Platelet Function and Maturity and Related microRNA Expression in Whole Blood in Patients with ST-Segment Elevation Myocardial Infarction

Author:

Pedersen Oliver Buchhave123ORCID,Hvas Anne-Mette4,Pasalic Leonardo56,Kristensen Steen Dalby23,Grove Erik Lerkevang23ORCID,Nissen Peter H.13

Affiliation:

1. Thrombosis and Haemostasis Research Unit, Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark

2. Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark

3. Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark

4. Faculty of Health, Aarhus University, Aarhus, Denmark

5. Institute of Clinical Pathology and Medical Research, Westmead Hospital, NSW Health Pathology, Sydney, Australia

6. Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia

Abstract

Background Reduced effect of antiplatelet therapy has been reported in patients with ST-segment elevation myocardial infarction (STEMI). MicroRNAs (miRs) may influence platelet function and maturity, and subsequently the effect of antiplatelet therapy. Objectives We aimed to explore the association between miR expression and platelet function and maturity in patients with acute STEMI and healthy individuals. Methods We performed an observational study of STEMI patients admitted directly to primary percutaneous coronary intervention. Patients were treated with antiplatelet therapy according to guidelines. Within 24 hours after admission, blood samples were obtained to measure: the expression of 10 candidate miRs, platelet function markers using advanced flow cytometry, platelet aggregation, serum thromboxane B2, and platelet maturity markers. Furthermore, blood samples from healthy individuals were obtained to determine the normal variation. Results In total, 61 STEMI patients and 50 healthy individuals were included. STEMI patients had higher expression of miR-21–5p, miR-26b-5p, and miR-223–3p and lower expression of miR-150–5p, miR423–5p, and miR-1180–3p than healthy individuals. In STEMI patients, the expression of miR-26b-5p showed the most consistent association with platelet function (all p-values <0.05, Spearman's rho ranging from 0.27 to 0.41), while the expression of miR-150–5p and miR-223–3p showed negative associations with platelet function. No association between miR expression and platelet maturity markers was observed. Conclusion In patients with STEMI, the expression of six miRs was significantly different from healthy individuals. The expression of miR-26b-5p may affect platelet function in acute STEMI patients and potentially influence the effect of antiplatelet therapy.

Funder

Department of Clinical Biochemistry

Aarhus University Hospital, Denmark

Snedkermester Sophus Jacobsen and hustru Astrid Jacobsens Foundation

Murermester Lauritz Peter Christensen og hustru Kirsten Sigrid Christensens Foundation

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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