Published in: First Personal Medical Congress
COI code: IPMCMED01_132
Paper Language: English
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Authors Polymorphism Detection of VKORC1 and CYP2C9 Genes in Iranian patients who are under warfarin therapyMasoumeh Dehghan Manshadi - National Institue of Genetic Engineering and Biotechnology
Omid Aryani - Iran University Medical Science Department of Neuroscience Tehran,Iran
Vadieh Ghodsinejad - National Institue of Genetic Engineering and Biotechnology
Arash Kadivari - National Institue of Genetic Engineering and Biotechnology
Abstract:Warfarin (Coumadin) is the most commonly used vitamin K antagonist. It has demonstrated effectiveness for the primary and secondary prevention of venous thromboembolism, for the prevention of systemic embolism in patients with prosthetic heart valves or atrial fibrillation, as an adjunct in the prophylaxis of systemic embolism after myocardial infarction, and for reducing the risk of recurrent myocardial infarction.Warfarin is metabolized primarily via oxidation in the liver by CYP2C9, and exerts its anticoagulant effect by inhibiting the protein vitamin K epoxide reductase complex, subunit 1 (VKORC1). Three single nucleotide polymorphisms (SNPs), two in the CYP2C9 gene and one in the VKORC1 gene, have been found to play key roles in determining the effect of warfarin therapy on coagulation.This study investigates the impact of these polymorphisms on 50 patients, referred to our Laboratory for determining the appropriate dose of warfarin. After DNA extraction of whole blood , PCR reverse dot blots technique was used to determine the polymorphism of CYP2C9 gene and VKORC1 gened in collected DNA samples. VKORC1 G/A was the most common genotype of VKORC1 allele among the study samples,with a rate of 56.2%. In CYP2C9 variant, 22% and 13.8% of subjects carried CYP2C9*1/*2 and CYP2C9*1/*3 genotyping, respectively.The results showed a significant relationship of the VCORC1 and CYP2C9 polymorphisms with warfarin sensitivity and severe side effects.
Keywords:CYP2C9 and VKORC1 polymorphisms, Polymerase Change Reaction, Warfarin dose requirements
COI code: IPMCMED01_132
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Dehghan Manshadi, Masoumeh; Omid Aryani; Vadieh Ghodsinejad & Arash Kadivari, 2016, Polymorphism Detection of VKORC1 and CYP2C9 Genes in Iranian patients who are under warfarin therapy, First Personal Medical Congress, تهران, دانشگاه علوم پزشكي ايران - پژوهشكده ملي مهندسي ژنتيك و زيست فناوري ايران، مركز همكاري هاي فناوري و نوآوري هاي رياست جمهوري, https://www.civilica.com/Paper-IPMCMED01-IPMCMED01_132.htmlInside the text, wherever referred to or an achievement of this article is mentioned, after mentioning the article, inside the parental, the following specifications are written.
First Time: (Dehghan Manshadi, Masoumeh; Omid Aryani; Vadieh Ghodsinejad & Arash Kadivari, 2016)
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