Cargando…

Predicting dysfunctional age-related task activations from resting-state network alterations

Alzheimer’s disease (AD) is linked to changes in fMRI task activations and fMRI resting-state functional connectivity (restFC), which can emerge early in the illness timecourse. These fMRI correlates of unhealthy aging have been studied in largely separate subfields. Taking inspiration from neural n...

Descripción completa

Detalles Bibliográficos
Autores principales: Mill, Ravi D., Gordon, Brian A., Balota, David A., Cole, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810059/
https://www.ncbi.nlm.nih.gov/pubmed/32682094
http://dx.doi.org/10.1016/j.neuroimage.2020.117167
_version_ 1783637246233018368
author Mill, Ravi D.
Gordon, Brian A.
Balota, David A.
Cole, Michael W.
author_facet Mill, Ravi D.
Gordon, Brian A.
Balota, David A.
Cole, Michael W.
author_sort Mill, Ravi D.
collection PubMed
description Alzheimer’s disease (AD) is linked to changes in fMRI task activations and fMRI resting-state functional connectivity (restFC), which can emerge early in the illness timecourse. These fMRI correlates of unhealthy aging have been studied in largely separate subfields. Taking inspiration from neural network simulations, we propose a unifying mechanism wherein restFC alterations associated with AD disrupt the flow of activations between brain regions, leading to aberrant task activations. We apply this activity flow model in a large sample of clinically normal older adults, which was segregated into healthy (low-risk) and at-risk subgroups based on established imaging (positron emission tomography amyloid) and genetic (apolipoprotein) AD risk factors. Modeling the flow of healthy activations over at-risk AD connectivity effectively transformed the healthy aged activations into unhealthy (at-risk) aged activations. This enabled reliable prediction of at-risk AD task activations, and these predicted activations were related to individual differences in task behavior. These results support activity flow over altered intrinsic functional connections as a mechanism underlying Alzheimer’s-related dysfunction, even in very early stages of the illness. Beyond these mechanistic insights, this approach raises clinical potential by enabling prediction of task activations and associated cognitive dysfunction in individuals without requiring them to perform in-scanner cognitive tasks.
format Online
Article
Text
id pubmed-7810059
institution National Center for Biotechnology Information
language English
publishDate 2020
record_format MEDLINE/PubMed
spelling pubmed-78100592021-01-15 Predicting dysfunctional age-related task activations from resting-state network alterations Mill, Ravi D. Gordon, Brian A. Balota, David A. Cole, Michael W. Neuroimage Article Alzheimer’s disease (AD) is linked to changes in fMRI task activations and fMRI resting-state functional connectivity (restFC), which can emerge early in the illness timecourse. These fMRI correlates of unhealthy aging have been studied in largely separate subfields. Taking inspiration from neural network simulations, we propose a unifying mechanism wherein restFC alterations associated with AD disrupt the flow of activations between brain regions, leading to aberrant task activations. We apply this activity flow model in a large sample of clinically normal older adults, which was segregated into healthy (low-risk) and at-risk subgroups based on established imaging (positron emission tomography amyloid) and genetic (apolipoprotein) AD risk factors. Modeling the flow of healthy activations over at-risk AD connectivity effectively transformed the healthy aged activations into unhealthy (at-risk) aged activations. This enabled reliable prediction of at-risk AD task activations, and these predicted activations were related to individual differences in task behavior. These results support activity flow over altered intrinsic functional connections as a mechanism underlying Alzheimer’s-related dysfunction, even in very early stages of the illness. Beyond these mechanistic insights, this approach raises clinical potential by enabling prediction of task activations and associated cognitive dysfunction in individuals without requiring them to perform in-scanner cognitive tasks. 2020-07-16 2020-11-01 /pmc/articles/PMC7810059/ /pubmed/32682094 http://dx.doi.org/10.1016/j.neuroimage.2020.117167 Text en This is an open access article under the CC BY-NC-ND license. (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Article
Mill, Ravi D.
Gordon, Brian A.
Balota, David A.
Cole, Michael W.
Predicting dysfunctional age-related task activations from resting-state network alterations
title Predicting dysfunctional age-related task activations from resting-state network alterations
title_full Predicting dysfunctional age-related task activations from resting-state network alterations
title_fullStr Predicting dysfunctional age-related task activations from resting-state network alterations
title_full_unstemmed Predicting dysfunctional age-related task activations from resting-state network alterations
title_short Predicting dysfunctional age-related task activations from resting-state network alterations
title_sort predicting dysfunctional age-related task activations from resting-state network alterations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810059/
https://www.ncbi.nlm.nih.gov/pubmed/32682094
http://dx.doi.org/10.1016/j.neuroimage.2020.117167
work_keys_str_mv AT millravid predictingdysfunctionalagerelatedtaskactivationsfromrestingstatenetworkalterations
AT gordonbriana predictingdysfunctionalagerelatedtaskactivationsfromrestingstatenetworkalterations
AT balotadavida predictingdysfunctionalagerelatedtaskactivationsfromrestingstatenetworkalterations
AT colemichaelw predictingdysfunctionalagerelatedtaskactivationsfromrestingstatenetworkalterations