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Barrier function and microbiotic dysbiosis in atopic dermatitis

Atopic dermatitis (AD) or atopic eczema is the common inflammatory skin disorder, the prevalence of which has considerably increased during the last 30 years. It affects 15%–30% of children and 2%–10% of adults. AD characteristically alternates between periods of exacerbation or flares and periods o...

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Autores principales: Seite, Sophie, Bieber, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576901/
https://www.ncbi.nlm.nih.gov/pubmed/26396539
http://dx.doi.org/10.2147/CCID.S91521
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author Seite, Sophie
Bieber, Thomas
author_facet Seite, Sophie
Bieber, Thomas
author_sort Seite, Sophie
collection PubMed
description Atopic dermatitis (AD) or atopic eczema is the common inflammatory skin disorder, the prevalence of which has considerably increased during the last 30 years. It affects 15%–30% of children and 2%–10% of adults. AD characteristically alternates between periods of exacerbation or flares and periods of remission, which may be therapeutically induced or spontaneous. Current knowledge about AD includes abnormalities of the skin barrier (physical and chemical), the immune barrier, and more recently, the microbial barrier or microbiota. There is growing evidence for a tight relationship between them. To obtain satisfactory control of this condition, the clinical strategy to manage AD involves prescribing both anti-inflammatory medications and dermocosmetic products. The role of the physician is therefore to advise the patient with regard to hygiene measures aimed to help to improve these three barriers or to prevent any further deterioration.
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spelling pubmed-45769012015-09-22 Barrier function and microbiotic dysbiosis in atopic dermatitis Seite, Sophie Bieber, Thomas Clin Cosmet Investig Dermatol Expert Opinion Atopic dermatitis (AD) or atopic eczema is the common inflammatory skin disorder, the prevalence of which has considerably increased during the last 30 years. It affects 15%–30% of children and 2%–10% of adults. AD characteristically alternates between periods of exacerbation or flares and periods of remission, which may be therapeutically induced or spontaneous. Current knowledge about AD includes abnormalities of the skin barrier (physical and chemical), the immune barrier, and more recently, the microbial barrier or microbiota. There is growing evidence for a tight relationship between them. To obtain satisfactory control of this condition, the clinical strategy to manage AD involves prescribing both anti-inflammatory medications and dermocosmetic products. The role of the physician is therefore to advise the patient with regard to hygiene measures aimed to help to improve these three barriers or to prevent any further deterioration. Dove Medical Press 2015-09-15 /pmc/articles/PMC4576901/ /pubmed/26396539 http://dx.doi.org/10.2147/CCID.S91521 Text en © 2015 Seite and Bieber. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Expert Opinion
Seite, Sophie
Bieber, Thomas
Barrier function and microbiotic dysbiosis in atopic dermatitis
title Barrier function and microbiotic dysbiosis in atopic dermatitis
title_full Barrier function and microbiotic dysbiosis in atopic dermatitis
title_fullStr Barrier function and microbiotic dysbiosis in atopic dermatitis
title_full_unstemmed Barrier function and microbiotic dysbiosis in atopic dermatitis
title_short Barrier function and microbiotic dysbiosis in atopic dermatitis
title_sort barrier function and microbiotic dysbiosis in atopic dermatitis
topic Expert Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576901/
https://www.ncbi.nlm.nih.gov/pubmed/26396539
http://dx.doi.org/10.2147/CCID.S91521
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