Three major dimensions of human brain cortical ageing in relation to cognitive decline across the eighth decade of life

被引:27
作者
Cox, S. R. [1 ,2 ,3 ]
Harris, M. A. [4 ]
Ritchie, S. J. [5 ]
Buchanan, C. R. [1 ,2 ,3 ]
Hernandez, M. C. Valdes [1 ,3 ,6 ]
Corley, J. [1 ,2 ]
Taylor, A. M. [1 ,2 ]
Madole, J. W. [7 ]
Harris, S. E. [1 ,2 ]
Whalley, H. C. [4 ]
McIntosh, A. M. [4 ]
Russ, T. C. [1 ,4 ,6 ,8 ]
Bastin, M. E. [1 ,3 ,6 ]
Wardlaw, J. M. [1 ,3 ,6 ,9 ]
Deary, I. J. [1 ,2 ]
Tucker-Drob, E. M. [7 ]
机构
[1] Univ Edinburgh, Lothian Birth Cohorts Grp, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Dept Psychol, Edinburgh, Midlothian, Scotland
[3] Platform Sci Excellence SINAPSE Collaborat, Scottish Imaging Network, Edinburgh, Midlothian, Scotland
[4] Univ Edinburgh, Div Psychiat, Edinburgh, Midlothian, Scotland
[5] Kings Coll London, Social Genet & Dev Psychiat Ctr, London, England
[6] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland
[7] Univ Texas Austin, Dept Psychol, Austin, TX 78712 USA
[8] Univ Edinburgh, Alzheimer Scotland Dementia Res Ctr, Edinburgh, Midlothian, Scotland
[9] Univ Edinburgh, UK Dementia Res Inst, Edinburgh, Midlothian, Scotland
基金
英国惠康基金; 英国医学研究理事会; 美国国家卫生研究院;
关键词
SURFACE-BASED ANALYSIS; LOTHIAN BIRTH COHORT; ALZHEIMERS-DISEASE; EXECUTIVE FUNCTION; APOLIPOPROTEIN-E; CEREBRAL-CORTEX; AGE;
D O I
10.1038/s41380-020-00975-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 conflate information on ageing with patterns that are present throughout life. We characterised brain cortical ageing across the eighth decade of life in a longitudinal ageing cohort, at ages similar to 73, similar to 76, and similar to 79 years, with a total of 1376 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 = 0.431, p < 0.001) and in the domains of visuospatial ability (r = 0.415, p = 0.002), processing speed (r = 0.383, p < 0.001) and memory (r = 0.372, p < 0.001). 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 cognitive declines across domains. Longitudinal approaches are invaluable for distinguishing lifelong patterns of brain-behaviour associations from patterns that are specific to aging.
引用
收藏
页码:2651 / 2662
页数:12
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