Evidence map›Paper›PMID 42583531›Full record

ArticleRheumatology advances in practice2026

A stratified approach to juvenile idiopathic arthritis: leveraging machine learning to uncover subgroups of patients following treatment with etanercept.

Stephanie J W Shoop-Worrall, Saskia Lawson-Tovey, Lucy R Wedderburn, Kimme L Hyrich, Nophar Geifman, UK JIA Biologics Register Investigators, CAPS Investigators, CHARMS Investigators, CLUSTER Consortium

Abstract read
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Article in Rheumatology advances in practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Stephanie J W Shoop-WorrallCentre for Epidemiology Versus Arthritis, University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-9441-5535
Saskia Lawson-ToveyCentre for Genetics and Genomics Versus Arthritis, University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-8611-162X
Lucy R WedderburnCentre for Adolescent Rheumatology Versus Arthritis at UCL, UCLH and GOSH, London, UK.ORCID https://orcid.org/0000-0002-7495-1429
Kimme L HyrichCentre for Epidemiology Versus Arthritis, University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0001-8242-9262
Nophar GeifmanSchool of Health Sciences, Faculty of Health and Medical Sciences, University of Surrey, Surrey, UK.ORCID https://orcid.org/0000-0003-2956-6676
UK JIA Biologics Register Investigators, CAPS Investigators, CHARMS Investigators, CLUSTER Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To facilitate a stratified approach to treatment of JIA and uncover trajectory-based patterns of key clinical outcomes following etanercept (ETN) initiation in children and young people (CYP). Methods: ETN-naïve CYP with non-systemic JIA recruited to one of three UK prospective multicentre cohorts were selected if they started ETN between 2001 and 2019. JADAS71 (71-joint Juvenile Arthritis Disease Activity) components [active joint count, physician global assessment (PGA), parent global evaluation (PGE) and ESR] were collected in the year following ETN initiation. Clusters of CYP based on JADAS71 component trajectory patterns following ETN initiation were identified using multivariate group-based trajectory models, adjusting for year of ETN initiation. Multinomial logistic regression identified independent predictors of outcome clusters. In a subset of CYP with previously determined MTX trajectories, response clusters were compared descriptively. Results: In 1003 CYP, five clusters were identified following ETN initiation. In three clusters, JADAS components changed in parallel: fast improvers (16%), slow improvers (10%) and persistent disease (37%). In two, all components except for one improved over time: persistent PGA (7%) and persistent PGE (30%). Where both MTX and ETN trajectories were available ( Conclusion: Across multiple DMARDs, JIA disease activity does not always improve to similar degrees across the different features of disease. A majority of CYP initially experiencing persistent disease with MTX fall into a response group following ETN.

Indexed as

biologicsepidemiologyjuvenile idiopathic arthritisoutcomesstratified medicine

Identifiers

PMID42583531
PMCPMC13461192

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.