Treatment response to systemic therapies in pediatric-onset versus adult-onset psoriasis
a longitudinal real-world study.
Li S, Jiang Y, Muheyati D, Zhang Y, Dai M, Yu Q, Huang D, Wang Y, Yu Q, Shi Y
Journal of Dermatological TreatmentIn the feed 23 Sep 2026, published online 23 Sep 2026, issue 2026 Dec, added to PubMed 23 Sep 2026
Topics: PsoriasisPhotodermatology & sun protectionPediatric dermatology
Abstract
BACKGROUNDPsoriasis may present with onset in childhood or adulthood, reflecting distinct clinical patterns. Whether treatment response differs between these groups remains unclear, particularly across systemic therapies in real-world settings.
OBJECTIVESTo compare longitudinal treatment responses between patients with pediatric-onset psoriasis (POPPs) and patients with adult-onset psoriasis (AOPPs) across systemic therapies in real-world practice.
METHODSPsoriasis patients receiving interleukin (IL)-17 inhibitors, IL-23 or IL-12/23 inhibitors, methotrexate, or phototherapy were included. Primary outcomes were Psoriasis Area and Severity Index (PASI) 90 and Dermatology Life Quality Index (DLQI) 0/1 at 1, 2, 3, and 6 months. Associations between onset group and treatment outcomes were assessed using generalized estimating equation (GEE) models with adjustment for potential confounders.
RESULTSAmong 1873 patients, 576 received IL-17 inhibitors, POPPs had higher PASI90 rates at 1-6 months (26.1%-62.2% vs. 14.6%-51.2%) and higher DLQI 0/1 response rates (30.6%-45.0% vs. 20.3%-40.0%) than AOPPs. Multivariable GEE analyses further demonstrated that, compared with POPPs, AOPPs had lower odds of achieving PASI90 (adjusted odds ratios 0.62, 95% confidence interval 0.42-0.89; p = .011). No significant differences were shown among patients treated with IL-23 or IL-12/23 inhibitors, methotrexate, or phototherapy.
CONCLUSIONSPediatric-onset psoriasis was associated with improved clinical outcomes during IL-17 inhibitor therapy. Further comparative-effectiveness studies are warranted to determine whether onset pattern may contribute to individualized treatment selection.
Abstract from PubMed
PMID 42775584 · DOI 10.1080/09546634.2026.2734961