Thrombin generation in patients with thrombotic thrombocytopenic purpura

Am J Hematol. 1989 Dec;32(4):255-7. doi: 10.1002/ajh.2830320404.

Abstract

Thrombotic thrombocytopenic purpura (TTP) is thought to be caused primarily by endothelial cell injury or primary platelet agglutination. A coagulation screen usually shows normal or minimal changes, but a modest elevation of fibrinogen/fibrin degradation products (FDP) is observed in many patients with TTP. To assess the thrombin generation in vivo in TTP, plasma levels of thrombin-antithrombin III complex (TAT) were measured together with plasmin-alpha 2-antiplasmin complex (PAP) in ten patients with acute TTP. Plasma TAT [mean 6.7 +/- (SD) 3.7 micrograms/liter] as well as PAP (2.1 +/- 1.2 mg/liter) were elevated in patients with TTP as compared with healthy subjects (TAT of 1.7 +/- 0.3 microgram/liter and PAP of 0.2 +/- 0.1 mg/liter; n = 10). These findings indicate that considerable amounts of thrombin and plasmin are actually generated in TTP, although the majority of patients do not show signs of consumption coagulopathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antifibrinolytic Agents*
  • Antithrombin III / metabolism
  • Female
  • Fibrinolysin / metabolism
  • Humans
  • Male
  • Middle Aged
  • Peptide Hydrolases / metabolism
  • Purpura, Thrombotic Thrombocytopenic / blood*
  • Thrombin / metabolism*
  • alpha-2-Antiplasmin / metabolism

Substances

  • Antifibrinolytic Agents
  • alpha-2-Antiplasmin
  • antithrombin III-protease complex
  • plasmin-plasmin inhibitor complex
  • Antithrombin III
  • Peptide Hydrolases
  • Thrombin
  • Fibrinolysin