Hereditary protein S deficiency in young adults with arterial occlusive disease

Thromb Haemost. 1990 Oct 22;64(2):206-10.

Abstract

Protein S is the vitamin K dependent cofactor of activated protein C. It has an important role in the regulation of blood coagulation and fibrinolysis. Hereditary protein S deficiency is associated with familial venous thrombophilia. Since a few patients with arterial occlusions have been reported to be protein S deficient, it is speculated that hereditary protein S deficiency may be also a risk factor for the development of arterial thrombosis. In a group of 37 consecutive patients with arterial occlusive disease presenting before the age of 45, three patients were found heterozygous for hereditary protein S deficiency. None of the patients had a protein C deficiency or an antithrombin III deficiency. Family investigations showed a clear association between the hereditary deficiency and venous thrombosis, but a relation between the deficiency and arterial thrombosis was less obvious. A review of previous literature on patients with arterial thrombosis and protein S deficiency revealed that more extensive studies are needed to demonstrate whether or not hereditary protein S deficiency is a risk factor for the development of arterial thrombosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Arterial Occlusive Diseases / blood
  • Arterial Occlusive Diseases / genetics*
  • Female
  • Glycoproteins / deficiency*
  • Glycoproteins / genetics
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Protein S

Substances

  • Glycoproteins
  • Protein S