Age affects white matter microstructure and episodic memory across the older adult lifespan
•White matter microstructure varies nonlinearly across the older adult lifespan•Nonlinear effects across the brain were seen for fractional anisotropy and radial diffusivity metrics, but not axial diffusivity•Age effects are not solely due to white matter pathology or cognitive impairment•Age effect...
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Veröffentlicht in: | Neurobiology of aging 2021-10, Vol.106, p.282-291 |
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Sprache: | eng |
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Zusammenfassung: | •White matter microstructure varies nonlinearly across the older adult lifespan•Nonlinear effects across the brain were seen for fractional anisotropy and radial diffusivity metrics, but not axial diffusivity•Age effects are not solely due to white matter pathology or cognitive impairment•Age effects on episodic memory were mediated by medial temporal microstructure
Diffusion imaging studies have observed age-related degradation of white matter that contributes to cognitive deficits separately in younger-old (ages 65–89) and oldest-old (ages 90+) adults. But it remains unclear whether these age effects are magnified in advanced age groups, which may reflect disease-related pathology. Here, we tested whether age-related differences in white matter microstructure followed linear or nonlinear patterns across the entire older adult lifespan (65–98 years), these patterns were influenced by oldest-old adults at increased risk of dementia (cognitive impairment no dementia, CIND), and they explained age effects on episodic memory. Results revealed nonlinear microstructure declines across fiber classes (medial temporal, callosal, association, projection and/or thalamic) that were largest for medial temporal fibers. These patterns remained after excluding oldest-old participants with CIND, indicating that aging of white matter microstructure cannot solely be explained by pathology associated with early cognitive impairment. Moreover, finding that the effect of age on episodic memory was mediated by medial temporal fiber microstructure suggests it is essential for facilitating memory-related neural signals across the older adult lifespan. |
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ISSN: | 0197-4580 1558-1497 |
DOI: | 10.1016/j.neurobiolaging.2021.06.021 |