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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.
Afiliação
  • Russo E; Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
  • Di Gloria L; Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
  • Cerboneschi M; Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence, 50134 Florence, Italy.
  • Smeazzetto S; NEXT Genomics Srl, Sesto Fiorentino, 50019 Florence, Italy.
  • Baruzzi GP; NEXT Genomics Srl, Sesto Fiorentino, 50019 Florence, Italy.
  • Romano F; NEXT Genomics Srl, Sesto Fiorentino, 50019 Florence, Italy.
  • Ramazzotti M; Department of General Laboratory, Careggi University Hospital, 50134 Firenze, Italy.
  • Amedei A; Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence, 50134 Florence, Italy.
Biomedicines ; 11(3)2023 Feb 23.
Article em En | MEDLINE | ID: mdl-36979663
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article