The effect of CYP2C9*2, CYP2C9*3, and VKORC1-1639 G>A polymorphism in patients under warfarin therapy in city of Kermanshah
Autor: | Ali Fattahi, Mona Sadeghalvad, Reza Khodarahmi, Fathemeh Norooznezhad, Azadeh Mahnam, Zohreh Hosseinkhani, Mohammad Fazilati, Kamran Mansouri |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Vitamin K1 epoxide reductase Population Gastroenterology 03 medical and health sciences 0302 clinical medicine Pharmacy and materia medica Internal medicine Genotype medicine General Pharmacology Toxicology and Pharmaceutics Allele International normalized ratio Polymorphism education Genotyping CYP2C9 Cytochrome P-450 CYP2C9 education.field_of_study biology Warfarin CYP2C9*3 RS1-441 030104 developmental biology 030220 oncology & carcinogenesis biology.protein Original Article cytochrome p-450 cyp2c9 international normalized ratio polymorphism vitamin k1 epoxide reductase warfarin VKORC1 medicine.drug |
Zdroj: | Research in Pharmaceutical Sciences, Vol 13, Iss 4, Pp 377-384 (2018) Research in Pharmaceutical Sciences |
ISSN: | 1735-9414 1735-5362 |
Popis: | Polymorphism in the genes encoding CYP2C9 enzyme and VKORC1 reductase significantly influence warfarin dose requirement since patients with CYP2C9*2, CYP2C9*3 and VKORC1 mutant alleles require lower warfarin maintenance doses. Studies have reported the ethnic variations in the frequency of these genes within the various populations in Iran and other parts of the world. However, no such study has been done yet on Kurdish population in Kermanshah. From Kurdish population of Kermanshah province in Iran, a total of 110 patients who had heart surgery and taking warfarin, were genotyped for polymorphisms of VKORC1-1639 G>A, CYP2C9*2, and CYP2C9*3. Polymorphism genotyping was performed by sequencing as well as polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) using restriction enzymes of MspI, AVAII and KpnI, respectively. The frequencies of VKORC1-1639 GG, GA, and AA genotypes were 42%, 36%, and 22%, respectively and for CYP2C9 1*/1*, 1*/2*, 2*/2*, 1*/3*, 3*/3*, 2*/3* were 71%, 17%, 5.4%, 1.8%, 4.5%, and 0%, respectively. The frequency of VKORC1-1639A allele was 42.3% and the frequencies of CYP2C9*2 and *3 alleles were 14% and 5.4%, respectively. It was indicated that low warfarin dose requirements are strongly associated with the presence of CYP2C9 and VKORC1-1639 variant alleles. Our results confirmed the supply to understand the distribution of genomic biomarkers related to the drugs metabolism for future planning health programs. |
Databáze: | OpenAIRE |
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