Pediatric rheumatology

Trajectories of disease activity in patients with JIA in the Childhood Arthritis and Rheumatology Research Alliance Registry

Rheumatology (Oxford)Published Registry cohort study

Authors' conclusion

Five trajectories of JIA disease activity, and associated baseline variables, were identified.

Study context

Population
JIA patients in the CARRA Registry enrolled within 3 months of diagnosis (15 June 2015 to 6 December 2017) with at least two cJADAS10 scores and 24 months of follow-up
Participants
746 patients
Exposure
High, Rapidly Decreasing (HRD) vs High, Slowly Decreasing (HSD) vs High, Increasing (HI) vs Moderate, Persistent (MP) vs MD
  • HRDn = 199reference
  • HSDn = 154
  • HIn = 39
  • MPn = 218
  • MDn = 136
Outcome
Trajectories of cJADAS10 and associated baseline characteristics
Follow-up
2 years
Methodological detailslatent growth curve models, 2-year trajectories
  • Latent growth curve models
  • 2-year trajectories

Main finding

As reported in the abstract

cJADAS10 trajectory groups

Observational data: associations, not effects.

Further findings

Baseline characteristics associated with trajectories

HSD vs HRD: more likely older, lower PGA, normal inflammatory markers, longer time to first biologic, and taken systemic steroids
HI vs HRD: more likely ANA negative, longer time to first biologic, less likely taking a csDMARD
MP vs MD: more likely older, lower household income, longer time to diagnosis, markers of higher disease activity

Original publication

Trajectories of disease activity in patients with JIA in the Childhood Arthritis and Rheumatology Research Alliance Registry. Rheumatology (Oxford). Published 15 June 2022. doi:10.1093/rheumatology/keac335

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.