Spondyloarthritis & psoriatic arthritis

Incidence, baseline-associated factors and burden of difficult-to-manage axial spondyloarthritis: a 10-year analysis of the DESIR cohort

RMD OpenPublished Prospective cohort study

Authors' conclusion

In this recent-onset axSpA inception cohort with long-term follow-up, D2M-axSpA was rare, rarely associated with true treatment refractoriness or structural progression and was accompanied by a persistent disease burden carrying a substantial socio-economic impact

Study context

Population
Patients from the French prospective DESIR cohort fulfilling ASAS 2009 criteria for axSpA and exposed to ≥1 biologic disease-modifying antirheumatic drug (bDMARD)exposed to ≥1 bDMARD
Participants
177 patients
Exposure
Difficult-to-manage axial spondyloarthritis (D2M-axSpA) vs no D2M-axSpA for long-term outcomes
Outcome
Cumulative incidence of D2M-axSpA and TR-axSpA
Follow-up
Up to 10 years
Methodological detailsinception cohort, recent-onset axSpA, up to 10 years of follow-up, Cox proportional hazards models
  • Inception cohort
  • Recent-onset axSpA
  • Up to 10 years of follow-up
  • Cox proportional hazards models

Main finding

As reported in the abstract

Cumulative incidence of D2M-axSpA

D2M-axSpA, ASAS definition

6.8%

95% CI 2.4 to 11.0

D2M-axSpA, extended definition

14.4%

95% CI 8.3 to 20.2

TR-axSpA, ASAS definition

0.7%

TR-axSpA, extended definition

3.7%

Observational data: associations, not effects.

Further findings

Fibromyalgia prevalence during follow-up (extended definition)

Opioid use (extended definition)

OutcomeD2M-axSpANo D2M-axSpA
Cumulative number of medical visits (extended definition)11060

Baseline factors associated with D2M-axSpA (extended definition)

Female sex and higher baseline disease activity associated with development of D2M-axSpA

Original publication

Incidence, baseline-associated factors and burden of difficult-to-manage axial spondyloarthritis: a 10-year analysis of the DESIR cohort. RMD Open. Published 7 September 2026. doi:10.1136/rmdopen-2026-007094

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