Clinical features and a Nomogram for predicting clinical response in juvenile dermatomyositis associated interstitial lung disease
- Journal
- The Journal of rheumatology (Q1)
- Published
- 15 September 2026
- Study design
- Retrospective cohort
- Evidence level
- Level 4, Very Low (CEBM 4)
- Authors
- Xinwei Shi, Junmei Zhang, Shipeng Li, Xiaohua Tan, Li Li, Jianghong Deng, et al.
- PMID
- 42744404
- DOI
- 10.3899/jrheum.2026-0380
Why clinicians should know about it
- Picked for Rheumatology (paper of the day, 18 September 2026): Nomogram predicts response in juvenile dermatomyositis ILD
Abstract
OBJECTIVE: Juvenile dermatomyositis (JDM) is a rare autoimmune disease and accompany by interstitial lung disease (ILD), a major cause of morbidity and mortality. However, data on clinical features and prognosis of JDM-ILD in Chinese pediatric populations remain limited. The aim is to characterize the clinical features, treatment options and prognosis of JDM-ILD in Chinese pediatric patients, and to develop a nomogram for predicting clinical response. METHODS: We retrospectively enrolled 244 JDM-ILD patients from Beijing Children's Hospital (May 2015-January 2026). Demographic, clinical, laboratory, treatment, and prognostic data were collected. Clinical response was assessed through a combination of PRINTO-defined clinical inactive disease (CID) , respiratory symptoms and HRCT. Independent prognostic factors were identified using Cox regression analysis and incorporated into a nomogram. Model performance was assessed using C-index, calibration curves and decision curve analysis (DCA). RESULTS: Among 244 patients (55.7% female, median onset age 5.7 years), anti-MDA5 (32.0%) and anti-NXP2 (13.9%) were the most prevalent autoantibodies. At last follow-up visit, 202 patients (82.8%) achieved CID, with CID rates increasing progressively over time. A total of three patients who tested positive for anti-MDA5 antibody died of RP-ILD (median survival 2.7 months). Multivariable Cox regression identified combination therapy with JAK inhibitors (HR 2.09, 95%CI 1.25-3.50) or IL-6 inhibitors (HR 1.83, 95%CI 1.07-3.12) and Gottron's sign (HR 1.80, 95%CI 1.10-2.96) as favorable factors for CID, while high-risk status (HR 0.23, 95%CI 0.10-0.57), higher DAS skin score (HR 0.71, 95%CI 0.48-1.00), and higher neutrophil-to-lymphocyte ratio (NLR) (HR 0.84, 95%CI 0.72-0.97) predicted lower probability of CID. The nomogram showed predictive performance in both training cohort (AUC: 0.67, 0.77, and 0.78 at 1, 3, and 5 years) and testing cohort (AUC: 0.60, 0.78 and 0.77 at 1, 3, and 5 years). CONCLUSION: This nomogram for predicting clinical response in Chinese pediatric JDM-ILD patients integrates clinical features and treatment variables to enable individualized risk stratification. Combination therapy with JAK or IL-6 inhibitors demonstrates promising efficacy and may improve outcomes.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.