[Study of variability in response to aspirin and clopidogrel: clinical and/or biological resistance?]

M-M Samama1, I Elalamy

  • 1Service d'hématologie biologique, Hôtel-Dieu, 75004 Paris, France. mmsamama@aol.com

Insights

Millions in France use aspirin and clopidogrel for secondary prevention of thrombotic events. Researchers suggest using "variable platelet response" instead of "resistance" for clarity and potential prognostic insights.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Medicine

Background:

  • Aspirin and clopidogrel are widely used long-term antiplatelet therapies in France.
  • These drugs are crucial for secondary prevention following arterial thrombotic events like myocardial infarction and stroke.
  • The concept of 'resistance' to these drugs is often ambiguously defined and applied.

Purpose of the Study:

  • To address the confusion surrounding the term 'resistance' in antiplatelet therapy.
  • To advocate for the adoption of 'variable platelet response' as a more accurate and accepted term.
  • To explore the clinical relevance of differentiating between true resistance and variable response.

Main Methods:

  • Review of existing biological and clinical literature on antiplatelet drug response.
  • Discussion of various platelet function tests used to assess treatment impact.
  • Consideration of ongoing large-scale prospective studies.

Main Results:

  • True pharmacological resistance to aspirin and clopidogrel is considered rare.
  • A variable platelet response is a more common phenomenon observed in patients.
  • Distinguishing between resistance and variable response may have significant prognostic implications.

Conclusions:

  • The term 'variable platelet response' is preferred over 'resistance' for better clarity and acceptance among specialists.
  • Platelet function tests are valuable tools for evaluating the biological effects of antiplatelet treatments.
  • Further research and results from ongoing studies are necessary to establish clinical guidelines for optimal antiplatelet therapy based on response variability.

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