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Updated: Jun 24, 2026

Dynamic Multiparameter Platelet Function Assessment Using a Capacitive Biosensor
Published on: May 2, 2025
Antiplatelet drug 'resistance'. Part 1: mechanisms and clinical measurements
Joseph M Sweeny1, Diana A Gorog, Valentin Fuster
1Mount Sinai Medical Center, One Gustave L Levy Place, New York, NY 10029, USA.
Insights
Patients with cardiovascular disease on antiplatelet therapy can experience poor outcomes due to nonresponsiveness. Further research is needed to understand and overcome this reduced effectiveness of antiplatelet drugs.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Clinical Trials
Background:
- Antiplatelet drug therapy is crucial for managing cardiovascular disease and coronary artery disease.
- Despite benefits, many patients experience recurrent adverse cardiovascular events due to nonresponsiveness to antiplatelet agents.
- Variability in responsiveness is linked to pharmacological and pharmacokinetic factors, including genetics and drug interactions.
Purpose of the Study:
- To review the current understanding of antiplatelet drug nonresponsiveness in cardiovascular disease.
- To highlight the association between nonresponsiveness and adverse clinical outcomes.
- To identify the need for further research and standardized trials to establish effective therapeutic strategies.
Main Methods:
- Review of large clinical trials and observational studies on antiplatelet therapy.
- Analysis of factors contributing to variability in antiplatelet drug responsiveness.
- Examination of recent randomized clinical trials investigating dosing strategies.
Main Results:
- Observational studies consistently link antiplatelet drug nonresponsiveness to adverse clinical outcomes.
- Recent randomized trials suggest increased antiplatelet drug dosing may reduce adverse events.
- Limitations in existing studies include varied dosing, laboratory assessments, and interindividual responses.
Conclusions:
- Antiplatelet drug nonresponsiveness remains a significant clinical challenge in cardiovascular disease management.
- Standardized, large-scale clinical trials are essential to confirm the link between nonresponsiveness and outcomes.
- Developing strategies to overcome blunted antiplatelet effects is critical for improving patient care.
Abstract:
Antiplatelet drug therapy has become one of the cornerstones of treatment for patients with cardiovascular disease. Large clinical trials have shown that antiplatelet medications have important clinical benefits and prevent adverse outcomes in patients with coronary artery disease. Recurrent adverse cardiovascular events still occur in a substantial proportion of patients on standard dual antiplatelet therapy, however, which has been attributed to nonresponsiveness to this treatment. Both pharmacological and pharmacokinetic mechanisms are involved in variability in responsiveness to antiplatelet agents, and include drug bioavailability, medication noncompliance, drug-drug interactions, cytochrome P450 activity, and genetic polymorphisms. Numerous observational studies have consistently shown an association between antiplatelet drug nonresponsiveness and adverse clinical outcomes. However, these studies are limited by varying antiplatelet drug dosing regimens, heterogeneous laboratory assessments for ex vivo platelet function, and wide interindividual variation in platelet responses. Only within the last 2 years have randomized clinical trials indicated that increased dosing with antiplatelet drugs could reduce adverse clinical outcomes. Nonetheless, large clinical trials with standardized laboratory methods and well-defined protocols are needed that will definitively determine the association between antiplatelet drug nonresponsiveness and clinical events, and establish therapeutic strategies to overcome blunted antiplatelet effects.
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