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The poly-omics of ageing through individual-based metabolic modelling
Elisabeth Yaneske1, Claudio Angione2
1Department of Computer Science and Information Systems, Teesside University, Borough Road, Middlesbrough, UK. e.yaneske@tees.ac.uk.
This study introduces a novel metabolic age predictor to better understand biological ageing. By integrating gene expression with metabolic models, it offers deeper insights into cellular ageing mechanisms beyond chronological age.
Area of Science:
- Molecular Biology
- Systems Biology
- Computational Biology
Background:
- Ageing is classified as chronological (time since birth) or biological (environmental impact on gene expression).
- Transcriptomic ageing, a measure of biological ageing, is linked to specific genes and their expression levels.
- Current transcriptomic age predictors lack insight into metabolic and cellular phenotype changes.
Purpose of the Study:
- To develop a novel method for understanding transcriptomic ageing.
- To integrate gene expression data with metabolic models for a comprehensive analysis.
- To create a new metabolic age predictor.
Main Methods:
- Utilized poly-omic constraint-based models and machine learning.
- Created individual metabolic models from normalized CD4 T-cell gene expression data (n=499).
- Combined metabolic models with transcriptomic and chronological age predictors.
Main Results:
- Developed a novel metabolic age predictor.
- Provided new insights into the differences between transcriptomic and chronological ageing.
- Demonstrated the utility of poly-omic predictors in analyzing ageing.
Conclusions:
- Poly-omic predictors offer a more detailed analysis of transcriptomic ageing than gene-based methods.
- The developed approach provides a foundation for advancing the study of human cellular ageing mechanisms.
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