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Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Persistent high on-treatment platelet reactivity in acute coronary syndrome
Donald R Lynch1, Farooq H Khan, Dhananjay Vaidya
1Department of Medicine, Johns Hopkins Medical Institute, Johns Hopkins Bayview Medical Center, 4940 Eastern Avenue, 301 Building, Division of Cardiology, Baltimore, MD 21224, USA.
Insights
Patients with acute coronary syndrome (ACS) on aspirin therapy show persistent high platelet reactivity three months after treatment. This sustained platelet activity may increase the risk of future cardiovascular events.
Area of Science:
- Cardiology
- Hematology
- Pharmacology
Background:
- Persistent high on-treatment platelet reactivity is linked to adverse cardiovascular outcomes in acute coronary syndrome (ACS) patients.
- The temporal changes in platelet function following ACS and antiplatelet therapy are not well understood.
Purpose of the Study:
- To investigate platelet activity at a three-month follow-up in patients initially presenting with ACS.
- To assess the evolution of platelet reactivity under aspirin therapy in ACS patients.
Main Methods:
- 124 patients (65 ACS, 59 controls) were enrolled. 25 ACS patients underwent repeat platelet function testing at three months.
- Platelet aggregation induced by epinephrine (EPI) and adenosine diphosphate (ADP) was measured at baseline and follow-up.
- P-selectin and PAC-1 expression were monitored at both time points in ACS patients on aspirin therapy.
Main Results:
- ACS patients on aspirin showed no significant percentage change in EPI- and ADP-stimulated platelet aggregation at three months.
- No significant changes in PAC-1 or P-selectin expression were observed at the three-month follow-up.
- Platelet reactivity remained persistently high in ACS patients at three months post-presentation.
Conclusions:
- This study demonstrates persistent high on-treatment platelet reactivity in ACS patients at three months.
- Sustained high platelet reactivity may indicate an increased risk for recurrent cardiovascular events in these patients.
- Further research is needed to explore strategies to mitigate persistent platelet reactivity in ACS management.
Abstract:
Persistent high on-treatment platelet reactivity in acute coronary syndrome (ACS) patients managed with appropriate antiplatelet therapy has been correlated with increased risk of cardiovascular events; however, the evolution of this phenomenon overtime is not well known. We investigated platelet activity at a three month follow-up after initial presentation with an ACS. We enrolled a total of 124 patients in the study, 65 were diagnosed with ACS and 59 controls who presented with non-cardiac chest pain for baseline comparisons. Of the enrolled patients, we had 25 ACS patients return, in stable condition, three months after their initial presentation for repeat platelet functional testing. Epinephrine (EPI), adenosine diphosphate (ADP), and arachidonic acid induced platelet aggregation were monitored at baseline with repeat measurement of EPI- and ADP-stimulated aggregation at follow-up. In addition, P-selectin and PAC-1 expression were monitored at presentation and at a three month follow-up period. ACS patients were maintained on aspirin therapy during the intervening period. At the three month follow-up visit, ACS patients initiated on aspirin had no significant percentage change in aggregation to submaximal concentrations of EPI and ADP. They also had no significant percentage change in PAC-1 or P-selectin expression. This study demonstrates persistent high on-treatment platelet reactivity in ACS patients at a three month follow-up, which may place these patients at increased risk of recurrent cardiovascular events.
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