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Altered functional connectivity of the default mode and frontal control networks in patients with insomnia

AIMS: The purpose of this study was to investigate the association between spontaneous regional activity and brain functional connectivity, which maybe can distinguish insomnia while being responsive to repetitive transcranial magnetic stimulation (rTMS) treatment effects in insomnia patients. METHO...

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Autores principales: Zheng, Hui, Zhou, Qin, Yang, Junjie, Lu, Qian, Qiu, Huaide, He, Chuan, Yan, Hailang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352894/
https://www.ncbi.nlm.nih.gov/pubmed/36942498
http://dx.doi.org/10.1111/cns.14183
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author Zheng, Hui
Zhou, Qin
Yang, Junjie
Lu, Qian
Qiu, Huaide
He, Chuan
Yan, Hailang
author_facet Zheng, Hui
Zhou, Qin
Yang, Junjie
Lu, Qian
Qiu, Huaide
He, Chuan
Yan, Hailang
author_sort Zheng, Hui
collection PubMed
description AIMS: The purpose of this study was to investigate the association between spontaneous regional activity and brain functional connectivity, which maybe can distinguish insomnia while being responsive to repetitive transcranial magnetic stimulation (rTMS) treatment effects in insomnia patients. METHODS: Using resting‐state functional magnetic resonance imaging data from 38 chronic insomnia patients and 36 healthy volunteers, we compared the amplitude of low‐frequency fluctuations (ALFF) between the two groups. Of all the patients with insomnia, 20 received rTMS for 4 weeks, while 18 patients received a 4‐week pseudo‐stimulation intervention. Seed‐based resting‐state functional connectivity (RSFC) analysis was conducted from regions with significantly different ALFF values, and the association between RSFC value and Pittsburgh Sleep Quality Index score was determined. RESULTS: Our results revealed that insomnia patients presented a significantly higher ALFF value in the posterior cingulate cortex (PCC), whereas a significantly lower ALFF value was observed in the superior parietal lobule (SPL). Moreover, significantly reduced RSFC was detected from both PCC to prefrontal cortex connections, as well as from left SPL to frontal pole connections. In addition, RSFC from frontal pole to left SPL negatively predicted sleep quality (PSQI) and treatment response in patients' group. CONCLUSION: Our findings suggest that disrupted frontoparietal network connectivity may be a biomarker for insomnia in middle‐aged adults, reinforcing the potential of rTMS targeting the frontal lobes. Monitoring pretreatment RSFC could offer greater insight into how rTMS treatments are responded to by insomniacs.
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spelling pubmed-103528942023-07-19 Altered functional connectivity of the default mode and frontal control networks in patients with insomnia Zheng, Hui Zhou, Qin Yang, Junjie Lu, Qian Qiu, Huaide He, Chuan Yan, Hailang CNS Neurosci Ther Original Articles AIMS: The purpose of this study was to investigate the association between spontaneous regional activity and brain functional connectivity, which maybe can distinguish insomnia while being responsive to repetitive transcranial magnetic stimulation (rTMS) treatment effects in insomnia patients. METHODS: Using resting‐state functional magnetic resonance imaging data from 38 chronic insomnia patients and 36 healthy volunteers, we compared the amplitude of low‐frequency fluctuations (ALFF) between the two groups. Of all the patients with insomnia, 20 received rTMS for 4 weeks, while 18 patients received a 4‐week pseudo‐stimulation intervention. Seed‐based resting‐state functional connectivity (RSFC) analysis was conducted from regions with significantly different ALFF values, and the association between RSFC value and Pittsburgh Sleep Quality Index score was determined. RESULTS: Our results revealed that insomnia patients presented a significantly higher ALFF value in the posterior cingulate cortex (PCC), whereas a significantly lower ALFF value was observed in the superior parietal lobule (SPL). Moreover, significantly reduced RSFC was detected from both PCC to prefrontal cortex connections, as well as from left SPL to frontal pole connections. In addition, RSFC from frontal pole to left SPL negatively predicted sleep quality (PSQI) and treatment response in patients' group. CONCLUSION: Our findings suggest that disrupted frontoparietal network connectivity may be a biomarker for insomnia in middle‐aged adults, reinforcing the potential of rTMS targeting the frontal lobes. Monitoring pretreatment RSFC could offer greater insight into how rTMS treatments are responded to by insomniacs. John Wiley and Sons Inc. 2023-03-21 /pmc/articles/PMC10352894/ /pubmed/36942498 http://dx.doi.org/10.1111/cns.14183 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zheng, Hui
Zhou, Qin
Yang, Junjie
Lu, Qian
Qiu, Huaide
He, Chuan
Yan, Hailang
Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title_full Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title_fullStr Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title_full_unstemmed Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title_short Altered functional connectivity of the default mode and frontal control networks in patients with insomnia
title_sort altered functional connectivity of the default mode and frontal control networks in patients with insomnia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352894/
https://www.ncbi.nlm.nih.gov/pubmed/36942498
http://dx.doi.org/10.1111/cns.14183
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