Eurasian Journal of Emergency Medicine

Warfarin resistance: A case report. [JAEM]
JAEM. 2019; 18(1): 61-63

Warfarin resistance: A case report.

Uğur Gönlügür1, Tanseli Gönlügür2, Ozturk Ozdemir3, Fatma Silan3
1Department Of Chest Diseases, Canakkale Onsekiz Mart University, Canakkale, Turkey
2Department Of Chest Diseases, Canakkale City Hospital, Canakkale, Turkey
3Department Of Medical Genetics, Canakkale Onsekiz Mart University, Canakkale, Turkey

Warfarin is the most widely used 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 major determinants of drug dosage requirements. The main enzyme responsible for the metabolism of S-warfarin, the more potent of warfarin’s two stereoisomers, is CYP2C9. Vitamin K [ep]oxide reductase (VKOR) is the enzyme that warfarin inhibits. 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.

Keywords: Warfarin, Vitamin K Epoxide Reductases, VKORC1, anticoagulants


Uğur Gönlügür, Tanseli Gönlügür, Ozturk Ozdemir, Fatma Silan. Warfarin resistance: A case report.. JAEM. 2019; 18(1): 61-63

Corresponding Author: Uğur Gönlügür, Türkiye


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