Altered Brain Microstate Dynamics in Adolescents with Narcolepsy

Narcolepsy is a chronic sleep disorder caused by a loss of hypocretin-1 producing neurons in the hypothalamus. Previous neuroimaging studies have investigated brain function in narcolepsy during rest using positron emission tomography (PET) and single photon emission computed tomography (SPECT). In...

Full description

Bibliographic Details
Main Authors: Natasha M. Drissi, Attila Szakács, Suzanne T. Witt, Anna Wretman, Martin Ulander, Henriettae Ståhlbrandt, Niklas Darin, Tove Hallböök, Anne-Marie Landtblom, Maria Engström
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnhum.2016.00369/full
id doaj-f141ec35999d430681d4b872ff678f3d
record_format Article
spelling doaj-f141ec35999d430681d4b872ff678f3d2020-11-25T03:32:05ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612016-08-011010.3389/fnhum.2016.00369186894Altered Brain Microstate Dynamics in Adolescents with NarcolepsyNatasha M. Drissi0Natasha M. Drissi1Attila Szakács2Suzanne T. Witt3Anna Wretman4Martin Ulander5Henriettae Ståhlbrandt6Niklas Darin7Tove Hallböök8Anne-Marie Landtblom9Anne-Marie Landtblom10Maria Engström11Maria Engström12Department of Medical and Health Sciences (IMH), Linköping UniversityLinköping, SwedenCenter for Medical Image Science and Visualization (CMIV), Linköping UniversityLinköping, SwedenDepartment of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of GothenburgGothenburg, SwedenCenter for Medical Image Science and Visualization (CMIV), Linköping UniversityLinköping, SwedenDepartment of Behavioral Science and Learning, Linköping UniversityLinköping, SwedenDepartment of Clinical and Experimental Medicine, Linköping UniversityLinköping, SwedenDepartment of Radiology, Medical Diagnostics, Highland HospitalEksjö, SwedenDepartment of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of GothenburgGothenburg, SwedenDepartment of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of GothenburgGothenburg, SwedenDepartment of Clinical and Experimental Medicine, Linköping UniversityLinköping, SwedenDepartment of Neurology, Uppsala UniversityUppsala, SwedenDepartment of Medical and Health Sciences (IMH), Linköping UniversityLinköping, SwedenCenter for Medical Image Science and Visualization (CMIV), Linköping UniversityLinköping, SwedenNarcolepsy is a chronic sleep disorder caused by a loss of hypocretin-1 producing neurons in the hypothalamus. Previous neuroimaging studies have investigated brain function in narcolepsy during rest using positron emission tomography (PET) and single photon emission computed tomography (SPECT). In addition to hypothalamic and thalamic dysfunction they showed aberrant prefrontal perfusion and glucose metabolism in narcolepsy. Given these findings in brain structure and metabolism in narcolepsy, we anticipated that changes in functional magnetic resonance imaging (fMRI) resting state network (RSN) dynamics might also be apparent in patients with narcolepsy. The objective of this study was to investigate and describe brain microstate activity in adolescents with narcolepsy and correlate these to RSNs using simultaneous fMRI and electroencephalography (EEG). Sixteen adolescents (ages 13–20) with a confirmed diagnosis of narcolepsy were recruited and compared to age-matched healthy controls. Simultaneous EEG and fMRI data were collected during 10 min of wakeful rest. EEG data were analyzed for microstates, which are discrete epochs of stable global brain states obtained from topographical EEG analysis. Functional MRI data were analyzed for RSNs. Data showed that narcolepsy patients were less likely than controls to spend time in a microstate which we found to be related to the default mode network and may suggest a disruption of this network that is disease specific. We concluded that adolescents with narcolepsy have altered resting state brain dynamics.https://www.frontiersin.org/article/10.3389/fnhum.2016.00369/fullnarcolepsydefault mode networkfunctional magnetic resonance imaging (fMRI)electroencephalography (EEG)microstatesresting state networks
collection DOAJ
language English
format Article
sources DOAJ
author Natasha M. Drissi
Natasha M. Drissi
Attila Szakács
Suzanne T. Witt
Anna Wretman
Martin Ulander
Henriettae Ståhlbrandt
Niklas Darin
Tove Hallböök
Anne-Marie Landtblom
Anne-Marie Landtblom
Maria Engström
Maria Engström
spellingShingle Natasha M. Drissi
Natasha M. Drissi
Attila Szakács
Suzanne T. Witt
Anna Wretman
Martin Ulander
Henriettae Ståhlbrandt
Niklas Darin
Tove Hallböök
Anne-Marie Landtblom
Anne-Marie Landtblom
Maria Engström
Maria Engström
Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
Frontiers in Human Neuroscience
narcolepsy
default mode network
functional magnetic resonance imaging (fMRI)
electroencephalography (EEG)
microstates
resting state networks
author_facet Natasha M. Drissi
Natasha M. Drissi
Attila Szakács
Suzanne T. Witt
Anna Wretman
Martin Ulander
Henriettae Ståhlbrandt
Niklas Darin
Tove Hallböök
Anne-Marie Landtblom
Anne-Marie Landtblom
Maria Engström
Maria Engström
author_sort Natasha M. Drissi
title Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
title_short Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
title_full Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
title_fullStr Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
title_full_unstemmed Altered Brain Microstate Dynamics in Adolescents with Narcolepsy
title_sort altered brain microstate dynamics in adolescents with narcolepsy
publisher Frontiers Media S.A.
series Frontiers in Human Neuroscience
issn 1662-5161
publishDate 2016-08-01
description Narcolepsy is a chronic sleep disorder caused by a loss of hypocretin-1 producing neurons in the hypothalamus. Previous neuroimaging studies have investigated brain function in narcolepsy during rest using positron emission tomography (PET) and single photon emission computed tomography (SPECT). In addition to hypothalamic and thalamic dysfunction they showed aberrant prefrontal perfusion and glucose metabolism in narcolepsy. Given these findings in brain structure and metabolism in narcolepsy, we anticipated that changes in functional magnetic resonance imaging (fMRI) resting state network (RSN) dynamics might also be apparent in patients with narcolepsy. The objective of this study was to investigate and describe brain microstate activity in adolescents with narcolepsy and correlate these to RSNs using simultaneous fMRI and electroencephalography (EEG). Sixteen adolescents (ages 13–20) with a confirmed diagnosis of narcolepsy were recruited and compared to age-matched healthy controls. Simultaneous EEG and fMRI data were collected during 10 min of wakeful rest. EEG data were analyzed for microstates, which are discrete epochs of stable global brain states obtained from topographical EEG analysis. Functional MRI data were analyzed for RSNs. Data showed that narcolepsy patients were less likely than controls to spend time in a microstate which we found to be related to the default mode network and may suggest a disruption of this network that is disease specific. We concluded that adolescents with narcolepsy have altered resting state brain dynamics.
topic narcolepsy
default mode network
functional magnetic resonance imaging (fMRI)
electroencephalography (EEG)
microstates
resting state networks
url https://www.frontiersin.org/article/10.3389/fnhum.2016.00369/full
work_keys_str_mv AT natashamdrissi alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT natashamdrissi alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT attilaszakacs alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT suzannetwitt alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT annawretman alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT martinulander alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT henriettaestahlbrandt alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT niklasdarin alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT tovehallbook alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT annemarielandtblom alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT annemarielandtblom alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT mariaengstrom alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
AT mariaengstrom alteredbrainmicrostatedynamicsinadolescentswithnarcolepsy
_version_ 1724569768016478208