Increased rate of factor V Leiden mutation in patients with cerebral venous thrombosis

J Neurol. 1998 Mar;245(3):149-52. doi: 10.1007/s004150050195.

Abstract

We investigated the association between cerebral venous thrombosis and hereditary resistance to activated protein C (APC) in 12 consecutive German patients with non-fatal cerebral venous thrombosis and in 187 controls without a history of thrombotic disorder. Three patients (25%) had a mutation in the factor V Leiden gene against only one subject in the control group. This difference was significant (P < 0.05), with an odds ratio of 11.7 (1.5-87; 95% confidence interval). Two patients carrying the mutation had additional common risk factors for thrombosis, and 2 had a positive family history of thromboembolism. We conclude that inherited APC resistance by a mutation in factor V Leiden is an important risk factor in non-fatal cerebral venous thrombosis. We recommend testing for APC resistance and, if abnormal for factor V Leiden mutation in patients with cerebral venous thrombosis.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Antithrombin III / analysis
  • Factor V / genetics*
  • Female
  • Germany
  • Humans
  • Intracranial Embolism and Thrombosis / blood
  • Intracranial Embolism and Thrombosis / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Protein C / analysis
  • Protein S / analysis
  • Retrospective Studies

Substances

  • Protein C
  • Protein S
  • Antithrombin III
  • Factor V