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Associations among amyloid status, age, and longitudinal regional brain atrophy in cognitively unimpaired older adults.


ABSTRACT: The goal of this study was to compare regional brain atrophy patterns in cognitively unimpaired (CU) older adults with and without brain accumulation of amyloid-? (A?) to elucidate contributions of A?, age, and other variables to atrophy rates. In 80 CU participants from the Alzheimer's Disease Neuroimaging Initiative, we determined effects of A? and age on longitudinal, regional atrophy rates, while accounting for confounding variables including sex, APOE ?4 genotype, white matter lesions, and cerebrospinal fluid total and phosphorylated tau levels. We not only found overlapping patterns of atrophy in A?+ versus A?- participants but also identified regions where atrophy pattern differed between the 2 groups. Higher A? load was associated with increased longitudinal atrophy in the entorhinal cortex, amygdala, and hippocampus, even when accounting for age and other variables. Age was associated with atrophy in insula, fusiform gyrus, and isthmus cingulate, even when accounting for A?. We found age by A? interactions in the postcentral gyrus and lateral orbitofrontal cortex. These results elucidate the separate and related effects of age, A?, and other important variables on longitudinal brain atrophy rates in CU older adults.

SUBMITTER: Nosheny RL 

PROVIDER: S-EPMC7198229 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Associations among amyloid status, age, and longitudinal regional brain atrophy in cognitively unimpaired older adults.

Nosheny Rachel L RL   Insel Philip S PS   Mattsson Niklas N   Tosun Duygu D   Buckley Shannon S   Truran Diana D   Schuff N N   Aisen Paul S PS   Weiner Michael W MW  

Neurobiology of aging 20190722


The goal of this study was to compare regional brain atrophy patterns in cognitively unimpaired (CU) older adults with and without brain accumulation of amyloid-β (Aβ) to elucidate contributions of Aβ, age, and other variables to atrophy rates. In 80 CU participants from the Alzheimer's Disease Neuroimaging Initiative, we determined effects of Aβ and age on longitudinal, regional atrophy rates, while accounting for confounding variables including sex, APOE ε4 genotype, white matter lesions, and  ...[more]

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