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本文引用的文献

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New therapies for psoriasis and psoriatic arthritis.银屑病和银屑病关节炎的新疗法。
Curr Opin Rheumatol. 2016 May;28(3):204-10. doi: 10.1097/BOR.0000000000000274.
2
A Family History of Psoriasis in a First-degree Relative in Children with JIA: to Include or Exclude?幼年特发性关节炎患儿一级亲属的银屑病家族史:纳入还是排除?
J Rheumatol. 2016 May;43(5):944-7. doi: 10.3899/jrheum.150555. Epub 2016 Mar 15.
3
The conundrum of juvenile psoriatic arthritis.青少年银屑病关节炎的难题。
Clin Exp Rheumatol. 2015 Sep-Oct;33(5 Suppl 93):S40-3. Epub 2015 Oct 15.
4
The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing.白细胞介素-23-白细胞介素-17免疫轴:从机制到治疗测试
Nat Rev Immunol. 2014 Sep;14(9):585-600. doi: 10.1038/nri3707.
5
Juvenile Psoriatic Arthritis (JPsA): juvenile arthritis with psoriasis?幼年特发性关节炎(JPsA):伴银屑病的幼年关节炎?
Pediatr Rheumatol Online J. 2013 Mar 15;11(1):11. doi: 10.1186/1546-0096-11-11.
6
Psoriatic juvenile idiopathic arthritis: a tale of two subgroups.银屑病性幼年特发性关节炎:两个亚组的故事。
Curr Opin Rheumatol. 2011 Sep;23(5):437-43. doi: 10.1097/BOR.0b013e328348b278.
7
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.
8
Clinical comparison of early-onset psoriatic and non-psoriatic oligoarticular juvenile idiopathic arthritis.早发型银屑病与非银屑病寡关节型幼年特发性关节炎的临床对比。
Clin Exp Rheumatol. 2011 May-Jun;29(3):582-8. Epub 2011 Jun 30.
9
Spondyloarthritis in a pediatric population: risk factors for sacroiliitis.儿童人群中的脊柱关节炎:与骶髂关节炎相关的风险因素。
J Rheumatol. 2010 Nov;37(11):2402-8. doi: 10.3899/jrheum.100014. Epub 2010 Aug 3.
10
Comparison of Vancouver and International League of Associations for rheumatology classification criteria for juvenile psoriatic arthritis.青少年银屑病关节炎的温哥华分类标准与国际风湿病协会联盟分类标准的比较。
Arthritis Rheum. 2008 Jan 15;59(1):51-8. doi: 10.1002/art.23240.

青少年特发性关节炎分类及预后中的银屑病及相关变量——一项八年随访研究

Psoriasis and associated variables in classification and outcome of juvenile idiopathic arthritis - an eight-year follow-up study.

作者信息

Ekelund Maria, Aalto Kristiina, Fasth Anders, Herlin Troels, Nielsen Susan, Nordal Ellen, Peltoniemi Suvi, Rygg Marite, Zak Marek, Berntson Lillemor

机构信息

Department of Pediatrics, Ryhov County Hospital, Jönköping, Sweden.

Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.

出版信息

Pediatr Rheumatol Online J. 2017 Feb 22;15(1):13. doi: 10.1186/s12969-017-0145-5.

DOI:10.1186/s12969-017-0145-5
PMID:28222745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5320636/
Abstract

BACKGROUND

To study the impact of psoriasis and features associated with psoriasis on classification and outcome in a population-based follow-up cohort of children with juvenile idiopathic arthritis (JIA).

METHODS

In all, 440 children with JIA were followed for a median of 8 years in a prospective Nordic population-based cohort study. Data for remission was available for 427 of these children. The presence of psoriasis, psoriasis-like rash, dactylitis, nail pitting, enthesitis, tenosynovitis and heredity was assessed in relation to ILAR classification and remission.

RESULTS

Clinical findings associated with psoriasis developed consecutively during the 8-year period. Six of 14 children with psoriasis were not classified as juvenile psoriatic arthritis according to the ILAR criteria at 8 year follow-up. Dactylitis was more common in children with early onset of JIA. After 8 years we found a cumulative median number of eleven arthritic joints in children with psoriasis or psoriasis-like rash compared with six in the rest of the cohort (p = 0.02). Also, the chance for not being in remission after 8 years increased significantly in patients with psoriasis, psoriasis-like rash or at least two of: 1) first-degree heredity for psoriasis or psoriatic arthritis, 2) dactylitis or 3) nail pitting, compared with the rest of the group (OR 3.32, p = 0.010).

CONCLUSIONS

Our results indicate a more severe disease over time in psoriasis-associated JIA, as features of psoriasis develop during the disease course. This group is a major challenge to encompass in a future JIA classification in order to facilitate early tailored treatment.

摘要

背景

在一项基于人群的青少年特发性关节炎(JIA)儿童随访队列研究中,探讨银屑病及银屑病相关特征对分类和预后的影响。

方法

在一项前瞻性的基于北欧人群的队列研究中,对440例JIA儿童进行了为期8年的随访。其中427例儿童有缓解数据。评估银屑病、银屑病样皮疹、指(趾)炎、甲凹点、附着点炎、腱鞘炎和遗传因素与国际风湿病联盟(ILAR)分类及缓解情况的关系。

结果

在8年期间,与银屑病相关的临床特征相继出现。在8年随访时,14例银屑病患儿中有6例未根据ILAR标准被分类为青少年银屑病关节炎。指(趾)炎在JIA起病较早的儿童中更为常见。8年后,我们发现银屑病或银屑病样皮疹患儿的关节炎关节累积中位数为11个,而队列中其他患儿为6个(p = 0.02)。此外,与其他组相比,患有银屑病、银屑病样皮疹或至少具备以下两项的患者在8年后未缓解的几率显著增加:1)银屑病或银屑病关节炎的一级遗传、2)指(趾)炎或3)甲凹点(比值比3.32,p = 0.010)。

结论

我们的结果表明,随着疾病进展,银屑病相关的JIA病情会更严重,因为银屑病特征在病程中逐渐出现。为了便于早期进行针对性治疗,这一群体在未来的JIA分类中是一个重大挑战。