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.
Abstract

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