Ekelund Maria, Aalto Kristiina, Fasth Anders, Herlin Troels, Nielsen Susan, Nordal Ellen, Peltoniemi Suvi, Rygg Marite, Zak Marek, Berntson Lillemor
Department of Pediatrics, Ryhov County Hospital, Jönköping, Sweden.
Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Pediatr Rheumatol Online J. 2017 Feb 22;15(1):13. doi: 10.1186/s12969-017-0145-5.
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).
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.
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).
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.
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。
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。
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)。
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。