Assessment, mechanisms, and clinical implication of variability in platelet response to aspirin and clopidogrel

Itsik Ben-Dor1, Neal S Kleiman, Eli Lev

  • 1Department of Cardiology, Rabin Medical Center and Tel Aviv University, Tel Aviv, Israel.

Insights

Low responsiveness to antiplatelet drugs like aspirin and clopidogrel can lead to adverse cardiac events. Optimizing treatment for patients with low drug response is crucial for cardiovascular disease management.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology
  • Clinical Laboratory Science

Background:

  • Antiplatelet therapy (aspirin and clopidogrel) is standard for cardiovascular disease (CVD).
  • Some patients have adverse cardiac events despite antiplatelet therapy, potentially due to low drug responsiveness.
  • Reported incidence of low responsiveness varies widely (1-45%) due to inconsistent testing methods.

Purpose of the Study:

  • To review laboratory testing of antiplatelet response to aspirin and clopidogrel.
  • To examine the prevalence, mechanisms, and clinical significance of low antiplatelet response.
  • To explore alternative strategies for optimizing antiplatelet therapy in non-responsive patients.

Main Methods:

  • Review of literature on antiplatelet drug response testing.
  • Analysis of studies investigating the link between low responsiveness and cardiovascular events.
  • Discussion of diagnostic challenges and therapeutic implications.

Main Results:

  • Low responsiveness to aspirin or clopidogrel is linked to increased cardiovascular events.
  • Evidence for this association is stronger for clopidogrel than aspirin.
  • No established therapeutic approach currently exists for managing low antiplatelet response.

Conclusions:

  • Low responsiveness to antiplatelet agents is a significant clinical concern in CVD.
  • Standardized testing and validated therapeutic strategies are needed.
  • Further research is required to optimize treatment for patients with suboptimal antiplatelet response.

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