Abstract | INTRODUCTION: METHODS AND RESULTS: Patients treated with dabigatran etexilate (n=22), rivaroxaban (n=24) or apixaban (n=22) were studied. Plasma was obtained before (trough) and 2h after drug intake (peak). Fibrinolytic resistance of clots exposed to exogenous tissue plasminogen activator was significantly lower in peak than in trough samples and correlated with drug concentration only in dabigatran group. Moreover, fibrinolytic resistance at peak was lower in dabigatran than in rivaroxaban and apixaban groups. This difference disappeared if the TAFI pathway was inhibited. Thrombin generation and TAFI activation were markedly lower in peak than in trough samples in all three groups. However, TAFIa levels in trough and peak samples were significantly lower in dabigatran group than in rivaroxaban and apixaban groups. Circulating levels of prothrombin fragment F1+2 (reflecting in vivo thrombin generation) and plasmin- antiplasmin complex (reflecting plasmin generation) were not or barely influenced by drug levels in all groups. CONCLUSIONS: Our data suggest that dabigatran, contrary to rivaroxaban and apixaban, reduces fibrinolytic resistance by virtue of its greater impact on TAFI activation. The profibrinolytic effect of dabigatran may play a role locally, at sites of fibrin formation, by making the nascent thrombus more susceptible to plasminogen-dependent degradation.
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Authors | Fabrizio Semeraro, Francesca Incampo, Concetta T Ammollo, Claudia Dellanoce, Oriana Paoletti, Sophie Testa, Mario Colucci |
Journal | Thrombosis research
(Thromb Res)
Vol. 138
Pg. 22-29
(Feb 2016)
ISSN: 1879-2472 [Electronic] United States |
PMID | 26826504
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Ltd. All rights reserved. |
Chemical References |
- Anticoagulants
- Antithrombins
- Factor Xa Inhibitors
- Pyrazoles
- Pyridones
- apixaban
- Rivaroxaban
- Carboxypeptidase B2
- Thrombin
- Dabigatran
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Topics |
- Aged
- Aged, 80 and over
- Anticoagulants
(therapeutic use)
- Antithrombins
(therapeutic use)
- Atrial Fibrillation
(blood, drug therapy, metabolism)
- Carboxypeptidase B2
(blood, metabolism)
- Dabigatran
(therapeutic use)
- Factor Xa Inhibitors
(therapeutic use)
- Female
- Fibrinolysis
(drug effects)
- Humans
- Male
- Pyrazoles
(therapeutic use)
- Pyridones
(therapeutic use)
- Rivaroxaban
(therapeutic use)
- Thrombin
(metabolism)
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