Three major dimensions of human brain cortical ageing in relation to cognitive decline across the 8th decade of life.
Simon R Cox,
Mathew A Harris,
Stuart J. Ritchie,
Colin R. Buchanan,
Maria del Carmen Valdés Hernández,
Adele M. Taylor,
James W. Madole,
Heather C Whalley,
Andrew M McIntosh,
Tom C Russ,
Mark E Bastin,
Joanna M. Wardlaw,
Ian J Deary,
Elliot M Tucker-Drob
Posted 19 Jan 2020
bioRxiv DOI: 10.1101/2020.01.19.911420
Posted 19 Jan 2020
Different brain regions can be grouped together, based on cross-sectional correlations among their cortical characteristics; this patterning has been used to make inferences about ageing processes. However, cross-sectional brain data conflates information on ageing with patterns that are present throughout life. We characterised brain cortical ageing across the 8th decade of life in a longitudinal ageing cohort, at ages ~73, ~76, and ~79 years, with a total of 1,376 MRI scans. Volumetric changes among cortical regions of interest (ROIs) were more strongly correlated (average r = 0.805, SD = 0.252) than were cross-sectional volumes of the same ROIs (average r = 0.350, SD = 0.178). We identified a broad, cortex-wide, dimension of atrophy that explained 66% of the variance in longitudinal changes across the cortex. Our modelling also discovered more specific fronto-temporal and occipito-parietal dimensions, that were orthogonal to the general factor and together explained an additional 20% of the variance. The general factor was associated with declines in general cognitive ability (r = 0.430, p < 0.001) and in the domains of processing speed (r = 0.383, p < 0.001) and memory (r = 0.372, p < 0.001), but not with visuospatial ability (r = 0.143, p = 0.151). Individual differences in brain cortical atrophy with ageing are manifest across three broad dimensions of the cerebral cortex, the most general of which is linked with declines in both processing speed and memory. Longitudinal approaches will prove invaluable for distinguishing lifelong patterns of brain-behaviour associations from patterns that are specific to aging.
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