Pharmacogenetic tests could be helpful in predicting of VKA maintenance dose in elderly patients at treatment initiation

• Published in: Journal of thrombosis and thrombolysis 2013, Vol.35 (1), p.90-94
• Main Authors: Kovac, Mirjana K., Rakicevic, Ljiljana B., Kusic-Tisma, Jelena S., Radojkovic, Dragica P.
• Format: Article
• Language: English
• Subjects: Age Factors; Aged; Aged, 80 and over; Alleles; Anticoagulants - administration & dosage; Anticoagulants - adverse effects; Aryl Hydrocarbon Hydroxylases - genetics; Aryl Hydrocarbon Hydroxylases - metabolism; Cardiology; Cytochrome P-450 CYP2C9; Female; Genotype; Hematology; Hemorrhage - chemically induced; Hemorrhage - genetics; Humans; International Normalized Ratio; Male; Medicine; Medicine & Public Health; Middle Aged; Mixed Function Oxygenases - genetics; Mixed Function Oxygenases - metabolism; Pharmacogenetics - methods; Vitamin K - antagonists & inhibitors; Vitamin K Epoxide Reductases
• ISSN: 0929-5305; 1573-742X
• DOI: 10.1007/s11239-012-0769-8

Several studies have linked mutations in the genes encoding cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase complex 1 (VKORC1) to a reduced VKA dose requirement and an increased risk of bleeding. Nevertheless, implementation of genotyping as a routine practice is still controversial. Our study was conducted in order to investigate the impact of genetic factors, presence of VKORC1-c.1639A, CYP2C*2 and CYP2C*3 among outpatients referred to Anticoagulation Service due to extremely unstable anticoagulant therapy. From 2008 to 2011, 68 patients, mean age 65.9, were included in the study. They were referred from primary care physicians due to inability to sustain the therapeutic range in the period of initiation of anticoagulant therapy. Genotyping results showed that 17 (25 %) of them were carriers of both CYP2C9 and VKORC1 variant alleles, 38 (55.9 %) were carriers of VKORC1 c.1639AA, 6 (8.8 %) were carriers of CYP2C9 variant alleles, while 7 (10.3 %) of them were carriers of wild type alleles. INR control upon admission showed that 34 (50 %) of them were over-anticoagulated, while 12 (17.6 %) of them had subsequent bleeding complications. Among over-anticoagulated patients, 32 were carriers of mutated alleles in both CYP2C9 and VKORC1 gene or VKORC1 alone, while 2 of patients carried wild type alleles. In addition to presence of CYP2C9 or VKORC 1 alleles, older age was an important factor related to a lower dose and risk for over-anticoagulation. Genotype (CYP2C9/VKORC1) and age are the most important factors that could predispose an extreme response and subsequent bleeding complications during the initiation of VKA.