ADAMTS-13 assays in thrombotic thrombocytopenic purpura

J Thromb Haemost. 2010 Apr;8(4):631-40. doi: 10.1111/j.1538-7836.2010.03761.x. Epub 2010 Jan 21.

Abstract

ADAMTS-13, the thirteenth member of the ADAMTS (A Disintegrin And Metalloprotease with Thrombo-Spondin 1 repeats) family, is the plasma metalloprotease responsible for regulating the multimeric structure of VWF. In congenital or acquired deficiency it is actively involved in the pathophysiology of thrombotic thrombocytopenic purpura (TTP), a rare but life threatening disease characterized by microangiopathic haemolytic anaemia and consumptive thrombocytopenia leading to disseminated microvascular thrombosis and variable signs and symptoms of organ ischemia and damage. In the last few years, a number of in house and commercial laboratory assays for ADAMTS-13 and its autoantibodies have been developed. The features and clinical utility of ADAMTS-13 assays are summarized in this review.

Publication types

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

MeSH terms

  • ADAM Proteins / blood*
  • ADAM Proteins / deficiency
  • ADAM Proteins / genetics
  • ADAM Proteins / immunology
  • ADAMTS13 Protein
  • Autoantibodies / blood
  • Biomarkers / blood
  • Clinical Enzyme Tests* / standards
  • Diagnosis, Differential
  • Humans
  • Immunoassay* / standards
  • Predictive Value of Tests
  • Purpura, Thrombotic Thrombocytopenic / diagnosis*
  • Purpura, Thrombotic Thrombocytopenic / enzymology
  • Purpura, Thrombotic Thrombocytopenic / genetics
  • Purpura, Thrombotic Thrombocytopenic / immunology
  • Reagent Kits, Diagnostic

Substances

  • Autoantibodies
  • Biomarkers
  • Reagent Kits, Diagnostic
  • ADAM Proteins
  • ADAMTS13 Protein
  • ADAMTS13 protein, human