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Cited 36 time in webofscience Cited 34 time in scopus
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Accelerated functional brain aging in pre-clinical familial Alzheimer's diseaseopen access

Authors
Gonneaud, JulieBaria, Alex T.Binette, Alexa PichetGordon, Brian A.Chhatwal, Jasmeer P.Cruchaga, CarlosJucker, MathiasLevin, JohannesSalloway, StephenFarlow, MartinGauthier, SergeBenzinger, Tammie L. S.Morris, John C.Bateman, Randall J.Breitner, John C. S.Poirier, JudesVachon-Presseau, EtienneVilleneuve, SylviaAlzheimer’s Disease Neuroimaging InitiativeDominantly Inherited Alzheimer Network Study GroupPre-symptomatic Evaluation of Experimental or Novel Treatments for Alzheimer’s Disease Research GrouRoh, Jee Hoon (DIAN)
Issue Date
Sep-2021
Publisher
Nature Publishing Group
Citation
Nature Communications, v.12, no.1
Indexed
SCIE
SCOPUS
Journal Title
Nature Communications
Volume
12
Number
1
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/61092
DOI
10.1038/s41467-021-25492-9
ISSN
2041-1723
Abstract
Alzheimer's disease has been associated with increased structural brain aging. Here the authors describe a model that predicts brain aging from resting state functional connectivity data, and demonstrate this is accelerated in individuals with pre-clinical familial Alzheimer's disease. Resting state functional connectivity (rs-fMRI) is impaired early in persons who subsequently develop Alzheimer's disease (AD) dementia. This impairment may be leveraged to aid investigation of the pre-clinical phase of AD. We developed a model that predicts brain age from resting state (rs)-fMRI data, and assessed whether genetic determinants of AD, as well as beta-amyloid (A beta) pathology, can accelerate brain aging. Using data from 1340 cognitively unimpaired participants between 18-94 years of age from multiple sites, we showed that topological properties of graphs constructed from rs-fMRI can predict chronological age across the lifespan. Application of our predictive model to the context of pre-clinical AD revealed that the pre-symptomatic phase of autosomal dominant AD includes acceleration of functional brain aging. This association was stronger in individuals having significant A beta pathology.
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