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Connectomic analysis of Alzheimer’s disease using percolation theory
Alzheimer’s disease (AD) is a severe neurodegenerative disorder that affects a growing worldwide elderly population. Identification of brain functional biomarkers is expected to help determine preclinical stages for targeted mechanistic studies and development of therapeutic interventions to deter d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810282/ https://www.ncbi.nlm.nih.gov/pubmed/36605889 http://dx.doi.org/10.1162/netn_a_00221 |
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author | Kotlarz, Parker Nino, Juan C. Febo, Marcelo |
author_facet | Kotlarz, Parker Nino, Juan C. Febo, Marcelo |
author_sort | Kotlarz, Parker |
collection | PubMed |
description | Alzheimer’s disease (AD) is a severe neurodegenerative disorder that affects a growing worldwide elderly population. Identification of brain functional biomarkers is expected to help determine preclinical stages for targeted mechanistic studies and development of therapeutic interventions to deter disease progression. Connectomic analysis, a graph theory–based methodology used in the analysis of brain-derived connectivity matrices was used in conjunction with percolation theory targeted attack model to investigate the network effects of AD-related amyloid deposition. We used matrices derived from resting-state functional magnetic resonance imaging collected on mice with extracellular amyloidosis (TgCRND8 mice, n = 17) and control littermates (n = 17). Global, nodal, spatial, and percolation-based analysis was performed comparing AD and control mice. These data indicate a short-term compensatory response to neurodegeneration in the AD brain via a strongly connected core network with highly vulnerable or disconnected hubs. Targeted attacks demonstrated a greater vulnerability of AD brains to all types of attacks and identified progression models to mimic AD brain functional connectivity through betweenness centrality and collective influence metrics. Furthermore, both spatial analysis and percolation theory identified a key disconnect between the anterior brain of the AD mice to the rest of the brain network. |
format | Online Article Text |
id | pubmed-9810282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98102822023-01-04 Connectomic analysis of Alzheimer’s disease using percolation theory Kotlarz, Parker Nino, Juan C. Febo, Marcelo Netw Neurosci Research Article Alzheimer’s disease (AD) is a severe neurodegenerative disorder that affects a growing worldwide elderly population. Identification of brain functional biomarkers is expected to help determine preclinical stages for targeted mechanistic studies and development of therapeutic interventions to deter disease progression. Connectomic analysis, a graph theory–based methodology used in the analysis of brain-derived connectivity matrices was used in conjunction with percolation theory targeted attack model to investigate the network effects of AD-related amyloid deposition. We used matrices derived from resting-state functional magnetic resonance imaging collected on mice with extracellular amyloidosis (TgCRND8 mice, n = 17) and control littermates (n = 17). Global, nodal, spatial, and percolation-based analysis was performed comparing AD and control mice. These data indicate a short-term compensatory response to neurodegeneration in the AD brain via a strongly connected core network with highly vulnerable or disconnected hubs. Targeted attacks demonstrated a greater vulnerability of AD brains to all types of attacks and identified progression models to mimic AD brain functional connectivity through betweenness centrality and collective influence metrics. Furthermore, both spatial analysis and percolation theory identified a key disconnect between the anterior brain of the AD mice to the rest of the brain network. MIT Press 2022-02-01 /pmc/articles/PMC9810282/ /pubmed/36605889 http://dx.doi.org/10.1162/netn_a_00221 Text en © 2021 Massachusetts Institute of Technology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Kotlarz, Parker Nino, Juan C. Febo, Marcelo Connectomic analysis of Alzheimer’s disease using percolation theory |
title | Connectomic analysis of Alzheimer’s disease using percolation theory |
title_full | Connectomic analysis of Alzheimer’s disease using percolation theory |
title_fullStr | Connectomic analysis of Alzheimer’s disease using percolation theory |
title_full_unstemmed | Connectomic analysis of Alzheimer’s disease using percolation theory |
title_short | Connectomic analysis of Alzheimer’s disease using percolation theory |
title_sort | connectomic analysis of alzheimer’s disease using percolation theory |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810282/ https://www.ncbi.nlm.nih.gov/pubmed/36605889 http://dx.doi.org/10.1162/netn_a_00221 |
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