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Loss of brain inter-frequency hubs in Alzheimer's disease
Alzheimer’s disease (AD) causes alterations of brain network structure and function. The latter consists of connectivity changes between oscillatory processes at different frequency channels. We proposed a multi-layer network approach to analyze multiple-frequency brain networks inferred from magnet...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589939/ https://www.ncbi.nlm.nih.gov/pubmed/28883408 http://dx.doi.org/10.1038/s41598-017-07846-w |
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author | Guillon, J. Attal, Y. Colliot, O. La Corte, V. Dubois, B. Schwartz, D. Chavez, M. De Vico Fallani, F. |
author_facet | Guillon, J. Attal, Y. Colliot, O. La Corte, V. Dubois, B. Schwartz, D. Chavez, M. De Vico Fallani, F. |
author_sort | Guillon, J. |
collection | PubMed |
description | Alzheimer’s disease (AD) causes alterations of brain network structure and function. The latter consists of connectivity changes between oscillatory processes at different frequency channels. We proposed a multi-layer network approach to analyze multiple-frequency brain networks inferred from magnetoencephalographic recordings during resting-states in AD subjects and age-matched controls. Main results showed that brain networks tend to facilitate information propagation across different frequencies, as measured by the multi-participation coefficient (MPC). However, regional connectivity in AD subjects was abnormally distributed across frequency bands as compared to controls, causing significant decreases of MPC. This effect was mainly localized in association areas and in the cingulate cortex, which acted, in the healthy group, as a true inter-frequency hub. MPC values significantly correlated with memory impairment of AD subjects, as measured by the total recall score. Most predictive regions belonged to components of the default-mode network that are typically affected by atrophy, metabolism disruption and amyloid-β deposition. We evaluated the diagnostic power of the MPC and we showed that it led to increased classification accuracy (78.39%) and sensitivity (91.11%). These findings shed new light on the brain functional alterations underlying AD and provide analytical tools for identifying multi-frequency neural mechanisms of brain diseases. |
format | Online Article Text |
id | pubmed-5589939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55899392017-09-13 Loss of brain inter-frequency hubs in Alzheimer's disease Guillon, J. Attal, Y. Colliot, O. La Corte, V. Dubois, B. Schwartz, D. Chavez, M. De Vico Fallani, F. Sci Rep Article Alzheimer’s disease (AD) causes alterations of brain network structure and function. The latter consists of connectivity changes between oscillatory processes at different frequency channels. We proposed a multi-layer network approach to analyze multiple-frequency brain networks inferred from magnetoencephalographic recordings during resting-states in AD subjects and age-matched controls. Main results showed that brain networks tend to facilitate information propagation across different frequencies, as measured by the multi-participation coefficient (MPC). However, regional connectivity in AD subjects was abnormally distributed across frequency bands as compared to controls, causing significant decreases of MPC. This effect was mainly localized in association areas and in the cingulate cortex, which acted, in the healthy group, as a true inter-frequency hub. MPC values significantly correlated with memory impairment of AD subjects, as measured by the total recall score. Most predictive regions belonged to components of the default-mode network that are typically affected by atrophy, metabolism disruption and amyloid-β deposition. We evaluated the diagnostic power of the MPC and we showed that it led to increased classification accuracy (78.39%) and sensitivity (91.11%). These findings shed new light on the brain functional alterations underlying AD and provide analytical tools for identifying multi-frequency neural mechanisms of brain diseases. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589939/ /pubmed/28883408 http://dx.doi.org/10.1038/s41598-017-07846-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guillon, J. Attal, Y. Colliot, O. La Corte, V. Dubois, B. Schwartz, D. Chavez, M. De Vico Fallani, F. Loss of brain inter-frequency hubs in Alzheimer's disease |
title | Loss of brain inter-frequency hubs in Alzheimer's disease |
title_full | Loss of brain inter-frequency hubs in Alzheimer's disease |
title_fullStr | Loss of brain inter-frequency hubs in Alzheimer's disease |
title_full_unstemmed | Loss of brain inter-frequency hubs in Alzheimer's disease |
title_short | Loss of brain inter-frequency hubs in Alzheimer's disease |
title_sort | loss of brain inter-frequency hubs in alzheimer's disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589939/ https://www.ncbi.nlm.nih.gov/pubmed/28883408 http://dx.doi.org/10.1038/s41598-017-07846-w |
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