Correlation of serum level of squamous cell carcinoma antigen with severity of cutaneous psoriasis, assessed using the simplified psoriasis index.

Biomarker Psoriasis Psoriasis Assessment Severity Index (PASI) Squamous cell carcinoma antigen (SCCA)

Journal

Annales de dermatologie et de venereologie
ISSN: 0151-9638
Titre abrégé: Ann Dermatol Venereol
Pays: France
ID NLM: 7702013

Informations de publication

Date de publication:
28 Feb 2024
Historique:
received: 16 09 2022
revised: 25 07 2023
accepted: 27 09 2023
medline: 1 3 2024
pubmed: 1 3 2024
entrez: 29 2 2024
Statut: aheadofprint

Résumé

Squamous cell carcinoma antigen (SCCA) is a biomarker of disease progression in squamous cell carcinoma but also contributes to the pathogenesis of psoriasis. Eight previous studies have shown a correlation between psoriasis severity, assessed using the Psoriasis Assessment Severity Index or body surface area, and serum level of SCCA, mainly SCCA2, assessed by means of non-commercial tests. We examined the correlation between serum SCCA level, measured with a commercial kit, and psoriasis severity assessed using the Simplified Psoriasis Index (SPI). We conducted a prospective, non-interventional, single-centre study at the University Hospital of Tours over 18 months. The primary endpoint was same-day measurement of serum SCCA level and the psoriasis severity score on the professional version of the SPI (proSPI-s) at both baseline and follow-up. Secondary endpoints were same-day measurement of serum SCCA level and the proSPI psychosocial score (proSPI-p), proSPI treatment score, Dermatology Life Quality Index (DLQI), and inflammation parameters (C-reactive protein level, neutrophil-to-lymphocyte ratio). We included 50 psoriasis patients. Serum SCCA level was correlated with the proSPI-s at baseline and follow-up (Spearman r = 0.686 and r = 0.674, p < 0.0001) for both. It was correlated with the proSPI-p and DLQI. Serum SCCA level was not correlated with either neutrophil-to-lymphocyte ratio (r = 0.083) or C-reactive protein level (r = 0.192). This study is the first to correlate serum SCCA level with proSPI-s. Moreover, SCCA was measured using a widely available kit. SCCA may be used to assess the severity of psoriasis.

Sections du résumé

BACKGROUND BACKGROUND
Squamous cell carcinoma antigen (SCCA) is a biomarker of disease progression in squamous cell carcinoma but also contributes to the pathogenesis of psoriasis. Eight previous studies have shown a correlation between psoriasis severity, assessed using the Psoriasis Assessment Severity Index or body surface area, and serum level of SCCA, mainly SCCA2, assessed by means of non-commercial tests. We examined the correlation between serum SCCA level, measured with a commercial kit, and psoriasis severity assessed using the Simplified Psoriasis Index (SPI).
METHODS METHODS
We conducted a prospective, non-interventional, single-centre study at the University Hospital of Tours over 18 months. The primary endpoint was same-day measurement of serum SCCA level and the psoriasis severity score on the professional version of the SPI (proSPI-s) at both baseline and follow-up. Secondary endpoints were same-day measurement of serum SCCA level and the proSPI psychosocial score (proSPI-p), proSPI treatment score, Dermatology Life Quality Index (DLQI), and inflammation parameters (C-reactive protein level, neutrophil-to-lymphocyte ratio).
RESULTS RESULTS
We included 50 psoriasis patients. Serum SCCA level was correlated with the proSPI-s at baseline and follow-up (Spearman r = 0.686 and r = 0.674, p < 0.0001) for both. It was correlated with the proSPI-p and DLQI. Serum SCCA level was not correlated with either neutrophil-to-lymphocyte ratio (r = 0.083) or C-reactive protein level (r = 0.192).
CONCLUSION CONCLUSIONS
This study is the first to correlate serum SCCA level with proSPI-s. Moreover, SCCA was measured using a widely available kit. SCCA may be used to assess the severity of psoriasis.

Identifiants

pubmed: 38422600
pii: S0151-9638(24)00002-4
doi: 10.1016/j.annder.2024.103246
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103246

Informations de copyright

Copyright © 2024 Elsevier Masson SAS. All rights reserved.

Auteurs

D Henry (D)

Dermatology Department, Centre Hospitalier Régional Universitaire, Tours, France.

A Alkhars (A)

Dermatology Department, Centre Hospitalier Régional Universitaire, Tours, France.

M Samimi (M)

Dermatology Department, Centre Hospitalier Régional Universitaire, Tours, France; Laboratoire 'Biologie des Infections à Polyomavirus [Polyomavirus Infection Biology Laboratory], ISP1282 INRA, Université de Tours, Tours, France.

D Dufour (D)

Laboratoire de Médecine nucléaire in Vitro (MNIV - In Vitro Nuclear Medicine Laboratory), Centre Hospitalier Régional Universitaire, Tours, France; UMR INSERM U1253, Université de Tours, Tours, France.

L Machet (L)

Dermatology Department, Centre Hospitalier Régional Universitaire, Tours, France; UMR INSERM U1253, Université de Tours, Tours, France. Electronic address: machet@univ-tours.fr.

Classifications MeSH