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
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

1258183

Informations 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.

Auteurs

Agata Bienkowska (A)

Beiersdorf AG, Research and Development, Hamburg, Germany.
Institute for Bioinformatics, University Medicine Greifswald, Greifswald, Germany.

Günter Raddatz (G)

Division of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, Heidelberg, Germany.

Jörn Söhle (J)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Boris Kristof (B)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Henry Völzke (H)

Institute for Community Medicine, SHIP/KEF, University Medicine Greifswald, Greifswald, Germany.

Stefan Gallinat (S)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Frank Lyko (F)

Division of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, Heidelberg, Germany.

Lars Kaderali (L)

Institute for Bioinformatics, University Medicine Greifswald, Greifswald, Germany.

Marc Winnefeld (M)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Elke Grönniger (E)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Cassandra Falckenhayn (C)

Beiersdorf AG, Research and Development, Hamburg, Germany.

Classifications MeSH