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Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study

Epidermal barrier dysfunction plays an important role in atopic dermatitis (AD). The difficulty of objectively assessing AD severity and the introduction of new biologicals into clinical practice highlight the need to find parameters to monitor clinical outcomes. The aim of this study is to evaluate...

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Autores principales: Montero-Vilchez, Trinidad, Rodriguez-Pozo, Juan-Angel, Diaz-Calvillo, Pablo, Salazar-Nievas, Maria, Tercedor-Sanchez, Jesús, Molina-Leyva, Alejandro, Arias-Santiago, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225017/
https://www.ncbi.nlm.nih.gov/pubmed/35743415
http://dx.doi.org/10.3390/jcm11123341
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author Montero-Vilchez, Trinidad
Rodriguez-Pozo, Juan-Angel
Diaz-Calvillo, Pablo
Salazar-Nievas, Maria
Tercedor-Sanchez, Jesús
Molina-Leyva, Alejandro
Arias-Santiago, Salvador
author_facet Montero-Vilchez, Trinidad
Rodriguez-Pozo, Juan-Angel
Diaz-Calvillo, Pablo
Salazar-Nievas, Maria
Tercedor-Sanchez, Jesús
Molina-Leyva, Alejandro
Arias-Santiago, Salvador
author_sort Montero-Vilchez, Trinidad
collection PubMed
description Epidermal barrier dysfunction plays an important role in atopic dermatitis (AD). The difficulty of objectively assessing AD severity and the introduction of new biologicals into clinical practice highlight the need to find parameters to monitor clinical outcomes. The aim of this study is to evaluate the impact of dupilumab on skin barrier function and compare it with other treatments in patients with AD. A prospective observational study was conducted in adults with AD treated with topical corticosteroids (TCS), cyclosporine, or dupilumab. The main outcome measures after 16 weeks of treatment were Eczema Area and Severity (EASI)-50 (50% improvement in EASI), and transepidermal water loss (TEWL)-50 (50% improvement in TEWL). Forty-six patients with AD were included in the study. The proportion of patients who achieved EASI-50 at week 16 was significantly higher in patients receiving dupilumab (81.8% vs. 28.6% vs. 40%, p = 0.004). In eczematous lesions, TEWL decreased in patients receiving dupilumab (31.02 vs. 12.10 g·h(−1)·m(−2), p < 0.001) and TCS (25.30 vs. 14.88 g·h(−1)·m(−2), p = 0.047). The proportion of patients who achieved TEWL-50 at week 16 was higher for dupilumab than for cyclosporine or TCS. Temperature only decreased in the dupilumab group. Stratum corneum hydration increased in eczematous lesions and non-involved skin only in patients with dupilumab. In conclusion, dupilumab improves skin barrier function in patients with AD better than TCS or cyclosporine, both in eczematous lesions and in non-lesioned skin.
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spelling pubmed-92250172022-06-24 Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study Montero-Vilchez, Trinidad Rodriguez-Pozo, Juan-Angel Diaz-Calvillo, Pablo Salazar-Nievas, Maria Tercedor-Sanchez, Jesús Molina-Leyva, Alejandro Arias-Santiago, Salvador J Clin Med Article Epidermal barrier dysfunction plays an important role in atopic dermatitis (AD). The difficulty of objectively assessing AD severity and the introduction of new biologicals into clinical practice highlight the need to find parameters to monitor clinical outcomes. The aim of this study is to evaluate the impact of dupilumab on skin barrier function and compare it with other treatments in patients with AD. A prospective observational study was conducted in adults with AD treated with topical corticosteroids (TCS), cyclosporine, or dupilumab. The main outcome measures after 16 weeks of treatment were Eczema Area and Severity (EASI)-50 (50% improvement in EASI), and transepidermal water loss (TEWL)-50 (50% improvement in TEWL). Forty-six patients with AD were included in the study. The proportion of patients who achieved EASI-50 at week 16 was significantly higher in patients receiving dupilumab (81.8% vs. 28.6% vs. 40%, p = 0.004). In eczematous lesions, TEWL decreased in patients receiving dupilumab (31.02 vs. 12.10 g·h(−1)·m(−2), p < 0.001) and TCS (25.30 vs. 14.88 g·h(−1)·m(−2), p = 0.047). The proportion of patients who achieved TEWL-50 at week 16 was higher for dupilumab than for cyclosporine or TCS. Temperature only decreased in the dupilumab group. Stratum corneum hydration increased in eczematous lesions and non-involved skin only in patients with dupilumab. In conclusion, dupilumab improves skin barrier function in patients with AD better than TCS or cyclosporine, both in eczematous lesions and in non-lesioned skin. MDPI 2022-06-10 /pmc/articles/PMC9225017/ /pubmed/35743415 http://dx.doi.org/10.3390/jcm11123341 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Montero-Vilchez, Trinidad
Rodriguez-Pozo, Juan-Angel
Diaz-Calvillo, Pablo
Salazar-Nievas, Maria
Tercedor-Sanchez, Jesús
Molina-Leyva, Alejandro
Arias-Santiago, Salvador
Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title_full Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title_fullStr Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title_full_unstemmed Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title_short Dupilumab Improves Skin Barrier Function in Adults with Atopic Dermatitis: A Prospective Observational Study
title_sort dupilumab improves skin barrier function in adults with atopic dermatitis: a prospective observational study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225017/
https://www.ncbi.nlm.nih.gov/pubmed/35743415
http://dx.doi.org/10.3390/jcm11123341
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