Hereditary cerebral hemorrhage with amyloidosis-Dutch type: a study of fibrinolysis

Thromb Haemost. 1992 Jan 23;67(1):16-8.

Abstract

In view of reported associations between increased bleeding tendency and systemically decreased alpha 2-antiplasmin in patients with systemic amyloid deposition we studied alpha 2-antiplasmin, fibrinogen, C-reactive protein and blood levels of locally produced endothelial hemostasis factors in the acute and quiescent phase in 16 patients with hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D). None of the factors measured in the quiescent phase of the disease was abnormal. In the acute phase, shortly after a stroke, only factor VIII:Ag was evidently elevated. We concluded that systemic abnormalities in the part of the fibrinolysis system studied are not likely to be responsible for multifocal and recurrent cerebral hemorrhages in HCHWA-D. The role of an elevated factor VIII:Ag level in the acute phase is unclear.

MeSH terms

  • Amyloidosis / blood
  • Amyloidosis / complications
  • Amyloidosis / genetics*
  • C-Reactive Protein / metabolism
  • Cerebral Hemorrhage / blood
  • Cerebral Hemorrhage / complications
  • Cerebral Hemorrhage / genetics*
  • Factor VIII / metabolism
  • Female
  • Fibrinogen / metabolism
  • Fibrinolysis*
  • Humans
  • Male
  • Middle Aged
  • alpha-2-Antiplasmin / metabolism

Substances

  • alpha-2-Antiplasmin
  • Factor VIII
  • Fibrinogen
  • C-Reactive Protein