Monitoring aspirin and clopidogrel response: testing controversies and recommendations

Athanasios Karathanos1, Tobias Geisler

  • 1Department of Cardiology and Cardiovascular Medicine, University Hospital Tübingen, Ottfried-Müller-Straße 10, 72076, Tübingen, Germany.

Insights

Testing antiplatelet therapy effectiveness is crucial for coronary artery disease (CAD) patients. Assessing individual responses to clopidogrel and aspirin can help prevent adverse cardiac events and guide personalized treatment strategies.

Area of Science:

  • Cardiology
  • Pharmacogenomics

Background:

  • Dual antiplatelet therapy with clopidogrel and aspirin is standard post-percutaneous coronary intervention for coronary artery disease (CAD).
  • High on-treatment platelet reactivity (HPR) is linked to major adverse cardiac events, despite standard therapy.
  • Interindividual variability in response to clopidogrel and aspirin contributes to HPR.

Purpose of the Study:

  • Review current controversies and evidence regarding antiplatelet therapy effectiveness testing.
  • Examine genetic and phenotype-based laboratory tests for aspirin and clopidogrel response.
  • Correlate antiplatelet drug response testing with clinical outcomes.

Main Methods:

  • Literature review of studies on antiplatelet drug response testing.
  • Analysis of genetic and laboratory assays for clopidogrel and aspirin.
  • Evaluation of correlations between test results and clinical outcomes (ischemic events, bleeding).

Main Results:

  • No gold standard assay for antiplatelet drug response is established.
  • Variability in patient response to antiplatelet drugs is a significant factor.
  • Testing may identify patients at risk for recurrent ischemic events or bleeding.

Conclusions:

  • Antiplatelet therapy effectiveness testing should be considered case-by-case, particularly for acute coronary syndrome or stent thrombosis.
  • For stable CAD, targeted testing in specific risk groups may optimize treatment and reduce complications.
  • Cost-effectiveness and clinical utility guide decisions on routine testing.

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