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Intra brainstem connectivity is impaired in chronic fatigue syndrome
In myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS), abnormal MRI correlations with symptom severity and autonomic measures have suggested impaired nerve signal conduction within the brainstem. Here we analyse fMRI correlations to directly test connectivity within and from the brainste...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835065/ https://www.ncbi.nlm.nih.gov/pubmed/31671321 http://dx.doi.org/10.1016/j.nicl.2019.102045 |
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author | Barnden, Leighton R Shan, Zack Y Staines, Donald R Marshall-Gradisnik, Sonya Finegan, Kevin Ireland, Timothy Bhuta, Sandeep |
author_facet | Barnden, Leighton R Shan, Zack Y Staines, Donald R Marshall-Gradisnik, Sonya Finegan, Kevin Ireland, Timothy Bhuta, Sandeep |
author_sort | Barnden, Leighton R |
collection | PubMed |
description | In myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS), abnormal MRI correlations with symptom severity and autonomic measures have suggested impaired nerve signal conduction within the brainstem. Here we analyse fMRI correlations to directly test connectivity within and from the brainstem. Resting and task functional MRI (fMRI) were acquired for 45 ME/CFS (Fukuda criteria) and 27 healthy controls (HC). We selected limited brainstem reticular activation system (RAS) regions-of-interest (ROIs) based on previous structural MRI findings in a different ME/CFS cohort (bilateral rostral medulla and midbrain cuneiform nucleus), the dorsal Raphe nucleus, and two subcortical ROIs (hippocampus subiculum and thalamus intralaminar nucleus) reported to have rich brainstem connections. When HC and ME/CFS were analysed separately, significant correlations were detected for both groups during both rest and task, with stronger correlations during task than rest. In ME/CFS, connections were absent between medulla and midbrain nuclei, although hippocampal connections with these nuclei were enhanced. When corresponding correlations from HC and ME/CFS were compared, ME/CFS connectivity deficits were detected within the brainstem between the medulla and cuneiform nucleus and between the brainstem and hippocampus and intralaminar thalamus, but only during task. In CFS/ME, weaker connectivity between some RAS nuclei was associated with increased symptom severity. RAS neuron oscillatory signals facilitate coherence in thalamo-cortical oscillations. Brainstem RAS connectivity deficits can explain autonomic changes and diminish cortical oscillatory coherence which can impair attention, memory, cognitive function, sleep quality and muscle tone, all symptoms of ME/CFS. |
format | Online Article Text |
id | pubmed-6835065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68350652019-11-12 Intra brainstem connectivity is impaired in chronic fatigue syndrome Barnden, Leighton R Shan, Zack Y Staines, Donald R Marshall-Gradisnik, Sonya Finegan, Kevin Ireland, Timothy Bhuta, Sandeep Neuroimage Clin Regular Article In myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS), abnormal MRI correlations with symptom severity and autonomic measures have suggested impaired nerve signal conduction within the brainstem. Here we analyse fMRI correlations to directly test connectivity within and from the brainstem. Resting and task functional MRI (fMRI) were acquired for 45 ME/CFS (Fukuda criteria) and 27 healthy controls (HC). We selected limited brainstem reticular activation system (RAS) regions-of-interest (ROIs) based on previous structural MRI findings in a different ME/CFS cohort (bilateral rostral medulla and midbrain cuneiform nucleus), the dorsal Raphe nucleus, and two subcortical ROIs (hippocampus subiculum and thalamus intralaminar nucleus) reported to have rich brainstem connections. When HC and ME/CFS were analysed separately, significant correlations were detected for both groups during both rest and task, with stronger correlations during task than rest. In ME/CFS, connections were absent between medulla and midbrain nuclei, although hippocampal connections with these nuclei were enhanced. When corresponding correlations from HC and ME/CFS were compared, ME/CFS connectivity deficits were detected within the brainstem between the medulla and cuneiform nucleus and between the brainstem and hippocampus and intralaminar thalamus, but only during task. In CFS/ME, weaker connectivity between some RAS nuclei was associated with increased symptom severity. RAS neuron oscillatory signals facilitate coherence in thalamo-cortical oscillations. Brainstem RAS connectivity deficits can explain autonomic changes and diminish cortical oscillatory coherence which can impair attention, memory, cognitive function, sleep quality and muscle tone, all symptoms of ME/CFS. Elsevier 2019-10-19 /pmc/articles/PMC6835065/ /pubmed/31671321 http://dx.doi.org/10.1016/j.nicl.2019.102045 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Barnden, Leighton R Shan, Zack Y Staines, Donald R Marshall-Gradisnik, Sonya Finegan, Kevin Ireland, Timothy Bhuta, Sandeep Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title | Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title_full | Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title_fullStr | Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title_full_unstemmed | Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title_short | Intra brainstem connectivity is impaired in chronic fatigue syndrome |
title_sort | intra brainstem connectivity is impaired in chronic fatigue syndrome |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835065/ https://www.ncbi.nlm.nih.gov/pubmed/31671321 http://dx.doi.org/10.1016/j.nicl.2019.102045 |
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