Development of an epigenetic clock to predict visual age progression of human skin.
DNA methylation
age progression
aging
biological age
epigenetic age clock
skin aging
visual age
wrinkles
Journal
Frontiers in aging
ISSN: 2673-6217
Titre abrégé: Front Aging
Pays: Switzerland
ID NLM: 9918231199706676
Informations de publication
Date de publication:
2023
2023
Historique:
received:
13
07
2023
accepted:
28
11
2023
medline:
26
1
2024
pubmed:
26
1
2024
entrez:
26
1
2024
Statut:
epublish
Résumé
Aging is a complex process characterized by the gradual decline of physiological functions, leading to increased vulnerability to age-related diseases and reduced quality of life. Alterations in DNA methylation (DNAm) patterns have emerged as a fundamental characteristic of aged human skin, closely linked to the development of the well-known skin aging phenotype. These changes have been correlated with dysregulated gene expression and impaired tissue functionality. In particular, the skin, with its visible manifestations of aging, provides a unique model to study the aging process. Despite the importance of epigenetic age clocks in estimating biological age based on the correlation between methylation patterns and chronological age, a second-generation epigenetic age clock, which correlates DNAm patterns with a particular phenotype, specifically tailored to skin tissue is still lacking. In light of this gap, we aimed to develop a novel second-generation epigenetic age clock explicitly designed for skin tissue to facilitate a deeper understanding of the factors contributing to individual variations in age progression. To achieve this, we used methylation patterns from more than 370 female volunteers and developed the first skin-specific second-generation epigenetic age clock that accurately predicts the skin aging phenotype represented by wrinkle grade, visual facial age, and visual age progression, respectively. We then validated the performance of our clocks on independent datasets and demonstrated their broad applicability. In addition, we integrated gene expression and methylation data from independent studies to identify potential pathways contributing to skin age progression. Our results demonstrate that our epigenetic age clock, VisAgeX, specifically predicting visual age progression, not only captures known biological pathways associated with skin aging, but also adds novel pathways associated with skin aging.
Identifiants
pubmed: 38274286
doi: 10.3389/fragi.2023.1258183
pii: 1258183
pmc: PMC10809641
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1258183Informations de copyright
Copyright © 2024 Bienkowska, Raddatz, Söhle, Kristof, Völzke, Gallinat, Lyko, Kaderali, Winnefeld, Grönniger and Falckenhayn.
Déclaration de conflit d'intérêts
Authors AB, JS, BK, SG, MW, EG, and CF are employed by Beiersdorf AG. FL and LK received consultation fees from Beiersdorf AG. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.