Abstract

Warfarin is the most widely prescribed anticoagulant in the world. Patients who need more than 15 mg per day should be considered warfarin-resistant. Nearly 30 genes have been reported in association with warfarin pharmacogenetics but genetic polymorphisms in the genes encoding CYP2C9 and VKORC1 have been shown to act as the most important determinants of drug dosage requirements. The major enzyme responsible for the metabolism of S-warfarin, the more potent of warfarin’s two stereoisomers, is CYP2C9. Warfarin inhibits vitamin K epoxide reductase (VKOR). A 30-year-old woman was referred to our clinic for pulmonary embolism. She was treated with low molecular weight heparin. The warfarin dose was titrated up to 15 mg daily but after one week, the INR (international normalized ratio) was still subtherapeutic level at 1.8. In this paper, we discuss underlying genetic polymorphisms about warfarin resistance.

Details

Title
Warfarin Resistance: A Case Report
Author
Gönlügür, Uğur  VIAFID ORCID Logo  ; Gönlügür, Tanseli  VIAFID ORCID Logo  ; Öztürk Özdemir  VIAFID ORCID Logo  ; Sılan, Fatma  VIAFID ORCID Logo 
Pages
61-63
Section
Case Report
Publication year
2019
Publication date
Mar 2019
Publisher
Galenos Publishing House
ISSN
21495807
e-ISSN
21496048
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2369503061
Copyright
© 2019. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.