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Role for Thrombin Receptor Antagonism With Vorapaxar in Secondary Prevention of Atherothrombotic Events: From Bench to Bedside.

Abstract
In spite of treatment with the current standard of care antiplatelet regimens including dual antiplatelet therapy, recurrence rates of ischemic events remain elevated for high-risk patients with atherosclerotic disease. This may be in part attributed to the fact that other key platelet activation pathways remain uninhibited and can thus continue to trigger platelet activation and lead to thrombotic complications. Thrombin is a powerful inducer of platelet activation and mediates its effects directly on platelets through protease activator receptors (PARs), particularly the PAR-1 subtype, making PAR-1 inhibition an attractive approach for reducing atherothrombotic events. These observations have led to the development of several PAR-1 antagonists. Vorapaxar is a direct inhibitor of PAR-1 and the only agent of this class approved for the prevention of recurrent ischemic events in patients with prior myocardial infarction or peripheral artery disease. In the present manuscript, we present a review of the pathophysiologic role of thrombin on thrombotic complications, the impact of vorapaxar on outcomes, including the most recent updates deriving from clinical trials, as well as future perspectives in the field.
AuthorsJae Youn Moon, Francesco Franchi, Fabiana Rollini, Dominick J Angiolillo
JournalJournal of cardiovascular pharmacology and therapeutics (J Cardiovasc Pharmacol Ther) Vol. 23 Issue 1 Pg. 23-37 (Jan 2018) ISSN: 1940-4034 [Electronic] United States
PMID28565918 (Publication Type: Journal Article, Review)
Chemical References
  • Lactones
  • Platelet Aggregation Inhibitors
  • Pyridines
  • Receptor, PAR-1
  • Thrombin
  • vorapaxar
Topics
  • Atherosclerosis (drug therapy)
  • Humans
  • Lactones (pharmacology, therapeutic use)
  • Myocardial Infarction (drug therapy)
  • Myocardial Ischemia (prevention & control)
  • Peripheral Arterial Disease (drug therapy)
  • Platelet Aggregation Inhibitors (pharmacology, therapeutic use)
  • Pyridines (pharmacology, therapeutic use)
  • Receptor, PAR-1 (antagonists & inhibitors)
  • Secondary Prevention (methods)
  • Thrombin (metabolism)
  • Thrombosis (physiopathology, prevention & control)

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