Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke

Atrial fibrillation (AF) increases the risk of ischemic stroke (IS). We hypothesized that the functional form of platelet receptor glycoprotein (GP) VI, GPVI-dimer, which binds to collagen and fibrin causing platelet activation, is overexpressed in patients with AF who have not had a stroke.  A tota...

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Veröffentlicht in:TH open : companion journal to thrombosis and haemostasis 2023-10, Vol.7 (4), p.e294-e302
Hauptverfasser: Induruwa, Isuru, Kempster, Carly, Thomas, Patrick, McKinney, Harriet, Malcor, Jean-Daniel, Bonna, Arkadiusz, Batista, Joana, Soejima, Kenji, Ouwehand, Willem, Farndale, Richard W, Downes, Kate, Moroi, Masaaki, Jung, Stephanie M, Warburton, Elizabeth A
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Sprache:eng
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Zusammenfassung:Atrial fibrillation (AF) increases the risk of ischemic stroke (IS). We hypothesized that the functional form of platelet receptor glycoprotein (GP) VI, GPVI-dimer, which binds to collagen and fibrin causing platelet activation, is overexpressed in patients with AF who have not had a stroke.  A total of 75 inpatients with AF were recruited. None were admitted with or had previously had thrombotic events, including IS or myocardial infarction. Platelet surface expression of total GPVI, GPVI-dimer, and the platelet activation marker P-selectin were quantitated by whole blood flow cytometry. Serum biomarkers were collected in AF patients. Results were compared against patients contemporaneously admitted to hospital with similar age and vascular risk-factor profiles without AF (noAF,  = 30).  Patients with AF have similar total GPVI surface expression (  = 0.58) and P-selectin exposure (  = 0.73) on their platelets compared with noAF patients but demonstrate significantly higher GPVI-dimer expression (  = 0.02 Patients with paroxysmal AF express similar GPVI-dimer levels compared with permanent AF and GPVI-dimer levels were not different between anticoagulated groups. Serum N-terminal pro b-type natriuretic peptide (  
ISSN:2512-9465
2567-3459
2512-9465
DOI:10.1055/s-0043-1776328