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Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia
Several neuroimaging studies have suggested that brain impairment and plasticity occur in patients with chronic primary insomnia (CPI); however, the effects of insomnia on the intrinsic organization of the brain remain largely unknown. In this study, a voxel-based functional connectivity strength (F...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473502/ https://www.ncbi.nlm.nih.gov/pubmed/28652745 http://dx.doi.org/10.2147/NDT.S137292 |
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author | Huang, Suhua Zhou, Fuqing Jiang, Jian Huang, Muhua Zeng, Xianjun Ding, Shan Gong, Honghan |
author_facet | Huang, Suhua Zhou, Fuqing Jiang, Jian Huang, Muhua Zeng, Xianjun Ding, Shan Gong, Honghan |
author_sort | Huang, Suhua |
collection | PubMed |
description | Several neuroimaging studies have suggested that brain impairment and plasticity occur in patients with chronic primary insomnia (CPI); however, the effects of insomnia on the intrinsic organization of the brain remain largely unknown. In this study, a voxel-based functional connectivity strength (FCS) assessment, a data-driven method based on a theoretical approach, was applied to investigate the effects of insomnia on the intrinsic organization of the whole brain in 27 treatment-naïve CPI patients and 26 well-matched healthy controls (HCs). Compared with HCs, CPI patients exhibited decreased FCS primarily in the right dorsolateral prefrontal cortex, the right medial prefrontal cortex (MPFC), the left basal ganglia/insula, and the right cerebellum anterior lobe (CAL) due to decreased functional connectivity patterns. These results suggest that poor sleep quality could impair FCS within the brain, including the MPFC and the CAL, which are important for cognitive control and modulating motor and limbic functions. Additionally, a receiver operator characteristic analysis revealed that altered FCS has moderate sensitivity (76.9%–88.5%) and specificity (59.3%–70.4%) as a reference indicator to discriminate CPI patients from HCs. Taken together, these findings provide evidence for abnormal intrinsic brain activity in CPI patients and might improve our understanding of the pathophysiological processes that occur in insomnia patients. |
format | Online Article Text |
id | pubmed-5473502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54735022017-06-26 Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia Huang, Suhua Zhou, Fuqing Jiang, Jian Huang, Muhua Zeng, Xianjun Ding, Shan Gong, Honghan Neuropsychiatr Dis Treat Original Research Several neuroimaging studies have suggested that brain impairment and plasticity occur in patients with chronic primary insomnia (CPI); however, the effects of insomnia on the intrinsic organization of the brain remain largely unknown. In this study, a voxel-based functional connectivity strength (FCS) assessment, a data-driven method based on a theoretical approach, was applied to investigate the effects of insomnia on the intrinsic organization of the whole brain in 27 treatment-naïve CPI patients and 26 well-matched healthy controls (HCs). Compared with HCs, CPI patients exhibited decreased FCS primarily in the right dorsolateral prefrontal cortex, the right medial prefrontal cortex (MPFC), the left basal ganglia/insula, and the right cerebellum anterior lobe (CAL) due to decreased functional connectivity patterns. These results suggest that poor sleep quality could impair FCS within the brain, including the MPFC and the CAL, which are important for cognitive control and modulating motor and limbic functions. Additionally, a receiver operator characteristic analysis revealed that altered FCS has moderate sensitivity (76.9%–88.5%) and specificity (59.3%–70.4%) as a reference indicator to discriminate CPI patients from HCs. Taken together, these findings provide evidence for abnormal intrinsic brain activity in CPI patients and might improve our understanding of the pathophysiological processes that occur in insomnia patients. Dove Medical Press 2017-06-06 /pmc/articles/PMC5473502/ /pubmed/28652745 http://dx.doi.org/10.2147/NDT.S137292 Text en © 2017 Huang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Huang, Suhua Zhou, Fuqing Jiang, Jian Huang, Muhua Zeng, Xianjun Ding, Shan Gong, Honghan Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title | Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title_full | Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title_fullStr | Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title_full_unstemmed | Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title_short | Regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
title_sort | regional impairment of intrinsic functional connectivity strength in patients with chronic primary insomnia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473502/ https://www.ncbi.nlm.nih.gov/pubmed/28652745 http://dx.doi.org/10.2147/NDT.S137292 |
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