Utility of DNA Methylation as a Biomarker in Aging and Alzheimer’s Disease

Author:

Milicic Lidija123,Porter Tenielle1234,Vacher Michael15,Laws Simon M.1234

Affiliation:

1. Centre for Precision Health, Edith Cowan University, Joondalup, Western Australia, Australia

2. Collaborative Genomics and Translation Group, Edith Cowan University, Joondalup, Western Australia, Australia

3. School of Medical and Health Sciences, Edith Cowan University, Joondalup, Western Australia, Australia

4. Curtin Medical School, Curtin University, Bentley, Western Australia, Australia

5. CSIRO Health and Biosecurity, Australian e-Health Research Centre, Floreat, Western Australia

Abstract

Epigenetic mechanisms such as DNA methylation have been implicated in a number of diseases including cancer, heart disease, autoimmune disorders, and neurodegenerative diseases. While it is recognized that DNA methylation is tissue-specific, a limitation for many studies is the ability to sample the tissue of interest, which is why there is a need for a proxy tissue such as blood, that is reflective of the methylation state of the target tissue. In the last decade, DNA methylation has been utilized in the design of epigenetic clocks, which aim to predict an individual’s biological age based on an algorithmically defined set of CpGs. A number of studies have found associations between disease and/or disease risk with increased biological age, adding weight to the theory of increased biological age being linked with disease processes. Hence, this review takes a closer look at the utility of DNA methylation as a biomarker in aging and disease, with a particular focus on Alzheimer’s disease.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Neuroscience

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Editorial: DNA repair and interventions in aging;Frontiers in Aging;2023-12-05

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