Immature Platelet Fraction Predicts Adverse Events in Patients With Acute Coronary Syndrome: the ISAR-REACT 5 Reticulated Platelet Substudy.
Veröffentlichungsart | Zeitschriften-/Journalbeitrag (peer-reviewed) |
|---|---|
Medien | Arterioscler Thromb Vasc Biol. |
Veröffentlichungsdatum | 2023-02-01 |
Band | 2023/43 |
Seiten | 83-93 |
DOI | |
Zitierung | Bongiovanni, Dario; Schreiner , Nina; Gosetti, Rosanna; Mayer, Katharina; Angiolillo, Dominick J; Sibbing, Dirk; Holdenrieder, Stefan; Anetsberger, Aida; von Scheidt, Moritz; Schunkert, Heribert; Laugwitz, Karl-Ludwig; Schüpke, Stefanie; Kastrati, Adnan; Fegers-Wustrow, Isabel; Bernlochner , Isabell (2023): Immature Platelet Fraction Predicts Adverse Events in Patients With Acute Coronary Syndrome: the ISAR-REACT 5 Reticulated Platelet Substudy.. Arterioscler Thromb Vasc Biol. 2023/43, 2, S. 83-93. DOI: 10.1161/ATVBAHA.122.318614 |
Peer Reviewed | Ja |
Autoren |
Dario Bongiovanni |
Immature Platelet Fraction Predicts Adverse Events in Patients With Acute Coronary Syndrome: the ISAR-REACT 5 Reticulated Platelet Substudy.
Abstract
Background: Immature or reticulated platelets are associated with impaired efficacy of antiplatelet drugs and adverse events in cardiovascular patients. Their role as a predictive biomarker in patients with acute coronary syndrome treated with potent P2Y12 receptor inhibitors is not fully understood. We aimed to prospectively evaluate reticulated platelets as a predictor of the primary end point of the ISAR-REACT 5 trial consisting of death, myocardial infarction, or stroke at 1 year in patients with acute coronary syndrome randomized to prasugrel or ticagrelor.
Methods: Immature platelet fraction (IPF) was assessed within 48 hours after randomization. Patients were divided based on the IPF median values: the IPFhigh group included patients with IPF>median and the IPFlow group included patients with IPF≤median. Platelet aggregation was assessed using the Multiplate Analyzer and was correlated to IPF.
Results: Five hundred seventy-seven patients were included in the study. IPF values in % (median [interquartile range]) within the first 48 hours did not differ between the two study groups: 3.6 (2.5-5.2)% in the prasugrel group and 3.6 (2.5-5.4)% in the ticagrelor group (P=0.882). The incidence of the primary end point was significantly higher in the IPFhigh (IPF>3.6%) group compared with the IPFlow (IPF≤3.6%) group: 13.0% versus 7.2% (HRadj, 1.74 [1.02-3.00]; P=0.044), independently from the assigned drug (Pint=0.159). No significant association between IPF and BARC 3 to 5 bleeding was observed. ADP-induced platelet aggregation correlated significantly with IPF in patients treated with prasugrel (r=0.22; P=0.005) while no correlation was detected in patients treated with ticagrelor (r=0.09; P=0.257).
Conclusions: Independently from drug treatment, IPF was associated with the primary end point and therefore is a promising biomarker for the prediction of adverse cardiovascular events in patients with acute coronary syndrome treated with prasugrel or ticagrelor.
Registration: www.
Clinicaltrials: gov; Unique identifier: NCT01944800.
Keywords: acute coronary syndrome; biomarker; cardiovascular events; drug; immature platelets; reticulated platelets.