Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area

Dig Liver Dis. 2001 Oct;33(7):559-62. doi: 10.1016/s1590-8658(01)80107-9.

Abstract

Background: Thromboembolism has been reported to be associated with inflammatory bowel disease.

Aim: To evaluate the association of factor V Leiden and prothrombin gene mutation with inflammatory bowel disease in a population of patients with thromboembolic events and inflammatory bowel disease and in a control population of patients with inflammatory bowel disease without thromboembolic events.

Patients and methods: A series of 18 patients with inflammatory bowel disease and a history of arterial or venous thrombosis and 45 patients with inflammatory bowel disease without thromboembolic events were evaluated for the presence of factor V Leiden and prothrombin gene mutation. Frequency of gene mutation was compared with its occurrence in 100 healthy controls.

Results: One patient with inflammatory bowel disease without thromboembolic events was heterozygous for factor V Leiden mutation. whereas no patient with a thromboembolic event had factor V Leiden mutation. No patients (either cases or controls) had prothrombin gene mutation. In the healthy population the frequency of factor V Leiden and prothrombin mutation was 5% and 2%, respectively.

Conclusions: Data emerging from the present study do not support any role of factor V Leiden and prothrombin gene mutation as the cause of thromboembolism in inflammatory bowel disease.

MeSH terms

  • Colitis, Ulcerative / blood
  • Colitis, Ulcerative / genetics*
  • Crohn Disease / blood
  • Crohn Disease / genetics*
  • Factor V / genetics*
  • Female
  • Humans
  • Male
  • Mediterranean Region
  • Middle Aged
  • Point Mutation*
  • Prevalence
  • Prothrombin / genetics
  • Thromboembolism / blood
  • Thromboembolism / genetics*

Substances

  • factor V Leiden
  • Factor V
  • Prothrombin