The factor VIII D1241E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levels

Thromb Haemost. 2005 Mar;93(3):453-6. doi: 10.1160/TH04-09-0629.


Elevated factor VIII (FVIII) levels are a recognized risk factor for venous thrombosis. Recently, family studies suggested that the G allele of the 3951C/G (D1241E) FVIII polymorphism is associated to lower FVIII activity. We investigated in case-control studies both biological effects (FVIII levels and activated protein C sensitivity ratio) and clinical associations (venous thromboembolism) of the D1241E change. Among 145 healthy and 150 thrombotic women, not carriers of known thrombophilic defects, the 1241E allele was associated with 11% reduced (t-test, P<0.05) FVIII levels. The effect on activated protein C sensitivity ratio was not statistically significant. Carriership of the 1241E allele, potentially conferring protection from thrombosis, was found in 22.8% of controls and in 15.3% of cases. In an additional cohort of factor V Leiden carriers (n=283), carriership of the 1241E allele was 25.2% among 143 asymptomatic subjects and 17.1% among 140 thrombotic patients. Our data do not indicate a specific interaction with factor V Leiden. These genotype distributions suggest a mild protective effect from venous thrombosis conferred by 1241E FVIII, masked by other genetic and/or environmental components, and detectable only in very large population studies. Our findings point toward the presence of genetic determinant of coagulation factor levels with a biologically significant role, but with a poor predictive value to estimate thrombotic risk beyond established risk factors.

MeSH terms

  • Activated Protein C Resistance*
  • Adult
  • Case-Control Studies
  • Factor V
  • Factor VII / genetics*
  • Factor VII / metabolism*
  • Female
  • Genotype
  • Humans
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Risk Assessment
  • Thromboembolism / etiology
  • Thromboembolism / genetics
  • Venous Thrombosis / etiology
  • Venous Thrombosis / genetics*


  • factor V Leiden
  • Factor V
  • Factor VII