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Impact of initial clinical presentation on clopidogrel low response
Jean-Baptiste Landel1, Anne Bauters, Cédric Delhaye
1Unité des soins intensifs de cardiologie, centre hémodynamique, clinique de cardiologie, hôpital cardiologique, centre hospitalier régional et universitaire de Lille, boulevard du Pr-Jules-Leclercq, 59037 Lille cedex, France.
Insights
Acute coronary syndromes (ACS) significantly increase clopidogrel low response compared to stable coronary artery disease. This highlights the impact of initial clinical presentation on antiplatelet therapy effectiveness.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Clopidogrel response exhibits significant interindividual variability.
- Low clopidogrel response is linked to adverse outcomes post-percutaneous coronary intervention.
- Variability in clopidogrel response may also occur within individuals over time.
Purpose of the Study:
- To evaluate how initial clinical presentation affects clopidogrel low response.
- To compare clopidogrel response in patients with acute coronary syndromes versus stable coronary artery disease.
Main Methods:
- Prospective study of 100 patients, divided into acute coronary syndromes (ACS) and stable coronary artery disease groups.
- Clopidogrel response assessed 18-24 hours post-loading dose using VerifyNow-P2Y12 (platelet reaction units [PRUs]).
- Exclusion criteria included chronic clopidogrel therapy or use of specific other antiplatelet/anticoagulant agents.
Main Results:
- The ACS group showed significantly higher mean PRU values (197 ± 81) compared to the stable group (159 ± 94; p=0.03).
- Multivariable analysis identified the ACS presentation as a significant predictor of higher PRU values (p=0.02).
- Clopidogrel low responders (PRU > 230) were more frequent in the ACS group (38%) than in the stable group (18%; p=0.04).
Conclusions:
- Initial clinical presentation, particularly acute coronary syndromes (ACS), is a strong predictor of clopidogrel low response.
- Patient's evolving coronary artery disease influences clopidogrel response over time.
- Findings support more aggressive antiplatelet strategies for ACS patients, aligning with recent trial outcomes.
Background:
Large interindividual variability exists in clopidogrel response. Clopidogrel low response correlates with poor prognosis after percutaneous coronary intervention. Some authors also suggest intraindividual variability over time.
Aim:
To assess the impact of initial clinical presentation on clopidogrel low response.
Methods:
In this prospective study, clopidogrel response was assessed in 100 patients. Fifty patients presenting with acute coronary syndromes (ACS group) were compared with 50 patients with stable coronary artery disease matched 1:1 for age, sex, body mass index and diabetes (stable group). All patients were tested 18-24h after a 600 mg loading dose of clopidogrel using the VerifyNow-P2Y12 test (results expressed as platelet reaction units [PRUs]). Patients under chronic clopidogrel therapy or treated with glycoprotein IIb/IIIa inhibitors, bivalirudin or thrombolytics were excluded.
Results:
Mean age was 61 ± 12 years in each group; 28% of patients in each group were diabetic; mean body mass index was 27.6 ± 5.6 kg/m(2) in the ACS group and 27.9 ± 5.9 kg/m(2) in the stable group (p=0.80). Mean PRU values were 197 ± 81 in the ACS group and 159 ± 94 in the stable group (p=0.03). By multivariable analysis, the ACS group was significantly associated with a higher PRU value (p=0.02). There were significantly more clopidogrel low responders (PRU value>230) in the ACS group (38% vs. 18%; p=0.04).
Conclusion:
Our study confirms that initial clinical presentation, especially ACS, is a strong predictor of clopidogrel low response; this suggests that the evolution of coronary artery disease for one patient influences the clopidogrel response over time. These results are in accordance with recent trials showing a benefit for more aggressive antiplatelet therapy in ACS patients.
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