Machine Learning Classification Identifies Cerebellar Contributions to Early and Moderate Cognitive Decline in Alzheimer's Disease.

Alzheimer’s disease MCI (mild cognitive impairment) cerebellum dementia gray matter (GM) machine learning mild moderate AD white matter (WM)

Journal

Frontiers in aging neuroscience
ISSN: 1663-4365
Titre abrégé: Front Aging Neurosci
Pays: Switzerland
ID NLM: 101525824

Informations de publication

Date de publication:
2020
Historique:
received: 01 01 2020
accepted: 28 09 2020
entrez: 26 11 2020
pubmed: 27 11 2020
medline: 27 11 2020
Statut: epublish

Résumé

Alzheimer's disease (AD) is one of the most common forms of dementia, marked by progressively degrading cognitive function. Although cerebellar changes occur throughout AD progression, its involvement and predictive contribution in its earliest stages, as well as gray or white matter components involved, remains unclear. We used MRI machine learning-based classification to assess the contribution of two tissue components [volume fraction myelin (VFM), and gray matter (GM) volume] within the whole brain, the neocortex, the whole cerebellum as well as its anterior and posterior parts and their predictive contribution to the first two stages of AD and typically aging controls. While classification accuracy increased with AD stages, VFM was the best predictor for all early stages of dementia when compared with typically aging controls. However, we document overall higher cerebellar prediction accuracy when compared to the whole brain with distinct structural signatures of higher anterior cerebellar contribution to mild cognitive impairment (MCI) and higher posterior cerebellar contribution to mild/moderate stages of AD for each tissue property. Based on these different cerebellar profiles and their unique contribution to early disease stages, we propose a refined model of cerebellar contribution to early AD development.

Identifiants

pubmed: 33240072
doi: 10.3389/fnagi.2020.524024
pmc: PMC7669549
doi:

Types de publication

Journal Article

Langues

eng

Pagination

524024

Informations de copyright

Copyright © 2020 Bruchhage, Correia, Malloy, Salloway and Deoni.

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Auteurs

Muriel M K Bruchhage (MMK)

Advanced Baby Imaging Lab, Hasbro Children's Hospital, Rhode Island Hospital, Providence, RI, United States.
Department of Pediatrics, Warren Alpert Medical School at Brown University, Providence, RI, United States.

Stephen Correia (S)

Butler Hospital Memory and Aging Program, Providence, RI, United States.
Department of Human Behavior and Psychiatry, Warren Alpert Medical School at Brown University, Providence, RI, United States.

Paul Malloy (P)

Butler Hospital Memory and Aging Program, Providence, RI, United States.
Department of Human Behavior and Psychiatry, Warren Alpert Medical School at Brown University, Providence, RI, United States.

Stephen Salloway (S)

Butler Hospital Memory and Aging Program, Providence, RI, United States.
Department of Human Behavior and Psychiatry, Warren Alpert Medical School at Brown University, Providence, RI, United States.
Department of Neurology, Warren Alpert Medical School at Brown University, Providence, RI, United States.

Sean Deoni (S)

Advanced Baby Imaging Lab, Hasbro Children's Hospital, Rhode Island Hospital, Providence, RI, United States.
Department of Pediatrics, Warren Alpert Medical School at Brown University, Providence, RI, United States.
Maternal, Newborn and Child Health Discovery & Tools, Bill & Melinda Gates Foundation, Seattle, WA, United States.

Classifications MeSH