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Updated: Jun 16, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Variability of residual platelet function despite clopidogrel treatment in patients with peripheral arterial
Birgit Linnemann1, Jan Schwonberg, Stefan W Toennes
1Division of Vascular Medicine, Department of Internal Medicine, J.W. Goethe University Hospital, Frankfurt/Main, Germany. Birgit.Linnemann@kgu.de
Insights
Clopidogrel non-responsiveness in peripheral arterial occlusive disease patients is not stable over time. This variability in platelet function may not solely be due to patient compliance.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Residual platelet activity despite clopidogrel treatment can indicate poor cardiovascular outcomes.
- Most research focuses on clopidogrel combined with aspirin in percutaneous coronary intervention patients.
Purpose of the Study:
- To evaluate clopidogrel's antiplatelet effect in peripheral arterial occlusive disease (PAOD) patients without aspirin.
- To determine the reproducibility of clopidogrel non-responsiveness during long-term follow-up.
Main Methods:
- Fifty-four stable PAOD patients received 75 mg/d clopidogrel.
- Platelet function assessed via light transmittance aggregometry (LTA) with ADP.
- Clopidogrel and metabolite levels measured using HPLC-coupled mass spectrometry.
Main Results:
- 35.2% baseline and 17.6% follow-up patients showed residual platelet function (>43% aggregation).
- 26.5% of patients switched between responder and non-responder status.
- Clopidogrel or metabolite detected in 89.5% (baseline) and 83.3% (follow-up) of non-responders.
Conclusions:
- Non-responsiveness to clopidogrel, measured by ADP-induced LTA, is not consistently stable.
- The observed variability in platelet response is not solely attributable to non-compliance.
Abstract:
Residual platelet function despite treatment with clopidogrel may predict an unfavourable cardiovascular outcome. The majority of studies have investigated the effects of clopidogrel administration in conjunction with aspirin in patients undergoing percutaneous coronary intervention. The primary objective of the present study was to assess the platelet response to clopidogrel in the absence of aspirin in patients with peripheral arterial occlusive disease (PAOD) and to investigate whether non-responsiveness to clopidogrel is reproducible during long-term follow-up. Fifty-four clinically stable PAOD patients on a maintenance dose of 75 mg/d clopidogrel were enrolled in this study. Platelet function was assessed at baseline and after a median follow-up of 18 months using light transmittance aggregometry (LTA) with 2 microM ADP as an agonist. HPLC-coupled mass spectrometry was used to detect clopidogrel and clopidogrel carboxylic acid, the main metabolite of clopidogrel. Residual platelet function, as defined by late aggregation values within the reference range (i.e., >43%), was observed in 35.2% of patients at baseline and 17.6% during follow-up. During the observation period, 26.5% had switched from responder to non-responder status or vice versa. Among non-responders, either clopidogrel or its metabolite was detected in 89.5% and 83.3% of patients at baseline and at follow-up, respectively. We conclude that non-responsiveness to clopidogrel as determined by ADP-induced LTA is not stable over time. This phenomenon cannot be attributed to non-compliance alone.
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