Prevalence of ultrasound and clinical findings suggestive of inflammatory arthritis in children with skin psoriasis

Author:

Coronel Luis12ORCID,Gouze Hélène13ORCID,Gudu Tania1,Ruel-Gagné Sophie1,Padovano Ilaria1,Costantino Félicie14,Vidal François1,Breban Maxime14ORCID,Mahé Emmanuel5,D’Agostino Maria-Antonietta146ORCID

Affiliation:

1. Rheumatology Division, Hôpital Ambroise-Paré, APHP-Université Paris-Saclay , France

2. Rheumatology Division, Hospital Universitari Vall d’Hebron , Barcelona, Spain

3. Inserm U1018, Center for Research in Epidemiology and Population Health “Integrative Respiratory Epidemiology” Team, Paris-Saclay University , Villejuif, France

4. Infection and Inflammation, UMR 1173, Inserm, UVSQ/Paris-Saclay University, Laboratory of Excellence INFLAMEX , Montigny-le-Bretonneux, France

5. Dermatology Department, Centre Hospitalier Victor Dupouy , Argenteuil, France

6. Rheumatology Department, Catholic University of Sacred Heart, Fondazione Policlinico Universitario Agostino Gemelli IRCSS , Rome, Italy

Abstract

Abstract Objective To evaluate the prevalence of clinical and US (grey-scale and Doppler) abnormalities in joints, periarticular structures and nails of children affected by skin psoriasis (PsO). Methods We conducted a cross-sectional study including consecutive children affected by PsO. A systematic clinical and US evaluation of joints, entheses, tendons and nails were performed by independent examiners blinded to each other’s assessment. Results A total of 57 children [26 girls (46%)] with a mean age of 9 years (s.d. 4) were divided into two groups, asymptomatic (Asy, 42 children) and symptomatic (Sy, 15 children), according to musculoskeletal pain. Differences were observed between the two groups in relation to age [9 years (s.d. 3) vs 11 years (s.d. 4), P < 0.05], PsO duration [2.4 years (s.d. 2.4) vs 5.4 years (s.d. 3.9), P < 0.001], systemic treatment [23 (54.8%) vs 2 [13.3%], P < 0.01], tender joint count [0 vs 12 children (80%), P < 0.001], swollen joint count [0 vs 3 children (20%), P < 0.01] and entheseal pain [0 vs 10 (66.7%), P < 0.001] in Asy and Sy children, respectively. US evaluation showed statistically significant differences between the Asy and Sy groups for the presence of US abnormalities [16/42 (38%) vs 12/15 (80%)], synovitis [1/42 (2%) vs 4/15 (25%)] and enthesitis [4/42 (9.5%) vs 5/15 (33%)]. Three children in the Sy group were classified with juvenile PsA (JPsA). Conclusions US abnormalities were higher in the Sy group, with synovitis and enthesitis as the most prevalent findings. Asy patients were more frequently under systemic treatment. US and a systematic clinical evaluation are useful tools for detecting subclinical JPsA in children with PsO and musculoskeletal symptoms.

Funder

Celgene-AMGEN

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference25 articles.

1. A systematic review of worldwide epidemiology of psoriasis;Michalek;J Eur Acad Dermatol Venereol,2017

2. International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001;Petty;J Rheumatol,2004

3. Reduced joint assessment vs comprehensive assessment for ultrasound detection of synovitis in juvenile idiopathic arthritis;Collado;Rheumatology (Oxford),2013

4. Reliability of ultrasonography to detect inflammatory lesions and structural damage in juvenile idiopathic arthritis;Ventura-Ríos;Pediatr Rheumatol,2018

5. Current state of musculoskeletal ultrasound in paediatric rheumatology: results of an international survey;Magni-Manzoni;Rheumatology (Oxford),2014

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