Генотип СС гена vKORC1 ассоциируется с активацией каскада коагуляции и снижением фибринолитической активности у пациентов с фибрилляцией предсердий

This article is related to investigation of the associations between VKORC1 C1173T gene polymorphism and haemostatic indicators in patients with permanent atrial fibrillation. There were studied 182 patients with coronary heart disease and permanent atrial fibrillation; mean age was 64±9.8 years. The study showed that in patients with permanent atrial fibrillation the presence of VKORC1 CC genotype was accompanied by an increase of thrombin-activatable fibrinolysis inhibitor of more than 205% and also soluble fibrin monomer complexes of more than 10 mg%.