IS PLATELET PHOSPHOLIPID-DEPENDENT THROMBIN GENERATION ALTERED BY ACUTE MYOCARDIAL-INFARCTION OR ASPIRIN

Citation
S. Rota et al., IS PLATELET PHOSPHOLIPID-DEPENDENT THROMBIN GENERATION ALTERED BY ACUTE MYOCARDIAL-INFARCTION OR ASPIRIN, Thrombosis research, 83(4), 1996, pp. 329-338
Citations number
23
Categorie Soggetti
Hematology,"Cardiac & Cardiovascular System","Peripheal Vascular Diseas
Journal title
ISSN journal
00493848
Volume
83
Issue
4
Year of publication
1996
Pages
329 - 338
Database
ISI
SICI code
0049-3848(1996)83:4<329:IPPTGA>2.0.ZU;2-C
Abstract
The ability of unactivated and calcium ionophore activated platelets t o support thrombin generation in defibrinated plasma was measured by a chromogenic substrate assay in the absence of clot formation. Platele t phospholipid-dependent thrombin generation (Platelet-TG) could be me asured using platelets isolated from blood collected into either sodiu m citrate or EDTA as anticoagulant. Measurements were stable in sample s kept at room temperature for 24 hours after venesection. There was n o significant difference in either the unactivated or activated platel et-TG with platelets collected into either anticoagulant (mean differe nce 10.12 nmol/min unactivated and 10.60 nmol/min activated). There wa s no correlation between unactivated and activated platelet-TG and pat ient age. Platelet-TG was 179 (153-237) nmol/min (median and inter-qua rtile range) for unactivated and 489 (462-508) nmol/min for activated platelets from healthy volunteer subjects (median age 31, range 20-40 years). Platelet-TG was the same in subjects from a population-based c ohort study (median age 58, range 45-70 years [162 (142-193) nmol/min and 527 (490-551) nmol/min, unactivated and activated platelets respec tively] as compared to patients admitted with acute myocardial infarct ion (median age 68, range 36-85 years [179 (146-200) nmol/min and 473 (440-517) nmol/min unactivated and activated platelets respectively] ( p=0.497 for comparison between unactivated platelet-TGs and p=0.487 fo r comparison between activated platelet-TGs in the two groups). Aspiri n inhibited platelet aggregation but did not affect platelet-TG using either unactivated or activated platelets exposed to aspirin in vitro; or in vivo, using platelets obtained from individuals after ingestion of aspirin. In conclusion these results show that for measurement of platelet -TG, blood samples can be anticoagulated with EDTA as well as sodium citrate for up to 24 hours after venesection and that this mea surement is not affected by subject age, aspirin treatment or the acut e stage of myocardial infarction.