter-individual and intra-individual variability in dose-response and a small therapeutic window, treatment with coumarin derivatives is challenging. Certain polymorphisms in CYP2C9 and VKORC1 are associated with lower dose requirements and a higher risk of bleeding. In this review we describe the use of different coumarin derivatives, pharmacokinetic characteristics of these drugs and differences amongst the coumarins. We also describe the current clinical challenges and the role of pharmacogenetic factors. These genetic factors are used to develop dosing algorithms and can be used to predict the right coumarin dose. The effectiveness of this new dosing strategy is currently being investigated in clinical trials.
引用
收藏
页码:626 / 641
页数:16
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