| Literature DB >> 30241605 |
Adam E Field1, Neil A Robertson2, Tina Wang3, Aaron Havas1, Trey Ideker3, Peter D Adams4.
Abstract
Age-associated changes to the mammalian DNA methylome are well documented and thought to promote diseases of aging, such as cancer. Recent studies have identified collections of individual methylation sites whose aggregate methylation status measures chronological age, referred to as the DNA methylation clock. DNA methylation may also have value as a biomarker of healthy versus unhealthy aging and disease risk; in other words, a biological clock. Here we consider the relationship between the chronological and biological clocks, their underlying mechanisms, potential consequences, and their utility as biomarkers and as targets for intervention to promote healthy aging and longevity.Entities:
Keywords: DNA methylation; aging; biological age; chronological age; clock; epigenetics
Mesh:
Year: 2018 PMID: 30241605 PMCID: PMC6520108 DOI: 10.1016/j.molcel.2018.08.008
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970