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Thrombosis in Behçet's disease: a retrospective survey from a single UK centre
Insights
Behçet's disease (BD) significantly increases thrombosis risk, particularly venous thrombosis, by 14-fold in Caucasian patients. Male BD patients face a sixfold higher risk of vein thrombosis and more severe vascular complications.
Area of Science:
- Rheumatology
- Vascular Medicine
- Immunology
Background:
- Behçet's disease (BD) is a rare multisystem inflammatory disorder.
- Vascular complications, including thrombosis, are a significant concern in BD.
- Understanding the prevalence and risk factors for thrombosis in BD is crucial for patient management.
Purpose of the Study:
- To investigate the prevalence and relative risk of vascular occlusion and thrombosis in Caucasian patients with Behçet's disease.
- To compare thrombosis rates between BD patients and a control group.
- To analyze gender-specific differences in thrombosis risk and associated symptoms in BD.
Main Methods:
- Retrospective cohort study involving 73 Caucasian patients with BD and 146 controls.
- Data collected from patients attending the Immunology/Rheumatology Department.
- Statistical analysis to determine the relative risk of thrombosis, adjusting for age and gender.
Main Results:
- Thrombosis was significantly more frequent in BD patients (32%) compared to controls (5%).
- Venous thrombosis was the predominant type, occurring in 25% of BD patients versus 3% of controls.
- BD conferred an 11-fold increased risk of any thrombosis and a 14-fold increased risk of venous thrombosis. Male BD patients had a 6-fold higher risk of vein thrombosis.
Conclusions:
- Behçet's disease significantly elevates the risk of venous thrombosis, with a 14-fold higher incidence in the studied Caucasian population.
- Male BD patients exhibit a substantially higher risk of vein thrombosis (sixfold) and are more prone to thrombophlebitis, folliculitis, and retinal vasculitis.
- These findings highlight the critical need for vigilant monitoring and management of vascular complications in patients with Behçet's disease, especially in males.
Objective:
To contribute to knowledge of vascular occlusion in Behçet's disease (BD), prevalence and relative risk for thrombosis were ascertained retrospectively in a cohort of Caucasian patients with the disease.
Patients:
The study included 73 BD patients (36 males, 37 females, mean age 45+/-11 yr) attending the Immunology/Rheumatology Department of Northwick Park Hospital. A group of 146 patients without BD, attending the same department, served as a control group.
Results:
Thrombosis was more frequent in BD patients than in controls (23/73, 32% vs 7/146, 5%, P<0.001). This was accounted for by a higher prevalence of venous thrombosis in BD patients (18/73, 25% vs 4/146, 3%, P<0.001). Gender-adjusted data revealed an 11-fold risk of developing any thrombosis and a 14-fold risk of developing venous thrombosis in BD. After adjusting for differences in age at first symptoms, male BD patients showed a 6-fold higher risk of vein thrombosis. Males reported more often thrombophlebitis (13/36, 36% vs 0/0, P<0.001), folliculitis (8/36, 22% vs 1/37, 3%, P<0.01) and retinal vasculitis (13/36, 36%, vs 4/37, 11%, P=0.01) than females, in whom arthralgia prevailed (23/37, 62%, vs 12/36, 33%, P=0.01).
Conclusion:
In our population, BD confers a 14-fold risk of developing venous thrombosis. The risk is sixfold higher in male BD patients, who fare worse than females with regard to thrombophlebitis, folliculitis and retinal vasculitis.
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