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Treatment to Target Using Recombinant Interleukin-1 Receptor Antagonist as First-Line Monotherapy in New-Onset Systemic Juvenile Idiopathic Arthritis: Results From a Five-Year Follow-Up Study.采用重组白细胞介素-1 受体拮抗剂作为一线单药治疗新诊断的全身型幼年特发性关节炎:一项为期 5 年随访研究的结果。
Arthritis Rheumatol. 2019 Jul;71(7):1163-1173. doi: 10.1002/art.40865. Epub 2019 May 25.
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Predictive factors and biomarkers for the 2-year outcome of uveitis in juvenile idiopathic arthritis: data from the Inception Cohort of Newly diagnosed patients with Juvenile Idiopathic Arthritis (ICON-JIA) study.幼年特发性关节炎葡萄膜炎 2 年结局的预测因素和生物标志物:幼年特发性关节炎(ICON-JIA)新诊断患者队列研究的数据。
Rheumatology (Oxford). 2019 Jun 1;58(6):975-986. doi: 10.1093/rheumatology/key406.
3
Treating juvenile idiopathic arthritis to target: recommendations of an international task force.靶向治疗幼年特发性关节炎:国际工作组的建议。
Ann Rheum Dis. 2018 Jun;77(6):819-828. doi: 10.1136/annrheumdis-2018-213030. Epub 2018 Apr 11.
4
Disease progression into adulthood and predictors of long-term active disease in juvenile idiopathic arthritis.幼年特发性关节炎向成年期的疾病进展及长期活动性疾病的预测因素。
Ann Rheum Dis. 2016 Jan;75(1):190-5. doi: 10.1136/annrheumdis-2014-206034. Epub 2014 Oct 31.
5
Early predictors of prognosis in juvenile idiopathic arthritis: a systematic literature review.幼年特发性关节炎预后的早期预测指标:系统文献回顾。
Ann Rheum Dis. 2015 Nov;74(11):1996-2005. doi: 10.1136/annrheumdis-2014-205265. Epub 2014 Jun 24.
6
The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-Out cohort.当代治疗方案管理下的儿童青少年特发性关节炎的结局:REACCh-Out 队列研究结果。
Ann Rheum Dis. 2015 Oct;74(10):1854-60. doi: 10.1136/annrheumdis-2014-205372. Epub 2014 May 19.
7
American College of Rheumatology provisional criteria for defining clinical inactive disease in select categories of juvenile idiopathic arthritis.美国风湿病学会选择的幼年特发性关节炎分类的临床无活动疾病定义的临时标准。
Arthritis Care Res (Hoboken). 2011 Jul;63(7):929-36. doi: 10.1002/acr.20497.
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Ongoing disease activity and changing categories in a long-term nordic cohort study of juvenile idiopathic arthritis.一项针对青少年特发性关节炎的长期北欧队列研究中的疾病活动持续情况及类别变化
Arthritis Rheum. 2011 Sep;63(9):2809-18. doi: 10.1002/art.30426.
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Radiographic and clinical outcome in early juvenile rheumatoid arthritis and juvenile spondyloarthropathy: a 3-year prospective study.幼年特发性关节炎和幼年脊柱关节炎早期的影像学及临床结局:一项为期3年的前瞻性研究
J Rheumatol. 2006 Jul;33(7):1382-91. Epub 2006 Jun 1.
10
Predictors of disease course and remission in systemic juvenile idiopathic arthritis: significance of early clinical and laboratory features.全身型幼年特发性关节炎疾病进程和缓解的预测因素:早期临床和实验室特征的意义
Arthritis Rheum. 2006 May;54(5):1595-601. doi: 10.1002/art.21774.

ReACCh-Out 队列中儿童青少年特发性关节炎的长期结局和疾病进程:一项双中心经验。

Long-term outcomes and disease course of children with juvenile idiopathic arthritis in the ReACCh-Out cohort: a two-centre experience.

机构信息

Department of Pediatrics, University of British Columbia.

British Columbia Children's Hospital, Vancouver, British Columbia.

出版信息

Rheumatology (Oxford). 2020 Dec 1;59(12):3727-3730. doi: 10.1093/rheumatology/keaa118.

DOI:10.1093/rheumatology/keaa118
PMID:32402087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7733713/
Abstract

OBJECTIVE

To assess long-term outcomes of children with JIA diagnosed in the biologic era.

METHODS

Chart review of patients prospectively enrolled in the Research in Arthritis in Canadian Children Emphasizing Outcomes inception cohort at two Canadian centres. Inactive disease and remission were defined according to Wallace criteria.

RESULTS

We included 247 of 254 (97%) eligible patients diagnosed 2005-10. At the last follow-up visit at a median age of 16.9 years, 47% were in remission off medications, 25% in remission on medications and 27% had active disease; 51% were on at least one anti-rheumatic medication (22% on biologics). Patients with systemic JIA had the highest frequency of remission off medications (70%) and patients with RF-positive polyarthritis had the lowest (18%) (P <0.05 by Fisher's exact test). Among 99 patients with oligoarthritis at enrolment, 14 (14%) had an oligoarthritis extended course. Forty-five patients (18%) had at least one erosion or joint space narrowing in X-rays or MRI, and two (0.8%) required joint replacement.

CONCLUSION

Relative to historical cohorts, this study suggests a reduction in JIA permanent damage, a more favourable prognosis for systemic JIA and a lower progression to oligoarthritis extended category. However, in an era of biologic therapy, one in four patients with JIA still enter adulthood with active disease and one in two still on treatment.

摘要

目的

评估生物制剂时代诊断的幼年特发性关节炎(JIA)患儿的长期结局。

方法

对在加拿大两个中心前瞻性入组的加拿大儿童关节炎研究中强调结局的研究队列中的患者进行图表回顾。根据 Wallace 标准定义疾病缓解和无活动。

结果

我们纳入了 2005-10 年诊断的 254 名符合条件患者中的 247 名。在中位数年龄为 16.9 岁的最后一次随访时,47%的患者停药后缓解,25%的患者在药物治疗下缓解,27%的患者疾病活动;51%的患者至少使用一种抗风湿药物(22%使用生物制剂)。全身型 JIA 患者停药后缓解率最高(70%),RF 阳性多关节炎患者缓解率最低(18%)(Fisher 确切检验,P<0.05)。在入组时患有少关节炎的 99 名患者中,14 名(14%)为少关节炎扩展型病程。45 名患者(18%)在 X 线或 MRI 上至少有一处侵蚀或关节间隙变窄,2 名(0.8%)需要关节置换。

结论

与历史队列相比,本研究表明 JIA 永久性损害减少,全身型 JIA 预后较好,少关节炎扩展型病程进展减少。然而,在生物治疗时代,仍有四分之一的 JIA 患者成年后仍有疾病活动,二分之一的患者仍在接受治疗。