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Comorbid Inflammatory Diseases in Behçet's Disease: A Multicenter Large Cohort Study
Emine Büşra Ata1, İbrahim Yahya Çakır2, Semiha Köroğlu3
1Department of Internal Medicine, Division of Rheumatology, University of Health Sciences, Gulhane Training and Research Hospital, Ankara, Turkiye.
Insights
Behçet
Area of Science:
- Rheumatology
- Immunology
- Internal Medicine
Background:
- Behçet's disease (BD) is a chronic, multisystem immune-mediated vasculitis.
- Inflammatory comorbid (IC) diseases can significantly impact BD's clinical course.
- Limited research exists on the prevalence and spectrum of IC diseases in BD patients.
Purpose of the Study:
- To determine the prevalence of inflammatory comorbid diseases in Behçet's disease.
- To characterize the clinical spectrum of these comorbidities in BD patients.
- To identify factors associated with the presence of IC disease in BD.
Main Methods:
- Retrospective analysis of 1591 BD patients from five tertiary centers.
- Systematic collection of demographic, clinical, and laboratory data.
- Evaluation of disease activity using the Behçet's Disease Current Activity Form (BDCAF).
Main Results:
- 15.3% of BD patients had identified inflammatory comorbidities.
- Most common comorbidities included axial spondyloarthritis (7.2%), familial Mediterranean fever (2.4%), and hidradenitis suppurativa (2.3%).
- Patients with IC disease showed increased anti-TNF treatment use; older age and longer disease duration were associated with IC disease.
Conclusions:
- Behçet's disease frequently co-occurs with other inflammatory conditions.
- The presence of IC disease may influence treatment decisions, including anti-TNF therapy.
- Clinicians should actively screen for and manage inflammatory comorbidities in BD patients.
Objectives:
Behçet's disease (BD) is a chronic, multisystem immune-mediated vasculitis. A significant number of patients with BD have inflammatory comorbid (IC) disease that can affect the clinical course of the disease. In the current literature, there is no study which investigated IC disease in BD. It was aimed to show the prevalence and clinical spectrum of IC disease in patients with BD.
Methods:
A total of 1591 patients diagnosed with BD and followed at five tertiary healthcare facilities were enrolled in the study. Patients were divided according to the presence of IC disease. Demographic characteristics, clinical manifestations, and laboratory parameters were systematically noted from medical records. The activity of the disease was evaluated by Behçet's Disease Current Activity Form (BDCAF).
Results:
Inflammatory comorbid diseases were identified in 246 (15.3%) patients. The most common comorbidities were axial spondyloarthritis (n = 115, 7.2%), familial Mediterranean fever (FMF) (n = 38, 2.4%), and hidradenitis suppurativa (n = 37, 2.3%). Patients with IC disease had a greater use of anti-TNF treatment (p = 0.03). In the multivariate analysis, older age, and longer disease duration were found to be significantly associated with IC disease in BD (p < 0.05).
Conclusion:
BD can be associated with other inflammatory conditions. Furthermore, patients with inflammatory comorbidities were more likely to receive anti-TNF therapy, although this may partly reflect treatment indications for the comorbid conditions themselves. Therefore, clinicians should remain vigilant for inflammatory comorbidities, as their recognition may have implications for therapeutic decision-making.
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