P-Selectin expression, platelet aggregates, and platelet-derived microparticle formation are increased in peripheral arterial disease

• Published in: Blood coagulation & fibrinolysis Vol. 11; no. 8; p. 723
• Main Authors: Zeiger, F, Stephan, S, Hoheisel, G, Pfeiffer, D, Ruehlmann, C, Koksch, M
• Format: Journal Article
• Language: English
• Published: England 01.12.2000
• Subjects: Adult; Blood Platelets - pathology; Blood Platelets - physiology; Blood Platelets - ultrastructure; Cytoplasmic Granules - physiology; Cytoplasmic Granules - ultrastructure; Humans; Male; Middle Aged; P-Selectin - biosynthesis; Peripheral Vascular Diseases - blood; Peripheral Vascular Diseases - pathology; Peripheral Vascular Diseases - physiopathology; Platelet Aggregation; Platelet Count
• DOI: 10.1097/00001721-200012000-00005
• ISSN: 0957-5235

Platelet volume has been reported to be increased in vascular disease. Therefore, we studied the relationship of mean platelet volume and platelet count as well as flow cytometrically measured platelet size and platelet function in 50 patients with peripheral arterial disease and 50 healthy volunteers. Platelet activation was measured by P-selectin expression analysis on resting and on stimulated platelets, and the determination of platelet aggregates and platelet-derived microparticles using flow cytometry. P-Selectin expression on platelets was significantly elevated in patients suffering from peripheral arterial disease (all P<0.0001). Platelet aggregates (P<0.0001) and platelet-derived microparticles (P<0.0001) were significantly higher in the patient group compared with controls, whereas mean platelet volume and platelet count showed no significant differences. Platelet count was inversely related to mean platelet volume in patients and controls (r = -0.43, P<0.001). The present study supports the hypothesis of platelet hyperreactivity and circulating activated platelets in peripheral arterial disease. Mean platelet volume, and platelet count cannot be used as predictive markers for platelet activation in peripheral arterial disease patients.