Skip to content
Open access · OA via Europe PMC

Epigenetic aging and rejuvenation of the brain: drivers, consequences, and interventions.

Lee S, Cho S, Kim SK, Yang JH.

BMB reports · 2026

Abstract

Evolution has tuned epigenetic resilience to preserve chromatin organization, transcriptional networks, and cellular identity under relentless stress. Over time, however, all eukaryotic life faces an inevitable rise in entropy that erodes the chromatin landscape at the genomic scale. This entropic decay of epigenetic information, epigenetic aging, is a primary driver of biological aging and systemic dysfunction. The brain is particularly vulnerable to epigenetic aging, with post-mitotic neurons accumulating lifelong chromatin erosion, and the glial epigenome drifting toward pro-inflammatory states. Defining the drivers and consequences of epigenetic aging in the brain forms the basis for restoring youthful chromatin landscapes, cellular identity, and cognitive capacity. [BMB Reports 2026; 59(1): 27-39].

◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:

Read at source →

Provenance

Source
Europe PMC
Canonical
link ↗
Fetched
2026-07-01 MST

Cite this

APA
S, L., S, C., SK, K., &amp; JH., Y. (2026). Epigenetic aging and rejuvenation of the brain: drivers, consequences, and interventions. <em>BMB reports</em>. https://europepmc.org/article/MED/41521073
Vancouver
S L, S C, SK K, JH. Y. Epigenetic aging and rejuvenation of the brain: drivers, consequences, and interventions. BMB reports. 2026.
BibTeX
@article{lee2026Epigen, title = {Epigenetic aging and rejuvenation of the brain: drivers, consequences, and interventions.}, author = {Lee S and Cho S and Kim SK and Yang JH.}, journal = {BMB reports}, year = {2026}, }

Research neighborhood

References, citing works, and semantically nearest findings. Click a node to open it.

Related findings