4.2 Article

Case report: dose adjustment of warfarin using genetic information and plasma concentration monitoring

Journal

JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
Volume 39, Issue 3, Pages 319-321

Publisher

WILEY
DOI: 10.1111/jcpt.12135

Keywords

pharmacy practice; Japanese patient; vitamin K epoxide reductase complex, subunit 1; warfarin; cytochrome P450 2C9; therapeutic drug monitoring; pharmacogenetics; carbamazepine

Funding

  1. Grants-in-Aid for Scientific Research [25670049] Funding Source: KAKEN

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What is known and objective Carbamazepine is known to interact with warfarin. We report on a case of this interaction and on its management using the patient's genetic information. Case summary The case concerns a 74-year-old Japanese woman with a mood disorder and a central retinal vein occlusion. She was on therapy that included carbamazepine and had started to take warfarin. However, the patient's prothrombin time expressed as the international normalized ratio (PT-INR) was 1 center dot 40 despite taking a dose three times higher than the average. The patient's S-warfarin concentration was 0 center dot 15 mu g/mL and R-warfarin was 0 center dot 52 mu g/mL. Her cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase complex, subunit 1 (VKORC1), genotypes were *1/*1 and -1639GA, respectively. The VKORC1 genotype indicated that she would require an even higher dose. We proposed a further increase in dose and the patient's PT-INR rose to 1 center dot 99. What is new and conclusion The patient required a high warfarin dose because of the VKORC1 genotype, and induction of CYP2C9 by carbamazepine. We improved the patient's pharmacotherapy based on her genetic information.

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