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Vasculitis damage index in Behçet's disease
Fatema T Elgengehy1, Sherif M Gamal2, Nesreen Sobhy2
1Rheumatology and Rehabilitation Department, Cairo University, Cairo, Egypt. fatematalaat1980@yahoo.com.
Insights
The Vasculitis Damage Index (VDI) correlates with key clinical features and comorbidities in Behçet's disease (BD). This suggests VDI can help assess damage in BD patients, though a BD-specific index may be needed.
Area of Science:
- Rheumatology
- Clinical Medicine
- Systemic Vasculitis
Background:
- Behçet's disease (BD) is a systemic vasculitis.
- The Vasculitis Damage Index (VDI) is a validated tool for assessing damage in systemic vasculitis.
Purpose of the Study:
- To investigate the relationship between VDI and clinical manifestations in BD patients.
- To determine if VDI can be utilized to assess disease damage in Behçet's disease.
Main Methods:
- 109 BD patients were recruited for history taking, clinical examination, and lab tests.
- Disease activity was assessed using the BD current activity form.
- VDI was calculated, and statistical tests (Mann-Whitney, Kruskal Wallis, Spearman) were used to analyze data.
Main Results:
- VDI showed significant associations with neurological manifestations, uveitis, avascular necrosis, osteoporosis, impaired vision, and cataracts.
- VDI correlated with age, disease duration, and duration of eye involvement.
- Immunosuppressive treatments, including cyclophosphamide and biological agents, were significantly associated with VDI.
Conclusions:
- VDI is significantly associated with several key disease parameters in Behçet's disease.
- VDI may serve as a useful tool for damage assessment in BD.
- Further research is recommended to develop a BD-specific damage index.
Background:
Vasculitis damage index (VDI) is a validated damage index for systemic vasculitis, and as Behçet's disease is considered one of systemic vascular disease we aimed to study the relationship of the vasculitis damage index to clinical manifestations and comorbidity in patients with Behçet's disease (BD) to determine if VDI could be used to assess damage in patients with BD.
Methods:
A total of 109 patients with BD were recruited from the Rheumatology Department (outpatient and inpatient clinic), Cairo University Hospitals. All patients were subjected to full history taking, clinical examination, and routine laboratory investigations. Disease activity was assessed by the BD current activity form, and the VDI was calculated in all patients. The relationship of the VDI to the disease clinical manifestations was studied. Mann-Whitney and Kruskal Wallis tests were used to estimate differences in quantitative variables. Spearman correlation test was used to test for correlation between quantitative variables.
Results:
In the current study, the VDI ranged from 1 to 10, with a mean of 3.5 ± 1.8. It was significantly associated with total thrombosis (P = 0.022); total neurological manifestations (P = 0.000), especially stroke and cranial nerve affection; uveitis (P = 0.005); avascular necrosis (AVN) (P = 0.015); osteoporosis (P = 0.01); impaired vision (P < 0.0001); cataract (P < 0.0001); and diabetes (P = 0.012). Generally, immunosuppressive treatment was significantly associated with VDI (P = 0.039), especially cyclophosphamide (P < 0.0001), biological agent (P = 0.008), chlorambucil (P = 0.003), and anticoagulant (P = 0.02). VDI was also significantly correlated with age (P = 0.033), disease duration (P = 0.029), and duration of eye involvement (P = 0.003).
Conclusion:
VDI is significantly associated with most disease parameters of BD, except for parameters such as mucocutaneous manifestations and uncomplicated venous thrombosis; however, further studies may be needed to establish BD-specific damage index.
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