Amyloid beta-protein precursor-rich platelet microparticles in thrombotic disease

Thromb Haemost. 1994 Oct;72(4):519-22.

Abstract

We investigated the association of amyloid beta-protein precursor (APP) and platelet derived microparticles in 20 normal controls and 91 patients with various diseases causing a thrombotic tendency. Compared with the controls, the mean percentage of APP-positive microparticles was significantly greater in the patients with cerebral infarction (39.1 +/- 17.7%, p < 0.001), diabetes (31.1 +/- 12.6%, p < 0.001), and uremia (30.1 +/- 14.7%, p < 0.01), but not in those with hypertension (8.2 +/- 6.3%, p = NS). Sixteen patients with cerebral infarction, 20 with diabetes, and 11 with uremia had microparticles with very high APP levels. In normal controls, 7.2 +/- 3.7% of the microparticles were positive for P-selectin, while the percentage in cerebral infarction, diabetes, uremia, and hypertension was respectively 43.5 +/- 15.1%, 40.0 +/- 12.8%, 31.8 +/- 12.2%, and 11.6 +/- 7.3%. There was a significant correlation between P-selectin and APP positivity of microparticles. Our results suggest that microparticle APP may have a regulatory influence on coagulation abnormalities.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Protein Precursor / blood*
  • Blood Platelets / chemistry*
  • Cerebral Infarction / blood*
  • Diabetes Complications
  • Diabetes Mellitus / blood*
  • Disease Susceptibility
  • Factor IXa / antagonists & inhibitors
  • Factor Xa Inhibitors
  • Humans
  • Hypertension / blood
  • Hypertension / complications
  • P-Selectin
  • Platelet Membrane Glycoproteins / blood
  • Thrombosis / blood*
  • Thrombosis / etiology
  • Uremia / blood*
  • Uremia / complications

Substances

  • Amyloid beta-Protein Precursor
  • Factor Xa Inhibitors
  • P-Selectin
  • Platelet Membrane Glycoproteins
  • Factor IXa