P2Y12 receptor inhibitors: an evolution in drug design to prevent arterial thrombosis

Danny Kupka1,2, Dirk Sibbing1,2

  • 1a Department of Cardiology , LMU München , Munich , Germany.

Abstract

Insights

Dual antiplatelet therapy (DAPT) with P2Y12 inhibitors prevents arterial thrombosis in acute coronary syndromes (ACS). Current drugs balance bleeding risk and efficacy, guiding future individualized treatment strategies.

Area of Science:

  • Cardiology
  • Pharmacology
  • Thrombosis

Background:

  • P2Y12 inhibitors are essential for dual antiplatelet therapy (DAPT) in acute coronary syndromes (ACS) and after stent implantation.
  • This review covers P2Y12 receptor biology and current inhibitors, including clopidogrel, prasugrel, ticagrelor, and cangrelor.
  • The challenge lies in balancing arterial thrombosis prevention with bleeding events.

Purpose of the Study:

  • To review current knowledge on P2Y12 receptor inhibitors.
  • To summarize data from preclinical and clinical trials of approved P2Y12 inhibitors.
  • To provide strategies for drug switching and bleeding event management.

Main Methods:

  • Literature search of basic science articles, clinical studies, and reviews (1992-2017) using PubMed.
  • Analysis of data from preclinical and clinical trials of clopidogrel, prasugrel, ticagrelor, and cangrelor.
  • Synthesis of information on purinergic receptor biology and P2Y12 inhibitor applications.

Main Results:

  • P2Y12 inhibitors are crucial for DAPT in ACS patients undergoing stenting.
  • Approved P2Y12 inhibitors (clopidogrel, prasugrel, ticagrelor, cangrelor) are standard care but associated with bleeding.
  • Data supports strategies for drug switching and managing bleeding events.

Conclusions:

  • Extensive data exists for P2Y12 inhibitor use in DAPT for ACS.
  • Prasugrel, ticagrelor, and clopidogrel are current standards but carry bleeding risks.
  • Future trials will inform individualized P2Y12 inhibitor therapy, optimizing escalation and de-escalation strategies.

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