Intra brainstem connectivity is impaired in chronic fatigue syndrome.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2019
Historique:
received: 07 05 2019
revised: 27 08 2019
accepted: 17 10 2019
pubmed: 2 11 2019
medline: 23 9 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31671321
pii: S2213-1582(19)30392-4
doi: 10.1016/j.nicl.2019.102045
pmc: PMC6835065
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102045

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Leighton R Barnden (LR)

National Centre for Neuroimmunology and Emerging Diseases, Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia. Electronic address: l.barnden@griffith.edu.au.

Zack Y Shan (ZY)

National Centre for Neuroimmunology and Emerging Diseases, Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Sunshine Coast Mind and Neuroscience Thompson Institute, University of the Sunshine Coast, Birtinya, QLD 4575, Australia. Electronic address: zhan@usc.edu.au.

Donald R Staines (DR)

National Centre for Neuroimmunology and Emerging Diseases, Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia. Electronic address: d.staines@griffith.edu.au.

Sonya Marshall-Gradisnik (S)

National Centre for Neuroimmunology and Emerging Diseases, Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia. Electronic address: s.marshall-gradisnik@griffith.edu.au.

Kevin Finegan (K)

Medical Imaging Department, Gold Coast University Hospital, Parklands, QLD 4215, Australia. Electronic address: Finegan@health.qld.gov.au.

Timothy Ireland (T)

Medical Imaging Department, Gold Coast University Hospital, Parklands, QLD 4215, Australia. Electronic address: Ireland@health.qld.gov.au.

Sandeep Bhuta (S)

Medical Imaging Department, Gold Coast University Hospital, Parklands, QLD 4215, Australia.

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