Noncanonical Effects of Oral Thrombin and Factor Xa Inhibitors in Platelet Activation and Arterial Thrombosis.
Animals
Blood Coagulation
/ drug effects
Dabigatran
/ therapeutic use
Factor Xa Inhibitors
/ therapeutic use
Humans
Platelet Activation
/ drug effects
Pyrazoles
/ therapeutic use
Pyridines
/ therapeutic use
Pyridones
/ therapeutic use
Rivaroxaban
/ therapeutic use
Thiazoles
/ therapeutic use
Thrombosis
/ blood
Journal
Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
pubmed:
18
9
2020
medline:
9
10
2021
entrez:
17
9
2020
Statut:
ppublish
Résumé
Nonvitamin K oral anticoagulants (NOACs) or direct oral anticoagulants comprise inhibitors of factor Xa (rivaroxaban, apixaban, edoxaban) or factor IIa (dabigatran). Both classes efficiently interfere with the final or penultimate step of the coagulation cascade and showed superior net clinical benefit compared with vitamin K antagonists for prevention of thromboembolic events in patients with AF and for prevention and therapy of deep vein thrombosis and pulmonary embolism. None the less, accumulating data suggested, that there may be differences regarding the frequency of atherothrombotic cardiovascular events between NOACs. Thus, the optimal individualized NOAC for each patient remains a matter of debate. Against this background, some basic and translational analyses emphasized NOAC effects that impact on platelet activity and arterial thrombus formation beyond inhibition of plasmatic coagulation. In this review, we will provide an overview of the available clinical and translational evidence for so-called noncanonical NOAC effects on platelet activation and arterial thrombosis.
Identifiants
pubmed: 32942315
doi: 10.1055/s-0040-1716750
doi:
Substances chimiques
Factor Xa Inhibitors
0
Pyrazoles
0
Pyridines
0
Pyridones
0
Thiazoles
0
apixaban
3Z9Y7UWC1J
Rivaroxaban
9NDF7JZ4M3
Dabigatran
I0VM4M70GC
edoxaban
NDU3J18APO
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
122-130Subventions
Organisme : 18-2019
ID : Forschungskommission of the Medical Faculty of the Heinrich Heine University
Organisme : 2019-29
ID : Forschungskommission of the Medical Faculty of the Heinrich Heine University
Organisme : 2018-32
ID : Forschungskommission of the Medical Faculty of the Heinrich Heine University
Organisme : PO 2247/2-1
ID : German Research Foundation
Organisme : SFB1116
ID : German Research Foundation
Organisme : PE2704/2-1
ID : German Research Foundation
Organisme : F/04/19
ID : Deutsche Herzstiftung
Informations de copyright
Thieme. All rights reserved.
Déclaration de conflit d'intérêts
None declared.