Genotype-guided coumarin dosing: Where are we now and where do we need to go next?

Publication date

2015-04-01

Authors

Baranova, Ekaterina V.ISNI 0000000493301194
Verhoef, TalithaISNI 0000000394802807
Asselbergs, Folkert W.
De Boer, AnthoniusISNI 0000000389596105
Maitland - van der Zee, Anke-HilseISNI 0000000376188831

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Advisors

Supervisors

Document Type

Book review
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taverne

Abstract

Introduction: A large proportion of the coumarin dose variability is explained by environmental factors and by common genetic variants in the VKORC1 and CYP2C9 genes. Genotype-guided coumarin dosing has been proposed for a more accurate prediction of the coumarin dose in order to reduce the incidence of coumarin-related complications.Areas covered: This review discusses the current state of coumarin pharmacogenetics, the evidence from recent randomized controlled trials and economic evaluations regarding the possible clinical implementation of genotype-guided coumarin dosing.Expert opinion: When the VKORC1 and CYP2C9 genotypes are available before the start of coumarin therapy in individuals of European ancestry, a genetic-guided algorithm should be used for dose determination. Ethnicity-specific pharmacogenetic algorithms should be tested in other populations. At this moment the evidence is not sufficient to support genotyping before coumarin therapy initiation. Based on results from recent randomized controlled trials, a clinical dosing algorithm could be considered in the initial phase of coumarin treatment. Current economic studies indicate that genotype-guided dosing could be cost-effective, but the clinical implementation of genetic-guided coumarin therapy will depend on the cost of pharmacogenetic tests and the availability of novel oral anticoagulants.

Keywords

Coumarins, CYP2C9, Dose, Genetic-guided, Pharmacogenetics, Polymorphism, VKORC1, Warfarin, NCT00964353, acenocoumarol, amiodarone, coumarin derivative, cytochrome P450 2C9, dabigatran, phenprocoumon, vitamin K epoxide reductase, warfarin, algorithm, cost effectiveness analysis, genetic association, genetic variability, genotype, human, meta analysis (topic), multicenter study (topic), pharmacogenomics, prediction, randomized controlled trial (topic), review, single nucleotide polymorphism, Taverne

Citation

Baranova, E V, Verhoef, T I, Asselbergs, F W, De Boer, A & Maitland-Van Der Zee, A-H 2015, 'Genotype-guided coumarin dosing: Where are we now and where do we need to go next?', Expert Opinion on Drug Metabolism and Toxicology, vol. 11, no. 4, pp. 509-522. https://doi.org/10.1517/17425255.2015.1004053