Thromb Haemost 2016; 116(05): 941-948
DOI: 10.1160/TH16-03-0191
Cellular Haemostasis and Platelets
Schattauer GmbH

Impact of reticulated platelets on antiplatelet response to thienopyridines is independent of platelet turnover

Christian Stratz
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Thomas Nührenberg
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Michael Amann
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Marco Cederqvist
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Pascal Kleiner
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Christian M. Valina
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Dietmar Trenk
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Franz-Josef Neumann
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
,
Willibald Hochholzer
1   University Heart Center Freiburg – Bad Krozingen, Department of Cardiology and Angiology II, Bad Krozingen, Germany
› Author Affiliations

Financial support: This trial was supported by the German Heart Foundation/German Foundation of Heart Research and the University Heart Center Freiburg · Bad Krozingen.
Further Information

Publication History

Received: 07 March 2016

Accepted after major revision: 11 July 2016

Publication Date:
30 November 2017 (online)

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Summary

Reticulated platelets are associated with impaired antiplatelet response to thienopyridines. It is uncertain whether this interaction is caused by a decreased drug exposure due to high platelet turnover reflected by elevated levels of reticulated platelets or by intrinsic properties of reticulated platelets. This study sought to investigate if the impact of reticulated platelets on early antiplatelet response to thienopyridines is mainly caused by platelet turnover as previously suggested. Elective patients undergoing coronary intervention were randomised to loading with clopidogrel 600 mg or prasugrel 60 mg (n=200). Adenosine diphosphate (ADP)-induced platelet reactivity was determined by impedance aggregometry before, at 30, 60, 90, and 120 minutes and at day 1 after loading. Immature platelet count was assessed as marker of reticulated platelets by flow cytometry. Platelet reactivity increased with rising levels of immature platelet count in both groups. This effect was more distinctive in patients on clopidogrel as compared to patients on prasugrel. Overall, immature platelet count correlated well with on-treatment platelet reactivity at all timepoints (p < 0.001). These correlations did not change over time in the entire cohort as well as in patients treated with clopidogrel or prasugrel indicating an effect independent of platelet turnover (comparison of correlations 120 minutes/day 1: p = 0.64). In conclusion, the association of immature platelet count with impaired antiplatelet response to thienopyridines is similar early and late after loading. This finding suggests as main underlying mechanism another effect of reticulated platelets on thienopyridines than platelet turnover.

Supplementary Material to this article is available online at www.thrombosis-online.com.