The interplay of age, gender and amyloid on brain and cognition in mid-life and older adults

Deficits in memory are seen as a canonical sign of aging and a prodrome to dementia in older adults. However, our understanding of age-related cognition and brain morphology occurring throughout a broader spectrum of adulthood remains limited. We quantified the relationship between cognitive function and brain morphology (sulcal width, SW) using three cross-sectional observational datasets (PISA, AIBL, ADNI) from mid-life to older adulthood, assessing the influence of age, sex, amyloid (Aβ) and genetic risk for dementia. The data comprised cognitive, genetic and neuroimaging measures of a total of 1570 non-clinical mid-life and older adults (mean age 72, range 49-90 years, 1330 males) and 1365 age- and sex-matched adults with mild cognitive impairment (MCI) or Alzheimer's disease (AD). Among non-clinical adults, we found robust modes of co-variation between regional SW and multidomain cognitive function that differed between the mid-life and older age range. These cortical and cognitive profiles derived from healthy cohorts predicted out-of-sample AD and MCI. Furthermore, Aβ-deposition and educational attainment levels were associated with cognition but not SW. These findings underscoring the complex interplay between factors influencing cognition and brain structure from mid-life onwards, providing valuable insights for future research into neurodegeneration and the development of future screening algorithms.

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Publication Details

Journal
Scientific Reports
Published
2024-11-08
DOI
https://doi.org/10.1038/s41598-024-78308-3
Citations
4
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
1.54

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article

The interplay of age, gender and amyloid on brain and cognition in mid-life and older adults

Michelle K. Lupton, Anna Behler, Jürgen Fripp, Joseph Giorgio et al.
4 citations
Scientific Reports
Dementia and Cognitive Impairment Research
1.54
article

The interplay of age, gender and amyloid on brain and cognition in mid-life and older adults

Michelle K. Lupton, Anna Behler, Jürgen Fripp, Joseph Giorgio, Robert Adam, Léonie Borne, Pierrick Bourgeat, Colin Louis Masters, Gail Robinson, Paul T. Maruff, Michael Breakspear, Amelia Ceslis, Philip Mosley, Renate Thienel, Christine C. Guo, Amir Fazlollahi, Christopher C. Rowe
article en
4 citations

Abstract

Deficits in memory are seen as a canonical sign of aging and a prodrome to dementia in older adults. However, our understanding of age-related cognition and brain morphology occurring throughout a broader spectrum of adulthood remains limited. We quantified the relationship between cognitive function and brain morphology (sulcal width, SW) using three cross-sectional observational datasets (PISA, AIBL, ADNI) from mid-life to older adulthood, assessing the influence of age, sex, amyloid (Aβ) and genetic risk for dementia. The data comprised cognitive, genetic and neuroimaging measures of a total of 1570 non-clinical mid-life and older adults (mean age 72, range 49-90 years, 1330 males) and 1365 age- and sex-matched adults with mild cognitive impairment (MCI) or Alzheimer's disease (AD). Among non-clinical adults, we found robust modes of co-variation between regional SW and multidomain cognitive function that differed between the mid-life and older age range. These cortical and cognitive profiles derived from healthy cohorts predicted out-of-sample AD and MCI. Furthermore, Aβ-deposition and educational attainment levels were associated with cognition but not SW. These findings underscoring the complex interplay between factors influencing cognition and brain structure from mid-life onwards, providing valuable insights for future research into neurodegeneration and the development of future screening algorithms.

Scientific ReportsVol. 14(1)
The University of Queensland (AU), The University of Melbourne (AU), QIMR Berghofer Medical Research Institute (AU), Florey Institute of Neuroscience and Mental Health (AU), CSIRO Health and Biosecurity (AU), Austin Health (AU), University of Newcastle Australia (AU), University of California, Berkeley (US)
U.S. Department of Defense, Alzheimer's Association, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Biogen, Meso Scale Diagnostics, Alzheimer's Disease Neuroimaging Initiative, BioClinica, Novartis Pharmaceuticals Corporation, Eisai, Servier, H. Lundbeck A/S, IXICO, National Institutes of Health, Genentech, Medical Research Council, National Health and Medical Research Council
Quality Education
Openalex Percentile: Top 16%
Dementia and Cognitive Impairment Research
1.54
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