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Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease

Alzheimer’s disease (AD) is a neurodegenerative disorder associated with the progressive dysfunction of cognitive ability. Previous research has indicated that the default mode network (DMN) is closely related to cognition and is impaired in Alzheimer’s disease. Because recent studies have shown tha...

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Autores principales: Li, Youjun, Yao, Hongxiang, Lin, Pan, Zheng, Liang, Li, Chenxi, Zhou, Bo, Wang, Pan, Zhang, Zengqiang, Wang, Luning, An, Ningyu, Wang, Jue, Zhang, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540901/
https://www.ncbi.nlm.nih.gov/pubmed/28824420
http://dx.doi.org/10.3389/fnagi.2017.00259
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author Li, Youjun
Yao, Hongxiang
Lin, Pan
Zheng, Liang
Li, Chenxi
Zhou, Bo
Wang, Pan
Zhang, Zengqiang
Wang, Luning
An, Ningyu
Wang, Jue
Zhang, Xi
author_facet Li, Youjun
Yao, Hongxiang
Lin, Pan
Zheng, Liang
Li, Chenxi
Zhou, Bo
Wang, Pan
Zhang, Zengqiang
Wang, Luning
An, Ningyu
Wang, Jue
Zhang, Xi
author_sort Li, Youjun
collection PubMed
description Alzheimer’s disease (AD) is a neurodegenerative disorder associated with the progressive dysfunction of cognitive ability. Previous research has indicated that the default mode network (DMN) is closely related to cognition and is impaired in Alzheimer’s disease. Because recent studies have shown that different frequency bands represent specific physiological functions, DMN functional connectivity studies of the different frequency bands based on resting state fMRI (RS-fMRI) data may provide new insight into AD pathophysiology. In this study, we explored the functional connectivity based on well-defined DMN regions of interest (ROIs) from the five frequency bands: slow-5 (0.01–0.027 Hz), slow-4 (0.027–0.073 Hz), slow-3 (0.073–0.198 Hz), slow-2 (0.198–0.25 Hzs) and standard low-frequency oscillations (LFO) (0.01–0.08 Hz). We found that the altered functional connectivity patterns are mainly in the frequency band of slow-5 and slow-4 and that the decreased connections are long distance, but some relatively short connections are increased. In addition, the altered functional connections of the DMN in AD are frequency dependent and differ between the slow-5 and slow-4 bands. Mini-Mental State Examination scores were significantly correlated with the altered functional connectivity patterns in the slow-5 and slow-4 bands. These results indicate that frequency-dependent functional connectivity changes might provide potential biomarkers for AD pathophysiology.
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spelling pubmed-55409012017-08-18 Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease Li, Youjun Yao, Hongxiang Lin, Pan Zheng, Liang Li, Chenxi Zhou, Bo Wang, Pan Zhang, Zengqiang Wang, Luning An, Ningyu Wang, Jue Zhang, Xi Front Aging Neurosci Neuroscience Alzheimer’s disease (AD) is a neurodegenerative disorder associated with the progressive dysfunction of cognitive ability. Previous research has indicated that the default mode network (DMN) is closely related to cognition and is impaired in Alzheimer’s disease. Because recent studies have shown that different frequency bands represent specific physiological functions, DMN functional connectivity studies of the different frequency bands based on resting state fMRI (RS-fMRI) data may provide new insight into AD pathophysiology. In this study, we explored the functional connectivity based on well-defined DMN regions of interest (ROIs) from the five frequency bands: slow-5 (0.01–0.027 Hz), slow-4 (0.027–0.073 Hz), slow-3 (0.073–0.198 Hz), slow-2 (0.198–0.25 Hzs) and standard low-frequency oscillations (LFO) (0.01–0.08 Hz). We found that the altered functional connectivity patterns are mainly in the frequency band of slow-5 and slow-4 and that the decreased connections are long distance, but some relatively short connections are increased. In addition, the altered functional connections of the DMN in AD are frequency dependent and differ between the slow-5 and slow-4 bands. Mini-Mental State Examination scores were significantly correlated with the altered functional connectivity patterns in the slow-5 and slow-4 bands. These results indicate that frequency-dependent functional connectivity changes might provide potential biomarkers for AD pathophysiology. Frontiers Media S.A. 2017-08-03 /pmc/articles/PMC5540901/ /pubmed/28824420 http://dx.doi.org/10.3389/fnagi.2017.00259 Text en Copyright © 2017 Li, Yao, Lin, Zheng, Li, Zhou, Wang, Zhang, Wang, An, Wang and Zhang. http://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) or licensor 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 Neuroscience
Li, Youjun
Yao, Hongxiang
Lin, Pan
Zheng, Liang
Li, Chenxi
Zhou, Bo
Wang, Pan
Zhang, Zengqiang
Wang, Luning
An, Ningyu
Wang, Jue
Zhang, Xi
Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title_full Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title_fullStr Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title_full_unstemmed Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title_short Frequency-Dependent Altered Functional Connections of Default Mode Network in Alzheimer’s Disease
title_sort frequency-dependent altered functional connections of default mode network in alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540901/
https://www.ncbi.nlm.nih.gov/pubmed/28824420
http://dx.doi.org/10.3389/fnagi.2017.00259
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