Cargando…

Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome

Impairments in cognition, pain intolerance, and physical inactivity characterize adolescent chronic fatigue syndrome (CFS), yet little is known about its neurobiology. The right dorsal anterior insular (dAI) connectivity of the salience network provides a motivational context to stimuli. In this stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Wortinger, Laura Anne, Glenne Øie, Merete, Endestad, Tor, Bruun Wyller, Vegard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589232/
https://www.ncbi.nlm.nih.gov/pubmed/28880891
http://dx.doi.org/10.1371/journal.pone.0184325
_version_ 1783262294143139840
author Wortinger, Laura Anne
Glenne Øie, Merete
Endestad, Tor
Bruun Wyller, Vegard
author_facet Wortinger, Laura Anne
Glenne Øie, Merete
Endestad, Tor
Bruun Wyller, Vegard
author_sort Wortinger, Laura Anne
collection PubMed
description Impairments in cognition, pain intolerance, and physical inactivity characterize adolescent chronic fatigue syndrome (CFS), yet little is known about its neurobiology. The right dorsal anterior insular (dAI) connectivity of the salience network provides a motivational context to stimuli. In this study, we examined regional functional connectivity (FC) patterns of the right dAI in adolescent CFS patients and healthy participants. Eighteen adolescent patients with CFS and 18 aged-matched healthy adolescent control participants underwent resting-state functional magnetic resonance imaging. The right dAI region of interest was examined in a seed-to-voxel resting-state FC analysis using SPM and CONN toolbox. Relative to healthy adolescents, CFS patients demonstrated reduced FC of the right dAI to the right posterior parietal cortex (PPC) node of the central executive network. The decreased FC of the right dAI–PPC might indicate impaired cognitive control development in adolescent CFS. Immature FC of the right dAI–PPC in patients also lacked associations with three known functional domains: cognition, pain and physical activity, which were observed in the healthy group. These results suggest a distinct biological signature of adolescent CFS and might represent a fundamental role of the dAI in motivated behavior.
format Online
Article
Text
id pubmed-5589232
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-55892322017-09-15 Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome Wortinger, Laura Anne Glenne Øie, Merete Endestad, Tor Bruun Wyller, Vegard PLoS One Research Article Impairments in cognition, pain intolerance, and physical inactivity characterize adolescent chronic fatigue syndrome (CFS), yet little is known about its neurobiology. The right dorsal anterior insular (dAI) connectivity of the salience network provides a motivational context to stimuli. In this study, we examined regional functional connectivity (FC) patterns of the right dAI in adolescent CFS patients and healthy participants. Eighteen adolescent patients with CFS and 18 aged-matched healthy adolescent control participants underwent resting-state functional magnetic resonance imaging. The right dAI region of interest was examined in a seed-to-voxel resting-state FC analysis using SPM and CONN toolbox. Relative to healthy adolescents, CFS patients demonstrated reduced FC of the right dAI to the right posterior parietal cortex (PPC) node of the central executive network. The decreased FC of the right dAI–PPC might indicate impaired cognitive control development in adolescent CFS. Immature FC of the right dAI–PPC in patients also lacked associations with three known functional domains: cognition, pain and physical activity, which were observed in the healthy group. These results suggest a distinct biological signature of adolescent CFS and might represent a fundamental role of the dAI in motivated behavior. Public Library of Science 2017-09-07 /pmc/articles/PMC5589232/ /pubmed/28880891 http://dx.doi.org/10.1371/journal.pone.0184325 Text en © 2017 Wortinger et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wortinger, Laura Anne
Glenne Øie, Merete
Endestad, Tor
Bruun Wyller, Vegard
Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title_full Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title_fullStr Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title_full_unstemmed Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title_short Altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
title_sort altered right anterior insular connectivity and loss of associated functions in adolescent chronic fatigue syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589232/
https://www.ncbi.nlm.nih.gov/pubmed/28880891
http://dx.doi.org/10.1371/journal.pone.0184325
work_keys_str_mv AT wortingerlauraanne alteredrightanteriorinsularconnectivityandlossofassociatedfunctionsinadolescentchronicfatiguesyndrome
AT glenneøiemerete alteredrightanteriorinsularconnectivityandlossofassociatedfunctionsinadolescentchronicfatiguesyndrome
AT endestadtor alteredrightanteriorinsularconnectivityandlossofassociatedfunctionsinadolescentchronicfatiguesyndrome
AT bruunwyllervegard alteredrightanteriorinsularconnectivityandlossofassociatedfunctionsinadolescentchronicfatiguesyndrome