Author/Authors :
Khosropanah, Shahdah School of Medicine - Shiraz University of medical science, Shiraz, Iran , Faraji, Nooreddin School of Advanced Medical Sciences and Technologies - Shiraz University of Medical Sciences, Shiraz, Iran , Habibi, Hamzeh School of Medicine - Shiraz University of medical science, Shiraz, Iran , Yavarian, Majid School of Medicine - Shiraz University of medical science, Shiraz, Iran , Mansoori, Roohollah School of Medicine - Shiraz University of medical science, Shiraz, Iran , Haghpanah, Sezaneh Namazi hospital - Shiraz University of Medical Sciences, Shiraz, Iran
Abstract :
Many cardiovascular diseases may require lifelong anticoagulation therapy. Warfarin is the
most prescribed medication in this regard with serious side effects in some patients. Several
single nucleotide polymorphisms (SNPs) affecting cytochrome P450 system can impact on
warfarin metabolism and dosing. 230 cardiovascular patients have participated in the study.
The INR levels were 1.5 to 3.5 with a mean range of 2.8. The subjects were divided into two
case and control groups. The rs2108622 SNP of the CYP4F2 gene and its effect on warfarin
dose requirements in these patients was evaluated.The results of our study showed a correlation
between age and warfarin dosage. The overall frequency of the CC and TT allele of rs2108622
was 53.1% and 18.6%. Daily average dose of warfarin in CC, CT and TT variants was 3.5 ±
1.6, 4.5 ± 2.1 and 5.3 ± 2.1 respectively. The daily warfarin dose in patients with CC allele was
significantly lower than that for CT or TT. The patients with TT allele required a 1.8 mg/day
higher dose of warfarin than that of CC.While there are many studies regarding relation of age
and warfarin dose, however, there are contradictory results about pharmacogentic status and
warfarin dose in different ethnics. Our study demonstrates that polymorphism in the CYP4F2
rs2108622 has a significant impact on the warfarin requirements in Iranian patients.
Keywords :
Cardiovascular disease , Warfarin , Polymorphism , CYP4F2 , rs2108622