Tissue factor and thrombin in sickle cell anemia

Thromb Res. 2012 May;129 Suppl 2(Suppl 2):S70-2. doi: 10.1016/j.thromres.2012.02.038. Epub 2012 Mar 6.

Abstract

Sickle cell anemia is an inherited hematologic disorder associated with hemolytic and vaso-occlusive complications. An activation of coagulation is also a prominent feature of sickle cell anemia. Growing evidence indicates that coagulation may contribute to the inflammation and vascular injury in sickle cell anemia. This review focuses on tissue factor expression and its contribution to the activation of coagulation, thrombosis and vascular inflammation in sickle cell anemia.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Anemia, Sickle Cell / blood*
  • Animals
  • Humans
  • Thrombin / metabolism*
  • Thromboplastin / metabolism*

Substances

  • Thromboplastin
  • Thrombin