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Decoding Skin Aging Through Transcriptomic Clocks: Gene Expression Signatures, Associated Pathways, and Explainable
Vasiliki Kefala1, Vasiliki-Sofia Grech1, Niki Tertipi1
1Department of Biomedical Sciences, School of Health and Care Sciences, University of West Attica, GR-12243 Athens, Greece.
Transcriptomic aging clocks offer a dynamic way to measure skin aging beyond chronological age. These gene-expression models reveal key aging processes like senescence and inflammation.
Area of Science:
- Dermatology
- Genomics
- Computational Biology
Background:
- Skin aging is a complex process influenced by intrinsic and extrinsic factors.
- Chronological age is an insufficient measure of skin's biological aging state.
- Molecular biomarkers are needed to accurately assess skin aging variability.
Purpose of the Study:
- To review transcriptomic aging clocks in human skin.
- To emphasize gene-expression signatures, biological pathways, and computational modeling.
- To evaluate advancements in machine learning and artificial intelligence for skin aging.
Main Methods:
- Targeted literature search in PubMed and IEEE Xplore.
- Focus on gene-expression profiles and computational models.
- Analysis of transcriptomic frameworks like SkinAGE.
Main Results:
- Transcriptomic models capture coordinated changes in senescence, DNA damage, inflammation, and ECM remodeling.
- Gene-expression approaches quantify dynamic and biologically relevant skin aging states.
- Machine learning, including deep learning, enhances aging clock accuracy and interpretability.
Conclusions:
- Transcriptomic aging clocks provide dynamic and personalized insights into skin aging.
- Explainable AI is crucial for understanding and trusting these models.
- Future research will integrate multi-omics data and digital twins for predictive skin aging models.
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