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在CARRA注册研究中,青少年特发性关节炎患者连续两次注册访视时的疾病活动情况及随后的药物升级情况。

Disease activity at two consecutive registry visits and subsequent medication escalation for patients with juvenile idiopathic arthritis in the CARRA registry.

作者信息

Mannion Melissa L, Aswani Monica S, Hearld K Ria, Smitherman Emily A, Timmerman Livie, Curtis Jeffrey R

机构信息

University of Alabama at Birmingham, 1600 7th Ave S, CPPN G10, Birmingham, AL 35233, USA.

出版信息

Pediatr Rheumatol Online J. 2025 Jul 22;23(1):77. doi: 10.1186/s12969-025-01130-2.

Abstract

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.

摘要

目的

为解释青少年特发性关节炎(JIA)的慢性病程,我们通过两个连续时间点的疾病活动模式评估了药物变化。

方法

纳入在儿童关节炎和风湿病研究联盟注册中心登记的非系统性JIA患者,这些患者在登记访视的6个月和12个月时具有完整的青少年关节炎疾病活动评分(cJADAS)。疾病活动根据cJADAS类别(无活动/最低、中度/高度)进行分类。主要结局是在12个月访视时改善病情抗风湿药物(DMARD)的升级。我们研究了cJADAS模式与DMARD升级之间的关联。

结果

2956例JIA患者配对访视的cJADAS模式为:71%持续无活动/最低,25%持续中度/高度,2%“改善”,2%“复发”。仅10%的患者在12个月访视时有DMARD升级,其中仅15%的患者有持续中度/高度疾病活动。在对社会人口统计学和临床变量进行调整的多变量逻辑回归分析中,12个月访视时的DMARD升级与“复发”疾病活动相关(比值比[OR]2.62,95%置信区间[CI]1.33 - 5.18)、6至12个月访视期间的DMARD升级(OR 1.86,95% CI 1.40 - 2.49)以及晨僵(>60分钟 4.98,95% CI 3.00 - 8.27)相关,而15至19岁的患者升级可能性较小(OR 0.61,95% CI 0.38 - 0.97)。

结论

在美国一个大型多中心JIA患者注册中心,总体而言,12个月访视时DMARD升级并不常见,即使对于那些有持续中度/高度疾病活动的患者也是如此。我们的研究结果表明,该队列中的DMARD升级与使用cJADAS阈值的达标治疗方法不太一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1e1/12285171/10ad31707a94/12969_2025_1130_Fig1_HTML.jpg

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