The effect of genetic variants in the thrombin activatable fibrinolysis inhibitor (TAFI) gene on TAFI-antigen levels, clot lysis time and the risk of venous thrombosis

Br J Haematol. 2006 Jul;134(1):92-4. doi: 10.1111/j.1365-2141.2006.06117.x.

Abstract

Thrombin activatable fibrinolysis inhibitor (TAFI) is an important inhibitor of fibrinolysis. High TAFI antigen levels are associated with an increased risk of deep venous thrombosis (DVT). Because TAFI levels are partly determined genetically, we assessed the association between three TAFI gene polymorphisms (-438 G/A, 505 A/G and 1040 C/T), TAFI antigen levels and clot lysis times and the risk of DVT. Carriers of the 505G allele, which is associated with lower TAFI antigen levels than the 505A allele, showed an increased risk of DVT. This indicates that the relationship between TAFI and venous thrombosis is more complex than previously suggested.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Autoantigens / blood*
  • Blood Coagulation Tests
  • Carboxypeptidase B2 / genetics*
  • Female
  • Fibrinolysis
  • Genetic Predisposition to Disease
  • Heterozygote
  • Homozygote
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Risk
  • Venous Thrombosis / blood*
  • Venous Thrombosis / genetics*

Substances

  • Autoantigens
  • Carboxypeptidase B2