Infliximab Paradoxical Psoriasis in a Cohort of Children With Inflammatory Bowel Disease.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 29 3 2019
medline: 15 9 2020
entrez: 29 3 2019
Statut: ppublish

Résumé

In adult inflammatory bowel disease (IBD) treated by anti-TNF antibodies, paradoxical psoriasis has an estimated prevalence of 1.6 to 22%, especially in infliximab (IFX)-treated patients. Little is known in the pediatric IBD (PIBD) populations. All patients ages from 2 to 18 years with Crohn disease (CD) or ulcerative colitis (UC) and treated for the first time by IFX between January 2002 and March 2014, were considered for inclusion in this retrospective study performed in a tertiary PIBD centre. Paradoxical psoriasis events together with clinical and biological data were collected in all patients. Comparisons between psoriasis and control groups were performed using univariate statistical analyses. One hundred and twenty-three CD patients and 24 UC patients were treated with IFX. Twenty patients (13.6%) experienced a paradoxical psoriasis. All of them were affected by CD. Perianal CD was more frequent in the psoriasis group (P = 0.033). Fourteen patients (70%) were in remission when skin lesions occurred. Paradoxical psoriasis was diagnosed 355 days (median, interquartile range [IQR] 239; 532) after the initiation of IFX corresponding to the eighth injection (median, IQR: 6; 15). Psoriasis lesions were controlled by local steroids in all cases and no patients discontinued IFX therapy. 13.6% of our IBD patients treated with IFX developed psoriasis during a median follow-up of 23.9 months (IQR: 11.6; 36.5). Crohn disease patients with perianal disease were at a higher risk to develop this common side effect.

Identifiants

pubmed: 30921262
doi: 10.1097/MPG.0000000000002349
doi:

Substances chimiques

Dermatologic Agents 0
Infliximab B72HH48FLU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-193

Auteurs

Olivier Courbette (O)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.

Camille Aupiais (C)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.
Université Paris Diderot, INSERM UMR 1123 (ECEVE).

Jerome Viala (J)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.

Jean-Pierre Hugot (JP)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.
Université Paris Diderot, INSERM UMR 1149.

Baptiste Louveau (B)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.

Lucienne Chatenoud (L)

Université Paris Descartes, Sorbonne Paris Cité.
INSERM U1151, CNRS UMR 8253, Hôpital Necker-Enfants Malades, Paris.

Emmanuelle Bourrat (E)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.
Assistance publique-Hôpitaux de Paris, Hôpital Saint Louis, France.

Christine Martinez-Vinson (C)

Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré.

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Classifications MeSH