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Published on: February 10, 2023
Thrombophilia differences in cerebral venous sinus and lower extremity deep venous thrombosis
E M Wysokinska1, W E Wysokinski, R D Brown
1Division of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Insights
Thrombophilia testing reveals distinct differences in clotting factors between cerebral venous sinus thrombosis (CVST) and deep vein thrombosis (DVT) patients. These variations may explain why venous thrombosis occurs in different locations.
Area of Science:
- Medical research
- Hematology
- Vascular medicine
Background:
- Cerebral venous sinus thrombosis (CVST) and deep vein thrombosis (DVT) are serious conditions.
- Understanding the underlying causes, particularly thrombophilia, is crucial for diagnosis and treatment.
- Previous studies have not extensively compared thrombophilic variables across these distinct venous thrombosis types.
Purpose of the Study:
- To compare the prevalence of thrombophilic variables in patients with CVST versus those with lower extremity DVT.
- To identify potential differences in risk factors that may influence the location of venous thrombosis.
Main Methods:
- An inception cohort of 163 patients with first-time CVST (1995-2005) underwent comprehensive thrombophilia testing.
- Test results were compared to a randomly selected group of patients with lower extremity DVT who also had comprehensive thrombophilia testing.
Main Results:
- Thrombophilia was present in 29% of CVST patients.
- Prothrombin G20210A mutation was significantly more common in CVST patients (11%) compared to DVT patients.
- Factor V Leiden and protein C deficiency were more prevalent in DVT patients.
Conclusions:
- The prevalence of specific thrombophilic factors differs between CVST and DVT.
- These observed differences may provide insights into the mechanisms driving the geographic distribution of venous thrombosis.
Objective:
To characterize differences in the prevalence of thrombophilic variables in a large cohort of patients with cerebral venous sinus thrombosis (CVST) and lower extremity deep vein thrombosis (DVT).
Methods:
An inception cohort of individuals was identified with first lifetime incident CVST between 1995 and 2005 for whom comprehensive thrombophilia testing was available. To test the hypothesis that thrombophilia prevalence differs with respect to thrombus location, test results were compared to a randomly selected group of patients with lower extremity DVT with comprehensive thrombophilia testing.
Results:
During this time period, 163 patients with CVST were identified who underwent comprehensive thrombophilia testing. Thrombophilia results were abnormal in 29% including anticardiolipin antibodies (17%), heterozygous factor V Leiden (10%), and heterozygous prothrombin G20210A mutation (n = 14/122; 11%). The prothrombin mutation was more than twice as common in patients with CVST (p = 0.04). Activated protein C resistance, factor V Leiden, and protein C deficiency were more common in patients with DVT (p < 0.05 for each comparison). The anticardiolipin antibodies in patients with CVST were primarily low titer IgM isotype.
Conclusion:
The prevalence of selected thrombophilia factors differs comparing patients with cerebral venous sinus thrombosis and deep vein thrombosis. These differences may offer insights into mechanisms governing the geographic distribution of venous thrombosis.
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