Effect of CYP2C9 *11/*11 genotype on initial and long-term warfarin dose requirement and therapeutic response

Pharmacogenomics. 2020 Dec;21(18):1271-1277. doi: 10.2217/pgs-2020-0125. Epub 2020 Dec 2.

Abstract

The warfarin dose requirement and therapeutic response of a 42-year-old African-American male with genotype CYP2C9 *11/*11, VKORC1 -1639GG and CYP4F2 433Val/Val anticoagulated for ischemic stroke is described herein. Warfarin was dosed according to the institution's personalized medicine program recommendations of a 10 mg mini-load dose, followed by dose decreases to 4-6 mg/day through discharge. Stable international normalized ratio was achieved after eight doses, with good overall long-term maintenance of therapeutic international normalized ratio over several years with warfarin doses of 3.1-4.3 mg/day. This case report sheds further light on the clinical impact of CYP2C9 *11/*11 on warfarin dose requirements, short- and long-term treatment response and practical considerations for warfarin management in suspected carriers of rare variant CYP2C9 alleles.

Keywords: CYP2C9*11; anticoagulation; pharmacogenetics; stroke; warfarin.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Ambulatory Care
  • Anticoagulants / administration & dosage*
  • Anticoagulants / therapeutic use*
  • Cytochrome P-450 CYP2C9 / genetics*
  • Gene Frequency
  • Genotype
  • Humans
  • Hypertension / complications
  • Hypertension / drug therapy
  • International Normalized Ratio
  • Ischemic Stroke / drug therapy*
  • Male
  • Precision Medicine
  • Warfarin / administration & dosage*
  • Warfarin / therapeutic use*

Substances

  • Anticoagulants
  • Warfarin
  • CYP2C9 protein, human
  • Cytochrome P-450 CYP2C9