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Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances

OBJECTIVES: This study aimed to investigate local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances (ADSD) and those without sleep disturbances (ADNSD). METHODS: Thirty eight mild AD patients with sleep disturbances and 21 mild AD patients without sleep...

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Autores principales: Wang, Lei, Zhu, Rui, Zhou, Xiao, Zhang, Zhiyong, Peng, Dantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619161/
https://www.ncbi.nlm.nih.gov/pubmed/37920381
http://dx.doi.org/10.3389/fnagi.2023.1269582
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author Wang, Lei
Zhu, Rui
Zhou, Xiao
Zhang, Zhiyong
Peng, Dantao
author_facet Wang, Lei
Zhu, Rui
Zhou, Xiao
Zhang, Zhiyong
Peng, Dantao
author_sort Wang, Lei
collection PubMed
description OBJECTIVES: This study aimed to investigate local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances (ADSD) and those without sleep disturbances (ADNSD). METHODS: Thirty eight mild AD patients with sleep disturbances and 21 mild AD patients without sleep disturbances participated in this study. All subjects underwent neuropsychological assessments and 3.0 Tesla magnetic resonance scanning. Static and dynamic regional homogeneity (ReHo) were used to represent the local functional connectivity. Seed-based whole-brain functional connectivity was used to represent the remote functional connectivity. The seed was chosen based on the results of ReHo. RESULTS: Compared to ADNSD, ADSD showed decreased static ReHo in the left posterior central gyrus and the right cuneus and increased dynamic ReHo in the left posterior central gyrus. As for the remote functional connectivity, comparing ADSD to ADNSD, it was found that there was a decreased functional connection between the left posterior central gyrus and the left cuneus as well as the left calcarine. CONCLUSION: The current study demonstrated that, compared with ADNSD, ADSD is impaired in both local and remote functional connectivity, manifested as reduced functional connectivity involving the primary sensory network and the primary visual network. The abnormality of the above functional connectivity is one of the reasons why sleep disorders promote cognitive impairment in AD. Moreover, sleep disorders change the temporal sequence of AD pathological damage to brain functional networks, but more evidence is needed to support this conclusion.
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spelling pubmed-106191612023-11-02 Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances Wang, Lei Zhu, Rui Zhou, Xiao Zhang, Zhiyong Peng, Dantao Front Aging Neurosci Aging Neuroscience OBJECTIVES: This study aimed to investigate local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances (ADSD) and those without sleep disturbances (ADNSD). METHODS: Thirty eight mild AD patients with sleep disturbances and 21 mild AD patients without sleep disturbances participated in this study. All subjects underwent neuropsychological assessments and 3.0 Tesla magnetic resonance scanning. Static and dynamic regional homogeneity (ReHo) were used to represent the local functional connectivity. Seed-based whole-brain functional connectivity was used to represent the remote functional connectivity. The seed was chosen based on the results of ReHo. RESULTS: Compared to ADNSD, ADSD showed decreased static ReHo in the left posterior central gyrus and the right cuneus and increased dynamic ReHo in the left posterior central gyrus. As for the remote functional connectivity, comparing ADSD to ADNSD, it was found that there was a decreased functional connection between the left posterior central gyrus and the left cuneus as well as the left calcarine. CONCLUSION: The current study demonstrated that, compared with ADNSD, ADSD is impaired in both local and remote functional connectivity, manifested as reduced functional connectivity involving the primary sensory network and the primary visual network. The abnormality of the above functional connectivity is one of the reasons why sleep disorders promote cognitive impairment in AD. Moreover, sleep disorders change the temporal sequence of AD pathological damage to brain functional networks, but more evidence is needed to support this conclusion. Frontiers Media S.A. 2023-10-18 /pmc/articles/PMC10619161/ /pubmed/37920381 http://dx.doi.org/10.3389/fnagi.2023.1269582 Text en Copyright © 2023 Wang, Zhu, Zhou, Zhang and Peng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Aging Neuroscience
Wang, Lei
Zhu, Rui
Zhou, Xiao
Zhang, Zhiyong
Peng, Dantao
Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title_full Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title_fullStr Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title_full_unstemmed Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title_short Altered local and remote functional connectivity in mild Alzheimer’s disease patients with sleep disturbances
title_sort altered local and remote functional connectivity in mild alzheimer’s disease patients with sleep disturbances
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619161/
https://www.ncbi.nlm.nih.gov/pubmed/37920381
http://dx.doi.org/10.3389/fnagi.2023.1269582
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