TY - JOUR
T1 - Towards stratified treatment of JIA
T2 - machine learning identifies subtypes in response to methotrexate from four UK cohorts
AU - CLUSTER consortium
AU - Shoop-Worrall, Stephanie J.W.
AU - Lawson-Tovey, Saskia
AU - Wedderburn, Lucy R.
AU - Hyrich, Kimme L.
AU - Geifman, Nophar
AU - Kimonyo, Aline
AU - McNeece, Alyssia
AU - Dick, Andrew
AU - Morris, Andrew
AU - Yarwood, Annie
AU - Ramanan, Athimalaipet
AU - Jebson, Bethany R.
AU - Wallace, Chris
AU - Dastros-Pitei, Daniela
AU - Tarasek, Damian
AU - Ralph, Elizabeth
AU - Carlsson, Emil
AU - Robinson, Emily
AU - Sumner, Emma
AU - Merali, Fatema
AU - Dekaj, Fatjon
AU - Neale, Helen
AU - Al-Mossawi, Hussein
AU - Roberts, Jacqui
AU - Gritzfeld, Jenna F.
AU - Fairlie, Joanna
AU - Bowes, John
AU - Ioannou, John
AU - Kartawinata, Melissa
AU - Tordoff, Melissa
AU - Barnes, Michael
AU - Beresford, Michael W.
AU - Stadler, Michael
AU - Martin, Paul
AU - Kallala, Rami
AU - Ng, Sandra
AU - Smith, Samantha
AU - Clarke, Sarah
AU - Raychaudhuri, Soumya
AU - Eyre, Stephen
AU - Mukherjee, Sumanta
AU - Duerr, Teresa
AU - Sornasse, Thierry
AU - Alexiou, Vasiliki
AU - Burton, Victoria J.
AU - Lin, Wei Yu
AU - Thomson, Wendy
AU - Wanstall, Zoe
N1 - Publisher Copyright:
© 2023
PY - 2024/2/1
Y1 - 2024/2/1
N2 - Background: Methotrexate (MTX) is the gold-standard first-line disease-modifying anti-rheumatic drug for juvenile idiopathic arthritis (JIA), despite only being either effective or tolerated in half of children and young people (CYP). To facilitate stratified treatment of early JIA, novel methods in machine learning were used to i) identify clusters with distinct disease patterns following MTX initiation; ii) predict cluster membership; and iii) compare clusters to existing treatment response measures. Methods: Discovery and verification cohorts included CYP who first initiated MTX before January 2018 in one of four UK multicentre prospective cohorts of JIA within the CLUSTER consortium. JADAS components (active joint count, physician (PGA) and parental (PGE) global assessments, ESR) were recorded at MTX start and over the following year. Clusters of MTX ‘response’ were uncovered using multivariate group-based trajectory modelling separately in discovery and verification cohorts. Clusters were compared descriptively to ACR Pedi 30/90 scores, and multivariate logistic regression models predicted cluster-group assignment. Findings: The discovery cohorts included 657 CYP and verification cohorts 1241 CYP. Six clusters were identified: Fast improvers (11%), Slow Improvers (16%), Improve-Relapse (7%), Persistent Disease (44%), Persistent PGA (8%) and Persistent PGE (13%), the latter two characterised by improvement in all features except one. Factors associated with clusters included ethnicity, ILAR category, age, PGE, and ESR scores at MTX start, with predictive model area under the curve values of 0.65–0.71. Singular ACR Pedi 30/90 scores at 6 and 12 months could not capture speeds of improvement, relapsing courses or diverging disease patterns. Interpretation: Six distinct patterns following initiation of MTX have been identified using methods in artificial intelligence. These clusters demonstrate the limitations in traditional yes/no treatment response assessment (e.g., ACRPedi30) and can form the basis of a stratified medicine programme in early JIA. Funding: Medical Research Council, Versus Arthritis, Great Ormond Street Hospital Children's Charity, Olivia's Vision, and the National Institute for Health Research.
AB - Background: Methotrexate (MTX) is the gold-standard first-line disease-modifying anti-rheumatic drug for juvenile idiopathic arthritis (JIA), despite only being either effective or tolerated in half of children and young people (CYP). To facilitate stratified treatment of early JIA, novel methods in machine learning were used to i) identify clusters with distinct disease patterns following MTX initiation; ii) predict cluster membership; and iii) compare clusters to existing treatment response measures. Methods: Discovery and verification cohorts included CYP who first initiated MTX before January 2018 in one of four UK multicentre prospective cohorts of JIA within the CLUSTER consortium. JADAS components (active joint count, physician (PGA) and parental (PGE) global assessments, ESR) were recorded at MTX start and over the following year. Clusters of MTX ‘response’ were uncovered using multivariate group-based trajectory modelling separately in discovery and verification cohorts. Clusters were compared descriptively to ACR Pedi 30/90 scores, and multivariate logistic regression models predicted cluster-group assignment. Findings: The discovery cohorts included 657 CYP and verification cohorts 1241 CYP. Six clusters were identified: Fast improvers (11%), Slow Improvers (16%), Improve-Relapse (7%), Persistent Disease (44%), Persistent PGA (8%) and Persistent PGE (13%), the latter two characterised by improvement in all features except one. Factors associated with clusters included ethnicity, ILAR category, age, PGE, and ESR scores at MTX start, with predictive model area under the curve values of 0.65–0.71. Singular ACR Pedi 30/90 scores at 6 and 12 months could not capture speeds of improvement, relapsing courses or diverging disease patterns. Interpretation: Six distinct patterns following initiation of MTX have been identified using methods in artificial intelligence. These clusters demonstrate the limitations in traditional yes/no treatment response assessment (e.g., ACRPedi30) and can form the basis of a stratified medicine programme in early JIA. Funding: Medical Research Council, Versus Arthritis, Great Ormond Street Hospital Children's Charity, Olivia's Vision, and the National Institute for Health Research.
KW - Epidemiology
KW - Juvenile idiopathic arthritis
KW - Machine learning
KW - Methotrexate
KW - Treatment outcome
UR - http://www.scopus.com/inward/record.url?scp=85181901214&partnerID=8YFLogxK
U2 - 10.1016/j.ebiom.2023.104946
DO - 10.1016/j.ebiom.2023.104946
M3 - Article
C2 - 38194741
AN - SCOPUS:85181901214
SN - 2352-3964
VL - 100
JO - eBioMedicine
JF - eBioMedicine
M1 - 104946
ER -