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The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study

BACKGROUND: Photodynamic therapy (PDT) is an effective treatment for actinic keratosis (AKs), but there is little information on how PDT affects skin barrier function. The objectives of this study are: To compare skin barrier function between skin with AKs and healthy skin and to evaluate the impact...

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Autores principales: Soto‐Moreno, Alberto, Montero‐Vilchez, Trinidad, Diaz‐Calvillo, Pablo, Molina‐Leyva, Alejandro, Arias‐Santiago, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684974/
https://www.ncbi.nlm.nih.gov/pubmed/38017667
http://dx.doi.org/10.1111/srt.13493
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author Soto‐Moreno, Alberto
Montero‐Vilchez, Trinidad
Diaz‐Calvillo, Pablo
Molina‐Leyva, Alejandro
Arias‐Santiago, Salvador
author_facet Soto‐Moreno, Alberto
Montero‐Vilchez, Trinidad
Diaz‐Calvillo, Pablo
Molina‐Leyva, Alejandro
Arias‐Santiago, Salvador
author_sort Soto‐Moreno, Alberto
collection PubMed
description BACKGROUND: Photodynamic therapy (PDT) is an effective treatment for actinic keratosis (AKs), but there is little information on how PDT affects skin barrier function. The objectives of this study are: To compare skin barrier function between skin with AKs and healthy skin and to evaluate the impact of PDT on skin homeostasis in patients with AKs. METHODS: A prospective observational study was conducted in patients with AKs to evaluate epidermal barrier function and skin homeostasis before and 1 ek after receiving PDT. RESULTS: A total of 21 subjects were included in the study, male/female ratio was 17:4, mean age was 75.86 years. The number of AKS observed before starting treatment was reduced with respect to those diagnosed 1 month after starting PDT (14.83 vs. 1.91, p < 0.0001). Application of PDT for treating AKs modifies epidermal barrier function. Immediately after the first session temperature, transepidermal water loss (TEWL), stratum corneum hydration (SCH) and total antioxidant capacity (TAC) increased while pH decreased on lesional skin. After 1‐month follow‐up, the only remained change was the increased in SCH. Higher increases in temperature were observed when using occlusive PDT compared to mixed modality. 5‐ALA and M‐ALA seem to have a similar impact on skin barrier. CONCLUSIONS: PDT can improve skin barrier function in patients with AKs. Skin homeostasis parameters can be used to assess efficacy and optimize dosing.
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spelling pubmed-106849742023-11-30 The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study Soto‐Moreno, Alberto Montero‐Vilchez, Trinidad Diaz‐Calvillo, Pablo Molina‐Leyva, Alejandro Arias‐Santiago, Salvador Skin Res Technol Original Articles BACKGROUND: Photodynamic therapy (PDT) is an effective treatment for actinic keratosis (AKs), but there is little information on how PDT affects skin barrier function. The objectives of this study are: To compare skin barrier function between skin with AKs and healthy skin and to evaluate the impact of PDT on skin homeostasis in patients with AKs. METHODS: A prospective observational study was conducted in patients with AKs to evaluate epidermal barrier function and skin homeostasis before and 1 ek after receiving PDT. RESULTS: A total of 21 subjects were included in the study, male/female ratio was 17:4, mean age was 75.86 years. The number of AKS observed before starting treatment was reduced with respect to those diagnosed 1 month after starting PDT (14.83 vs. 1.91, p < 0.0001). Application of PDT for treating AKs modifies epidermal barrier function. Immediately after the first session temperature, transepidermal water loss (TEWL), stratum corneum hydration (SCH) and total antioxidant capacity (TAC) increased while pH decreased on lesional skin. After 1‐month follow‐up, the only remained change was the increased in SCH. Higher increases in temperature were observed when using occlusive PDT compared to mixed modality. 5‐ALA and M‐ALA seem to have a similar impact on skin barrier. CONCLUSIONS: PDT can improve skin barrier function in patients with AKs. Skin homeostasis parameters can be used to assess efficacy and optimize dosing. John Wiley and Sons Inc. 2023-11-28 /pmc/articles/PMC10684974/ /pubmed/38017667 http://dx.doi.org/10.1111/srt.13493 Text en © 2023 The Authors. Skin Research and Technology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Soto‐Moreno, Alberto
Montero‐Vilchez, Trinidad
Diaz‐Calvillo, Pablo
Molina‐Leyva, Alejandro
Arias‐Santiago, Salvador
The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title_full The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title_fullStr The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title_full_unstemmed The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title_short The impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: A prospective observational study
title_sort impact of photodynamic therapy on skin homeostasis in patients with actinic keratosis: a prospective observational study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684974/
https://www.ncbi.nlm.nih.gov/pubmed/38017667
http://dx.doi.org/10.1111/srt.13493
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