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Updated: May 18, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Personalizing antiplatelet therapy with clopidogrel
1Universitäts-Herzzentrum Freiburg-Bad Krozingen, Klinik für Kardiologie und Angiologie II, Bad Krozingen, Germany. dietmar.trenk@universitaets-herzzentrum.de
Insights
Dual antiplatelet therapy with aspirin and clopidogrel is standard after coronary intervention. High on-clopidogrel platelet reactivity increases ischemic event risk, prompting strategies for personalized antiplatelet therapy.
Area of Science:
- Cardiology
- Pharmacology
- Genetics
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and clopidogrel is standard for preventing ischemic events post-percutaneous coronary intervention (PCI).
- Significant interindividual variability exists in patient response to clopidogrel, a key antiplatelet medication.
- Elevated on-clopidogrel platelet reactivity is linked to a higher risk of ischemic complications.
Purpose of the Study:
- To review factors influencing clopidogrel response variability.
- To discuss strategies for optimizing antiplatelet therapy effectiveness.
- To improve clinical outcomes in patients undergoing PCI and those with acute coronary syndromes (ACSs).
Main Methods:
- Literature review of clinical studies on clopidogrel therapy.
- Analysis of factors contributing to variable antiplatelet response.
- Discussion of platelet function testing and genotyping approaches.
Main Results:
- Identified clinical, demographic, and genetic factors affecting clopidogrel response.
- Demonstrated correlation between high on-clopidogrel platelet reactivity and increased ischemic risk.
- Highlighted potential for personalized medicine in antiplatelet therapy.
Conclusions:
- Tailoring antiplatelet therapy based on individual response can mitigate ischemic events.
- Platelet function testing and genotyping offer promising strategies for optimizing clopidogrel efficacy.
- Personalized antiplatelet strategies may improve clinical outcomes in high-risk cardiovascular patients.
Abstract:
Dual antiplatelet therapy with aspirin and clopidogrel is the accepted standard for prevention of ischemic complications after percutaneous coronary intervention and has been shown to reduce cardiovascular events in patients with acute coronary syndromes (ACSs). There is substantial interindividual variability in antiplatelet response to clopidogrel. Various clinical studies have demonstrated that patients with high on-clopidogrel platelet reactivity incur an increased risk for ischemic events. In recent years, several clinical and demographic variables as well as multiple genetic factors contributing to the variability in antiplatelet response to clopidogrel have been identified. We discuss strategies based on platelet function testing or genotyping for improvement of antiplatelet effects of clopidogrel and thereby clinical outcome.
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