Distinct lifespan trajectories of cortical intrinsic timescales and neural oscillations
- 1McGill University
Abstract
The brain integrates information over time through the persistence of neural activity, yet how this persistence changes across the human lifespan and the mechanisms underlying these changes remain unclear. Using resting-state magnetoencephalography from three independent cohorts (n = 1,156; ages 6-88 years), we systematically examined lifespan changes in neural temporal dynamics, focusing on cortical intrinsic timescales and alpha oscillatory frequency. We found that cortical intrinsic timescales shortened from approximately 29 ms in childhood to 9 ms in late adulthood, with the steepest decline occurring before age 30. This compression was reproducible across cohorts and observed in all cortical regions, while the sensory-to-association hierarchy of timescales remained preserved throughout life. By contrast, alpha frequency followed a distinct trajectory, peaking in early adulthood before declining after midlife. Individualized corticothalamic models linked timescale compression to stronger intrathalamic inhibition, whereas increased conduction delays partly accounted for alpha slowing. Further network simulations indicated that intrinsic timescales primarily reflect collective network dynamics rather than single-neuron kinetics. Together, these findings reveal distinct lifespan trajectories of neural persistence and oscillatory rhythms, implicating collective corticothalamic dynamics in the temporal organization of the human brain across development and ageing.
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BibTeX
@misc{liu2026distinct,
title = {{Distinct lifespan trajectories of cortical intrinsic timescales and neural oscillations}},
author = {X. Liu and B. Harris and R. Lu and S. Wang and Q. Yu and M. Zhang and R. Cui and X. Liang and T. Fan},
howpublished = {bioRxiv},
year = {2026},
month = nov,
doi = {10.64898/2026.11.04.764097},
url = {https://www.biorxiv.org/content/10.64898/2026.11.04.764097v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Distinct lifespan trajectories of cortical intrinsic timescales and neural oscillations
AU - X. Liu
AU - B. Harris
AU - R. Lu
AU - S. Wang
AU - Q. Yu
AU - M. Zhang
AU - R. Cui
AU - X. Liang
AU - T. Fan
PY - 2026
DA - 2026/11/04
PB - bioRxiv
DO - 10.64898/2026.11.04.764097
UR - https://www.biorxiv.org/content/10.64898/2026.11.04.764097v1
AB - The brain integrates information over time through the persistence of neural activity, yet how this persistence changes across the human lifespan and the mechanisms underlying these changes remain unclear. Using resting-state magnetoencephalography from three independent cohorts (n = 1,156; ages 6-88 years), we systematically examined lifespan changes in neural temporal dynamics, focusing on cortical intrinsic timescales and alpha oscillatory frequency. We found that cortical intrinsic timescales shortened from approximately 29 ms in childhood to 9 ms in late adulthood, with the steepest decline occurring before age 30. This compression was reproducible across cohorts and observed in all cortical regions, while the sensory-to-association hierarchy of timescales remained preserved throughout life. By contrast, alpha frequency followed a distinct trajectory, peaking in early adulthood before declining after midlife. Individualized corticothalamic models linked timescale compression to stronger intrathalamic inhibition, whereas increased conduction delays partly accounted for alpha slowing. Further network simulations indicated that intrinsic timescales primarily reflect collective network dynamics rather than single-neuron kinetics. Together, these findings reveal distinct lifespan trajectories of neural persistence and oscillatory rhythms, implicating collective corticothalamic dynamics in the temporal organization of the human brain across development and ageing.
ER -