Vasculitis & polymyalgia rheumatica

The impact of demographics on organ damage in Behçet’s syndrome: a cross-sectional analysis of the international PROBE cohort

Rheumatology (Oxford)Published Cross-sectional study

An erratum to this article was published (Rheumatology (Oxford), 5 Mar 2026 ↗)

Authors' conclusion

This study demonstrates how the extent, prevalence and characteristics of damage in BS vary with demographic factors, underscoring their importance in research and personalized management.

Study context

Population
Patients with Behçet's syndrome, international multiethnic PROBE cohort
Participants
970 patients
Exposure
Demographic factors and organ damage
Outcome
Extent and prevalence of organ damage measured by the Behçet's syndrome (BS) Overall Damage Index (BODI)
Methodological detailsancillary analysis of the PROBE project, multiethnic cohort, multivariate linear and logistic regression
  • Ancillary analysis of the PROBE project
  • Multiethnic cohort
  • Multivariate linear and logistic regression

Main finding

As reported in the abstract

Damage (BODI) by demographics
Median BS Overall Damage Index (BODI) score (IQR)
1 (0-3)
Patients with BODI ≥1
65.6%
Males: higher damage, β
0.103
Males: total damage prevalence, adjOR (per 10 years)
1.7
Males: ocular damage, adjOR
1.6
Males: vascular damage, adjOR
2.1
Age: greater damage, β
0.104
Age: overall damage, adjOR
1.4
Age: neuropsychiatric damage, adjOR
1.2
Age: miscellaneous damage, adjOR
2.0
Low education: overall damage, adjOR
1.9
Low education: ocular damage, adjOR
1.6
North African vs South European: greater damage, β
0.400
North African vs Middle Eastern: greater damage, β
0.314
North African vs South European: overall damage, adjOR
13.9
North African vs Middle Eastern: overall damage, adjOR
10.7

Observational data: associations, not effects.

Original publication

The impact of demographics on organ damage in Behçet’s syndrome: a cross-sectional analysis of the international PROBE cohort. Rheumatology (Oxford). Published 29 November 2025. doi:10.1093/rheumatology/keaf636

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