نتایج جستجو برای: vkorc1

تعداد نتایج: 527  

2010
Zoraida Verde Jonatan R. Ruiz Catalina Santiago Beatriz Valle Fernando Bandrés Elpidio Calvo Alejandro Lucía Félix Gómez Gallego

The identification of CYP2C9 and VKORC1 genes has strongly stimulated the research on pharmacogenetics of coumarins in the last decade. We assessed the combined influence of CYP2C9 *2 and *3, and VKORC1 c.-1639G>A, 497C>G, and 1173C>T variants, on acenocoumarol dosage using a novel algorithm approach, in 193 outpatients who had achieved stable anticoagulation. We constructed an "acenocoumarol-d...

Journal: :Clinical chemistry 2009
Tohru Aomori Koujirou Yamamoto Atsuko Oguchi-Katayama Yuki Kawai Takefumi Ishidao Yasumasa Mitani Yasushi Kogo Alexander Lezhava Yukiyoshi Fujita Kyoko Obayashi Katsunori Nakamura Hugo Kohnke Mia Wadelius Lena Ekström Cristine Skogastierna Anders Rane Masahiko Kurabayashi Masami Murakami Paul E Cizdziel Yoshihide Hayashizaki Ryuya Horiuchi

BACKGROUND Polymorphisms of the CYP2C9 (cytochrome P450, family 2, subfamily C, polypeptide 9) gene (CYP2C9*2, CYP2C9*3) and the VKORC1 (vitamin K epoxide reductase complex, subunit 1) gene (-1639G>A) greatly impact the maintenance dose for the drug warfarin. Prescreening patients for their genotypes before prescribing the drug facilitates a faster individualized determination of the proper mai...

Journal: :Hematology. American Society of Hematology. Education Program 2006
Brian F Gage

To reduce the risk of hemorrhage, experts advocate prescribing the anticipated therapeutic dose to patients who are beginning coumarin therapy, but until now there was no accurate way to estimate that dose. Using pharmacogenetics-based coumarin therapy, clinicians can now estimate the therapeutic dose by genotyping their patients for single nucleotide polymorphisms (SNPs) that affect coumarin m...

Journal: :Clinical pharmacology and therapeutics 2010
P Lenzini M Wadelius S Kimmel J L Anderson A L Jorgensen M Pirmohamed M D Caldwell N Limdi J K Burmester M B Dowd P Angchaisuksiri A R Bass J Chen N Eriksson A Rane J D Lindh J F Carlquist B D Horne G Grice P E Milligan C Eby J Shin H Kim D Kurnik C M Stein G McMillin R C Pendleton R L Berg P Deloukas B F Gage

Well-characterized genes that affect warfarin metabolism (cytochrome P450 (CYP) 2C9) and sensitivity (vitamin K epoxide reductase complex 1 (VKORC1)) explain one-third of the variability in therapeutic dose before the international normalized ratio (INR) is measured. To determine genotypic relevance after INR becomes available, we derived clinical and pharmacogenetic refinement algorithms on th...

2012
Yumiko Akamine Tsukasa Uno

Warfarin, a coumarin vitamin K antagonist, is the most widely prescribed anticoagulant agent for the control and prevention of atrial fibrillation-related thrombus formation, stroke, and arterial and venous thrombembolism (Hirsh J et al., 1998). The recommend warfarin therapy consists of the lowest dose required to maintain the target international normalized ratio (INR) because of the drug’s n...

A high prevalence of genetic polymorphisms increases sensitivity to warfarin therapy. In this study, we investigated 47 patients with effective long-term therapy by warfarin well-controlled by monitoring of International Normalised Ratio (INR). All patients were tested for gene polymorphisms VKORC1, CYP2C9*C2, and CYP2C9*C3, which were used for a dose calculation employing a program www.Warfari...

Background and Aims: Warfarin is an anticoagulant agent used for many years in treating various clinical conditions such as thromboembolisms in cardiovascular disease. Some patients require different doses of warfarin to reach the therapeutic international normalized ratio ratio. These patients have specific demographic characteristics. Genetic polymorphisms in specific genes have been reported...

Journal: :Human molecular genetics 2006
Sharon Marsh Howard L McLeod

The field of pharmacogenomics has seen some exciting advances in the recent past. The Human Genome Project and International HapMap projects have uncovered a wealth of information for researchers. The discovery of clinically predictive genotypes (e.g. UGT1A1*28, TYMS TSER), haplotypes (e.g. VKORC1 Haplotype A) and somatic mutations (e.g. epidermal growth factor receptor), along with the introdu...

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