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Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study

In this exploratory study, we investigate the variation in the facial skin microbiome architecture through aging and their functional association with host genetic factors in a cohort of healthy women, living in the same area and without cutaneous diseases. Notably, facial skin microbiota (SM) sampl...

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Autores principales: Russo, Edda, Di Gloria, Leandro, Cerboneschi, Matteo, Smeazzetto, Serena, Baruzzi, Gian Paolo, Romano, Francesca, Ramazzotti, Matteo, Amedei, Amedeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045008/
https://www.ncbi.nlm.nih.gov/pubmed/36979663
http://dx.doi.org/10.3390/biomedicines11030684
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author Russo, Edda
Di Gloria, Leandro
Cerboneschi, Matteo
Smeazzetto, Serena
Baruzzi, Gian Paolo
Romano, Francesca
Ramazzotti, Matteo
Amedei, Amedeo
author_facet Russo, Edda
Di Gloria, Leandro
Cerboneschi, Matteo
Smeazzetto, Serena
Baruzzi, Gian Paolo
Romano, Francesca
Ramazzotti, Matteo
Amedei, Amedeo
author_sort Russo, Edda
collection PubMed
description In this exploratory study, we investigate the variation in the facial skin microbiome architecture through aging and their functional association with host genetic factors in a cohort of healthy women, living in the same area and without cutaneous diseases. Notably, facial skin microbiota (SM) samples were collected from a cohort of 15 healthy Caucasian females, firstly divided into three age groups (younger women aged 20–35 years old; middle aged women of 36–52 years old; and older women aged 53–68 years old). Then, the recruited cohort was divided into two groups based on their facial hydration level (dry and normal skin). The facial SM revealed a different composition in the three analyzed aging groups and between normal and dry skins. The middle-aged women also revealed functional variations associated with collagen biosynthesis and oxidative stress damage repair. Otherwise, the association between selected host SNPs (single nucleotide polymorphisms) and the facial SM profile showed significant associations, suggesting a negative correlation with collagen metabolism and ROS damage protection. Finally, the composition and functionality of the facial SM seemed to affect the aging process through the two aging-correlated pathways of host ROS damage repair and collagen metabolism. Our exploratory data could be useful for future studies characterizing the structure, function, and dynamics of the SM in the aging process to design personalized therapeutic agents focusing on potential genomic targets, microbes, and their metabolites.
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spelling pubmed-100450082023-03-29 Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study Russo, Edda Di Gloria, Leandro Cerboneschi, Matteo Smeazzetto, Serena Baruzzi, Gian Paolo Romano, Francesca Ramazzotti, Matteo Amedei, Amedeo Biomedicines Article In this exploratory study, we investigate the variation in the facial skin microbiome architecture through aging and their functional association with host genetic factors in a cohort of healthy women, living in the same area and without cutaneous diseases. Notably, facial skin microbiota (SM) samples were collected from a cohort of 15 healthy Caucasian females, firstly divided into three age groups (younger women aged 20–35 years old; middle aged women of 36–52 years old; and older women aged 53–68 years old). Then, the recruited cohort was divided into two groups based on their facial hydration level (dry and normal skin). The facial SM revealed a different composition in the three analyzed aging groups and between normal and dry skins. The middle-aged women also revealed functional variations associated with collagen biosynthesis and oxidative stress damage repair. Otherwise, the association between selected host SNPs (single nucleotide polymorphisms) and the facial SM profile showed significant associations, suggesting a negative correlation with collagen metabolism and ROS damage protection. Finally, the composition and functionality of the facial SM seemed to affect the aging process through the two aging-correlated pathways of host ROS damage repair and collagen metabolism. Our exploratory data could be useful for future studies characterizing the structure, function, and dynamics of the SM in the aging process to design personalized therapeutic agents focusing on potential genomic targets, microbes, and their metabolites. MDPI 2023-02-23 /pmc/articles/PMC10045008/ /pubmed/36979663 http://dx.doi.org/10.3390/biomedicines11030684 Text en © 2023 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
Russo, Edda
Di Gloria, Leandro
Cerboneschi, Matteo
Smeazzetto, Serena
Baruzzi, Gian Paolo
Romano, Francesca
Ramazzotti, Matteo
Amedei, Amedeo
Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title_full Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title_fullStr Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title_full_unstemmed Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title_short Facial Skin Microbiome: Aging-Related Changes and Exploratory Functional Associations with Host Genetic Factors, a Pilot Study
title_sort facial skin microbiome: aging-related changes and exploratory functional associations with host genetic factors, a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045008/
https://www.ncbi.nlm.nih.gov/pubmed/36979663
http://dx.doi.org/10.3390/biomedicines11030684
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