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Cerebral Asymmetry in Insomnia Sufferers

Cerebral asymmetry is used to describe the differences in electroencephalographic activity between regions of the brain. The objective of this study was to document frontal, central, and parietal asymmetry in psychophysiological (Psy-I) and paradoxical (Para-I) insomnia sufferers as well as good sle...

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Autores principales: St-Jean, Geneviève, Turcotte, Isabelle, Bastien, Célyne H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315843/
https://www.ncbi.nlm.nih.gov/pubmed/22479257
http://dx.doi.org/10.3389/fneur.2012.00047
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author St-Jean, Geneviève
Turcotte, Isabelle
Bastien, Célyne H.
author_facet St-Jean, Geneviève
Turcotte, Isabelle
Bastien, Célyne H.
author_sort St-Jean, Geneviève
collection PubMed
description Cerebral asymmetry is used to describe the differences in electroencephalographic activity between regions of the brain. The objective of this study was to document frontal, central, and parietal asymmetry in psychophysiological (Psy-I) and paradoxical (Para-I) insomnia sufferers as well as good sleeper (GS) controls, and to compare their patterns of asymmetry to others already found in anxiety and depression. Additionally, asymmetry variations between nights were assessed. Participants were 17 Psy-I, 14 Para-I, and 19 GS (mean age = 40 years, SD = 9.4). They completed three nights of polysomnography (PSG) recordings following a clinical evaluation in a sleep laboratory. All sleep cycles of Nights 2 and 3 were retained for power spectral analysis. The absolute activity in frequency bands (0.00–125.00 Hz) was computed at multiple frontal, central, and parietal sites in rapid eye movement and non-rapid eye movement sleep to provide cerebral asymmetry measures. Mixed model ANOVAs were computed to assess differences between groups and nights. Correlations were performed with asymmetry and symptoms of depression and anxiety from self-reported questionnaires. Over the course of the two nights, Para-I tended to present hypoactivation of their left frontal region but hyperactivation of their right one compared with GS. As for Psy-I, they presented increased activation of their right parietal region compared with Para-I. Asymmetry at frontal, central, and parietal region differed between nights. On a more disrupted night of sleep, Psy-I had increased activity in their right parietal region while Para-I presented a decrease in cerebral activity in the right central region on their less disrupted night of sleep. Anxious and depressive symptoms did not correlate with asymmetry at any region. Therefore, Psy-I and Para-I present unique patterns of cerebral asymmetry that do not relate to depression or anxiety, and asymmetry varies between nights, maybe as a consequence of variability in objective sleep quality from night to night.
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spelling pubmed-33158432012-04-04 Cerebral Asymmetry in Insomnia Sufferers St-Jean, Geneviève Turcotte, Isabelle Bastien, Célyne H. Front Neurol Neuroscience Cerebral asymmetry is used to describe the differences in electroencephalographic activity between regions of the brain. The objective of this study was to document frontal, central, and parietal asymmetry in psychophysiological (Psy-I) and paradoxical (Para-I) insomnia sufferers as well as good sleeper (GS) controls, and to compare their patterns of asymmetry to others already found in anxiety and depression. Additionally, asymmetry variations between nights were assessed. Participants were 17 Psy-I, 14 Para-I, and 19 GS (mean age = 40 years, SD = 9.4). They completed three nights of polysomnography (PSG) recordings following a clinical evaluation in a sleep laboratory. All sleep cycles of Nights 2 and 3 were retained for power spectral analysis. The absolute activity in frequency bands (0.00–125.00 Hz) was computed at multiple frontal, central, and parietal sites in rapid eye movement and non-rapid eye movement sleep to provide cerebral asymmetry measures. Mixed model ANOVAs were computed to assess differences between groups and nights. Correlations were performed with asymmetry and symptoms of depression and anxiety from self-reported questionnaires. Over the course of the two nights, Para-I tended to present hypoactivation of their left frontal region but hyperactivation of their right one compared with GS. As for Psy-I, they presented increased activation of their right parietal region compared with Para-I. Asymmetry at frontal, central, and parietal region differed between nights. On a more disrupted night of sleep, Psy-I had increased activity in their right parietal region while Para-I presented a decrease in cerebral activity in the right central region on their less disrupted night of sleep. Anxious and depressive symptoms did not correlate with asymmetry at any region. Therefore, Psy-I and Para-I present unique patterns of cerebral asymmetry that do not relate to depression or anxiety, and asymmetry varies between nights, maybe as a consequence of variability in objective sleep quality from night to night. Frontiers Research Foundation 2012-03-30 /pmc/articles/PMC3315843/ /pubmed/22479257 http://dx.doi.org/10.3389/fneur.2012.00047 Text en Copyright © 2012 St-Jean, Turcotte and Bastien. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
St-Jean, Geneviève
Turcotte, Isabelle
Bastien, Célyne H.
Cerebral Asymmetry in Insomnia Sufferers
title Cerebral Asymmetry in Insomnia Sufferers
title_full Cerebral Asymmetry in Insomnia Sufferers
title_fullStr Cerebral Asymmetry in Insomnia Sufferers
title_full_unstemmed Cerebral Asymmetry in Insomnia Sufferers
title_short Cerebral Asymmetry in Insomnia Sufferers
title_sort cerebral asymmetry in insomnia sufferers
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315843/
https://www.ncbi.nlm.nih.gov/pubmed/22479257
http://dx.doi.org/10.3389/fneur.2012.00047
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