Reversibility of alexithymia with effective treatment of moderate-to-severe psoriasis: longitudinal data from EPIDEPSO.


Journal

The British journal of dermatology
ISSN: 1365-2133
Titre abrégé: Br J Dermatol
Pays: England
ID NLM: 0004041

Informations de publication

Date de publication:
02 2019
Historique:
accepted: 26 09 2018
pubmed: 1 10 2018
medline: 15 2 2020
entrez: 1 10 2018
Statut: ppublish

Résumé

Alexithymia refers to difficulty in identifying and expressing emotions. Alexithymia is associated with high burden of disease in patients with psoriasis. To investigate whether alexithymia was reversible in patients with psoriasis following real-life therapeutic intervention. The Epidemiological Study in Patients with Recently Diagnosed Psoriasis (EPIDEPSO; NCT01964443) was a 1-year multicentre observational study investigating the prevalence of alexithymia and other psychosocial comorbidities in patients with psoriasis with ≤ 10 years' disease duration and eligible for systemic treatment. Alexithymia was assessed using the Toronto Alexithymia Scale (TAS-20) at baseline, 6 months and 1 year. There was a statistically significant decrease in the prevalence of alexithymia in the follow-up cohort, from 26·7% at baseline to 21·2% at 6 months and 18·8% at 1 year. More than half of the patients (n = 77, 53·8%) who were alexithymic at baseline experienced reversion of their alexithymia. Reversion of alexithymia was higher in patients who reached a high level of disease control, defined as ≥ 75% or ≥ 90% improvement in Psoriasis Area and Severity Index. Reversion of alexithymia was associated with dramatic improvement in quality of life, anxiety and depression. Moreover, hazardous alcohol use, highly prevalent in patients with alexithymia, was reduced almost threefold at 1 year. Alexithymia and associated high disease burden may be reversible in patients with effective treatment of psoriasis. Proactive recognition of patients who are unable to identify and express their feelings is important.

Sections du résumé

BACKGROUND
Alexithymia refers to difficulty in identifying and expressing emotions. Alexithymia is associated with high burden of disease in patients with psoriasis.
OBJECTIVES
To investigate whether alexithymia was reversible in patients with psoriasis following real-life therapeutic intervention.
METHODS
The Epidemiological Study in Patients with Recently Diagnosed Psoriasis (EPIDEPSO; NCT01964443) was a 1-year multicentre observational study investigating the prevalence of alexithymia and other psychosocial comorbidities in patients with psoriasis with ≤ 10 years' disease duration and eligible for systemic treatment. Alexithymia was assessed using the Toronto Alexithymia Scale (TAS-20) at baseline, 6 months and 1 year.
RESULTS
There was a statistically significant decrease in the prevalence of alexithymia in the follow-up cohort, from 26·7% at baseline to 21·2% at 6 months and 18·8% at 1 year. More than half of the patients (n = 77, 53·8%) who were alexithymic at baseline experienced reversion of their alexithymia. Reversion of alexithymia was higher in patients who reached a high level of disease control, defined as ≥ 75% or ≥ 90% improvement in Psoriasis Area and Severity Index. Reversion of alexithymia was associated with dramatic improvement in quality of life, anxiety and depression. Moreover, hazardous alcohol use, highly prevalent in patients with alexithymia, was reduced almost threefold at 1 year.
CONCLUSIONS
Alexithymia and associated high disease burden may be reversible in patients with effective treatment of psoriasis. Proactive recognition of patients who are unable to identify and express their feelings is important.

Identifiants

pubmed: 30269346
doi: 10.1111/bjd.17259
doi:

Substances chimiques

Dermatologic Agents 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

397-403

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2018 British Association of Dermatologists.

Auteurs

F Sampogna (F)

Clinical Epidemiology Unit, Dermatological Hospital IDI-IRCCS FLMM, Rome, Italy.

L Puig (L)

Universitat Autònoma de Barcelona, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

P Spuls (P)

Department of Dermatology, University of Amsterdam, Amsterdam, the Netherlands.

G Girolomoni (G)

University of Verona, Verona, Italy.

M A Radtke (MA)

Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

B Kirby (B)

St Vincent's University Hospital, Dublin, Ireland.

M Brunori (M)

Janssen-Cilag, Paris, France.

P Bergmans (P)

Janssen-Cilag BV, Breda, the Netherlands.

P Smirnov (P)

Janssen Pharmaceutica NV, Moscow, Russia.

J Rundle (J)

Janssen-Cilag Ltd, High Wycombe, U.K.

A Castiglia (A)

Janssen Cilag SpA, Cologno Monzese, Italy.

F Lavie (F)

Janssen-Cilag, Paris, France.

C Paul (C)

Toulouse University and CHU Hôpital Larrey, Toulouse, France.

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