Tumor necrosis factor-α inhibitor-induced psoriasis in juvenile idiopathic arthritis patients.


Journal

Pediatric dermatology
ISSN: 1525-1470
Titre abrégé: Pediatr Dermatol
Pays: United States
ID NLM: 8406799

Informations de publication

Date de publication:
Sep 2019
Historique:
pubmed: 27 6 2019
medline: 29 2 2020
entrez: 27 6 2019
Statut: ppublish

Résumé

The development of psoriasis while on tumor necrosis factor inhibitors (TNFi) is a paradoxical effect of agents that treat psoriasis. There is a paucity of data available on this entity in juvenile idiopathic arthritis (JIA). Our objectives were to determine the prevalence of TNFi-induced psoriasis in patients with JIA at two pediatric centers, and psoriasis response to therapeutic modifications. We performed retrospective chart review on patients with JIA treated with TNFi (adalimumab, etanercept, infliximab) who developed psoriasis. TNFi-induced psoriasis was defined as an incident diagnosis of psoriasis after starting a TNFi. Patients with personal histories of psoriasis prior to TNFi therapy were excluded. Following diagnosis, responses to medication changes were defined based on physician assessments. Nine of 166 (5.4%) patients on TNFi for JIA were diagnosed with TNFi-induced psoriasis. All cases were female. One had a family history of psoriasis. The median age was 10 (range 2-16) years. Five (55%) patients experienced scalp psoriasis, including four (44%) with alopecia. Two (22%) patients achieved significant improvement after switching to different classes of biologic agents, while three (33%) patients had significant improvement following discontinuation of biologic therapy. One of five patients who switched to a different TNFi had complete resolution, while four had worsening symptoms or partial improvement. Our findings demonstrate the prevalence of TNFi-induced psoriasis in JIA at two centers. Though larger studies are needed, our data suggest discontinuation of TNFi or biologic class switching should be considered as treatment strategies in select patients.

Sections du résumé

BACKGROUND/OBJECTIVES OBJECTIVE
The development of psoriasis while on tumor necrosis factor inhibitors (TNFi) is a paradoxical effect of agents that treat psoriasis. There is a paucity of data available on this entity in juvenile idiopathic arthritis (JIA). Our objectives were to determine the prevalence of TNFi-induced psoriasis in patients with JIA at two pediatric centers, and psoriasis response to therapeutic modifications.
METHODS METHODS
We performed retrospective chart review on patients with JIA treated with TNFi (adalimumab, etanercept, infliximab) who developed psoriasis. TNFi-induced psoriasis was defined as an incident diagnosis of psoriasis after starting a TNFi. Patients with personal histories of psoriasis prior to TNFi therapy were excluded. Following diagnosis, responses to medication changes were defined based on physician assessments.
RESULTS RESULTS
Nine of 166 (5.4%) patients on TNFi for JIA were diagnosed with TNFi-induced psoriasis. All cases were female. One had a family history of psoriasis. The median age was 10 (range 2-16) years. Five (55%) patients experienced scalp psoriasis, including four (44%) with alopecia. Two (22%) patients achieved significant improvement after switching to different classes of biologic agents, while three (33%) patients had significant improvement following discontinuation of biologic therapy. One of five patients who switched to a different TNFi had complete resolution, while four had worsening symptoms or partial improvement.
CONCLUSIONS CONCLUSIONS
Our findings demonstrate the prevalence of TNFi-induced psoriasis in JIA at two centers. Though larger studies are needed, our data suggest discontinuation of TNFi or biologic class switching should be considered as treatment strategies in select patients.

Identifiants

pubmed: 31240749
doi: 10.1111/pde.13859
doi:

Substances chimiques

Antirheumatic Agents 0
Tumor Necrosis Factor-alpha 0
Infliximab B72HH48FLU
Adalimumab FYS6T7F842
Etanercept OP401G7OJC

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

613-617

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Daniel Groth (D)

Division of Pediatric Rheumatology, Goryeb Children's Hospital at Atlantic Health, Morristown, New Jersey.

Maria Perez (M)

Division of Pediatric Gastroenterology, Goryeb Children's Hospital at Atlantic Health, Morristown, New Jersey.

James R Treat (JR)

Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Leslie Castelo-Soccio (L)

Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Simona Nativ (S)

Division of Pediatric Rheumatology, Goryeb Children's Hospital at Atlantic Health, Morristown, New Jersey.

Pamela F Weiss (PF)

Division of Pediatric Rheumatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Sivia Lapidus (S)

Division of Pediatric Rheumatology, Hackensack University Medical Center, Hackensack Meridian Health, Hackensack, New Jersey.

Marissa J Perman (MJ)

Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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Classifications MeSH