TY - JOUR
T1 - Disease activity at two consecutive registry visits and subsequent medication escalation for patients with juvenile idiopathic arthritis in the CARRA registry
AU - for the CARRA Registry Investigators
AU - Mannion, Melissa L.
AU - Aswani, Monica S.
AU - Hearld, K. Ria
AU - Smitherman, Emily A.
AU - Timmerman, Livie
AU - Curtis, Jeffrey R.
AU - Zic, C.
AU - Zhu, A.
AU - Zheng, Z.
AU - Zhao, Y. D.
AU - Zhang, Y. J.
AU - Zeft, A.
AU - Yomogida, K.
AU - Yeung, R.
AU - Yalcindag, A.
AU - Wu, E.
AU - Wright, T.
AU - Woolnough, L.
AU - Wooldridge, S.
AU - Wong, S.
AU - Williams, C.
AU - Widrick, K.
AU - Westheuser, V.
AU - Wershba, E.
AU - Weiss, P.
AU - Weiss, J.
AU - Waterfield, M.
AU - Walters, H.
AU - Wallgren, S.
AU - Walker, B.
AU - Wakefield, S.
AU - Wahezi, D.
AU - Wagner-Weiner, L.
AU - Vora, S.
AU - von Scheven, E.
AU - Verstegen, R.
AU - Verbsky, J.
AU - Vega-Fernandez, P.
AU - Vasquez, N.
AU - Varghese, C.
AU - Vandenbergen, S.
AU - Van Mater, H.
AU - Vallee, A.
AU - Valdovinos, R.
AU - Valcarcel, T.
AU - Twilt, M.
AU - Twachtman-Bassett, J.
AU - Tsin, C.
AU - Hays, K.
AU - Hahn, T.
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Objective: To account for the chronic time course of juvenile idiopathic arthritis (JIA), we assessed medication changes by disease activity patterns across 2 sequential timepoints. Methods: Patients with non-systemic JIA enrolled in the Childhood Arthritis and Rheumatology Research Alliance Registry with complete clinical Juvenile Arthritis Disease Activity Scores (cJADAS) at 6 and 12-month registry visits were included. Disease activity was classified by cJADAS categories (inactive/minimal, moderate/high). The primary outcome was disease modifying anti-rheumatic drug (DMARD) escalation at the 12-month visit. We examined the association between cJADAS patterns and DMARD escalation. Results: The cJADAS patterns across paired visits for 2,956 patients with JIA were: 71% persistent inactive/minimal, 25% persistent moderate/high, 2% “improving”, and 2% “flaring”. Only 10% of patients had DMARD escalation at the 12-month visit, including only 15% of patients with persistent moderate/high disease activity. In multivariable logistic regression adjusting for sociodemographic and clinical variables, DMARD escalation at the 12-month visit was associated with “flaring” disease activity (odds ratio [OR] 2.62, 95% confidence interval [CI] 1.33–5.18), DMARD escalation between the 6- and 12-month visits (OR 1.86, 95% CI 1.40–2.49) and morning stiffness (> 60 min 4.98, 95% CI 3.00–8.27), while age 15–19 years were less likely to escalate (OR 0.61, 95% CI 0.38–0.97). Conclusion: In a large multicenter registry of US patients with JIA, DMARD escalation at the 12-month visit was uncommon overall, even for those with persistent moderate/high disease activity. Our findings suggest that DMARD escalation in this cohort did not align well with a treat to target approach using cJADAS thresholds.
AB - Objective: To account for the chronic time course of juvenile idiopathic arthritis (JIA), we assessed medication changes by disease activity patterns across 2 sequential timepoints. Methods: Patients with non-systemic JIA enrolled in the Childhood Arthritis and Rheumatology Research Alliance Registry with complete clinical Juvenile Arthritis Disease Activity Scores (cJADAS) at 6 and 12-month registry visits were included. Disease activity was classified by cJADAS categories (inactive/minimal, moderate/high). The primary outcome was disease modifying anti-rheumatic drug (DMARD) escalation at the 12-month visit. We examined the association between cJADAS patterns and DMARD escalation. Results: The cJADAS patterns across paired visits for 2,956 patients with JIA were: 71% persistent inactive/minimal, 25% persistent moderate/high, 2% “improving”, and 2% “flaring”. Only 10% of patients had DMARD escalation at the 12-month visit, including only 15% of patients with persistent moderate/high disease activity. In multivariable logistic regression adjusting for sociodemographic and clinical variables, DMARD escalation at the 12-month visit was associated with “flaring” disease activity (odds ratio [OR] 2.62, 95% confidence interval [CI] 1.33–5.18), DMARD escalation between the 6- and 12-month visits (OR 1.86, 95% CI 1.40–2.49) and morning stiffness (> 60 min 4.98, 95% CI 3.00–8.27), while age 15–19 years were less likely to escalate (OR 0.61, 95% CI 0.38–0.97). Conclusion: In a large multicenter registry of US patients with JIA, DMARD escalation at the 12-month visit was uncommon overall, even for those with persistent moderate/high disease activity. Our findings suggest that DMARD escalation in this cohort did not align well with a treat to target approach using cJADAS thresholds.
UR - https://www.scopus.com/pages/publications/105012233236
UR - https://www.scopus.com/pages/publications/105012233236#tab=citedBy
U2 - 10.1186/s12969-025-01130-2
DO - 10.1186/s12969-025-01130-2
M3 - Article
C2 - 40696394
AN - SCOPUS:105012233236
SN - 1546-0096
VL - 23
JO - Pediatric Rheumatology
JF - Pediatric Rheumatology
IS - 1
M1 - 77
ER -