Targeting factor Xa and thrombin: impact on coagulation and beyond

CT Esmon - Thrombosis and haemostasis, 2014 - thieme-connect.com
CT Esmon
Thrombosis and haemostasis, 2014thieme-connect.com
Great advances have been made in recent years in understanding the haemostatic system
and the molecular and cellular basis of thrombus formation. Although directly targeting factor
Xa or thrombin (factor IIa) for effective anticoagulation is now well established, evidence has
emerged suggesting that factor Xa and thrombin are involved in other physiological and
pathophysiological cellular processes, including inflammation. These non-haemostatic
activities of factor Xa and thrombin are predominantly mediated via the activation of …
Great advances have been made in recent years in understanding the haemostatic system and the molecular and cellular basis of thrombus formation. Although directly targeting factor Xa or thrombin (factor IIa) for effective anticoagulation is now well established, evidence has emerged suggesting that factor Xa and thrombin are involved in other physiological and pathophysiological cellular processes, including inflammation. These non-haemostatic activities of factor Xa and thrombin are predominantly mediated via the activation of proteinaseactivated receptors. Studies have indicated a potential role of coagulation proteins (including factor Xa and thrombin) in the progression of disease conditions such as atherothrombosis. Preclinical studies have provided evidence for the effects of direct factor Xa or direct thrombin inhibition beyond anticoagulation, including anti-inflammatory activities and atherosclerotic plaque stabilisation. In this article, the non-haemostatic activities of factor Xa and thrombin and the effects of direct inhibition of these coagulation factors on these activities are summarised. In addition, the potential roles of factor Xa and thrombin in atherosclerosis and atherothrombosis are explored and the cardiovascular profiles of rivaroxaban, apixaban and dabigatran etexilate observed in phase III clinical studies are discussed.
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