Deep down, we’re aging.

We publish today in Cerebral Cortex a study that advances our understanding of the effects of biological aging on the neurophysiology of deeper brain structures that are crucial to cognitive functions.

This study was driven by INSERM Principal Investigator Thomas Hinault, in collaboration with Johns-Hopkins cognitive neuroscientist Susan Courtney.

From the paper — Cognitive decline with age is associated with brain atrophy and reduced brain activations, but the underlying neurophysiological mechanisms are unclear, especially in deeper brain structures primarily affected by healthy aging or neurodegenerative processes. Here, we characterize time-resolved, resting-state magnetoencephalography activity of the hippocampus and subcortical brain regions in a large cohort of healthy young (20–30 years) and older (70–80 years) volunteers from the Cam-CAN (Cambridge Centre for Ageing and Neuroscience) open repository. The data show age-related changes in both rhythmic and arrhythmic signal strength in multiple deeper brain regions, including the hippocampus, striatum, and thalamus. We observe a slowing of neural activity across deeper brain regions, with increased delta and reduced gamma activity, which echoes previous reports of cortical slowing. We also report reduced occipito-parietal alpha peak associated with increased theta-band activity in the hippocampus, an effect that may reflect compensatory processes as theta activity, and slope of arrhythmic activity were more strongly expressed when short-term memory performances were preserved. Overall, this study advances the understanding of the biological nature of inter-individual variability in aging. The data provide new insight into how hippocampus and subcortical neurophysiological activity evolve with biological age, and highlight frequency-specific effects associated with cognitive decline versus cognitive maintenance.