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EEG-responses to mood induction interact with seasonality and age
The EEG is suggested as a potential diagnostic and prognostic biomarker for seasonal affective disorder (SAD). As a pre-clinical form of SAD, seasonality is operationalized as seasonal variation in mood, appetite, weight, sleep, energy, and socializing. Importantly, both EEG biomarkers and seasonali...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396338/ https://www.ncbi.nlm.nih.gov/pubmed/36016970 http://dx.doi.org/10.3389/fpsyt.2022.950328 |
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author | Höller, Yvonne Jónsdóttir, Sara Teresa Hannesdóttir, Anna Hjálmveig Ólafsson, Ragnar Pétur |
author_facet | Höller, Yvonne Jónsdóttir, Sara Teresa Hannesdóttir, Anna Hjálmveig Ólafsson, Ragnar Pétur |
author_sort | Höller, Yvonne |
collection | PubMed |
description | The EEG is suggested as a potential diagnostic and prognostic biomarker for seasonal affective disorder (SAD). As a pre-clinical form of SAD, seasonality is operationalized as seasonal variation in mood, appetite, weight, sleep, energy, and socializing. Importantly, both EEG biomarkers and seasonality interact with age. Inducing sad mood to assess cognitive vulnerability was suggested to improve the predictive value of summer assessments for winter depression. However, no EEG studies have been conducted on induced sad mood in relation to seasonality, and no studies so far have controlled for age. We recorded EEG and calculated bandpower in 114 participants during rest and during induced sad mood in summer. Participants were grouped by age and based on a seasonality score as obtained with the seasonal pattern assessment questionnaire (SPAQ). Participants with high seasonality scores showed significantly larger changes in EEG power from rest to sad mood induction, specifically in the alpha frequency range (p = 0.027), compared to participants with low seasonality scores. Furthermore, seasonality interacted significantly with age (p < 0.001), with lower activity in individuals with high seasonality scores that were older than 50 years but the opposite pattern in individuals up to 50 years. Effects of sad mood induction on brain activity are related to seasonality and can therefore be consider as potential predicting biomarkers for SAD. Future studies should control for age as a confounding factor, and more studies are needed to elaborate on the characteristics of EEG biomarkers in participants above 50 years. |
format | Online Article Text |
id | pubmed-9396338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93963382022-08-24 EEG-responses to mood induction interact with seasonality and age Höller, Yvonne Jónsdóttir, Sara Teresa Hannesdóttir, Anna Hjálmveig Ólafsson, Ragnar Pétur Front Psychiatry Psychiatry The EEG is suggested as a potential diagnostic and prognostic biomarker for seasonal affective disorder (SAD). As a pre-clinical form of SAD, seasonality is operationalized as seasonal variation in mood, appetite, weight, sleep, energy, and socializing. Importantly, both EEG biomarkers and seasonality interact with age. Inducing sad mood to assess cognitive vulnerability was suggested to improve the predictive value of summer assessments for winter depression. However, no EEG studies have been conducted on induced sad mood in relation to seasonality, and no studies so far have controlled for age. We recorded EEG and calculated bandpower in 114 participants during rest and during induced sad mood in summer. Participants were grouped by age and based on a seasonality score as obtained with the seasonal pattern assessment questionnaire (SPAQ). Participants with high seasonality scores showed significantly larger changes in EEG power from rest to sad mood induction, specifically in the alpha frequency range (p = 0.027), compared to participants with low seasonality scores. Furthermore, seasonality interacted significantly with age (p < 0.001), with lower activity in individuals with high seasonality scores that were older than 50 years but the opposite pattern in individuals up to 50 years. Effects of sad mood induction on brain activity are related to seasonality and can therefore be consider as potential predicting biomarkers for SAD. Future studies should control for age as a confounding factor, and more studies are needed to elaborate on the characteristics of EEG biomarkers in participants above 50 years. Frontiers Media S.A. 2022-08-09 /pmc/articles/PMC9396338/ /pubmed/36016970 http://dx.doi.org/10.3389/fpsyt.2022.950328 Text en Copyright © 2022 Höller, Jónsdóttir, Hannesdóttir and Ólafsson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Höller, Yvonne Jónsdóttir, Sara Teresa Hannesdóttir, Anna Hjálmveig Ólafsson, Ragnar Pétur EEG-responses to mood induction interact with seasonality and age |
title | EEG-responses to mood induction interact with seasonality and age |
title_full | EEG-responses to mood induction interact with seasonality and age |
title_fullStr | EEG-responses to mood induction interact with seasonality and age |
title_full_unstemmed | EEG-responses to mood induction interact with seasonality and age |
title_short | EEG-responses to mood induction interact with seasonality and age |
title_sort | eeg-responses to mood induction interact with seasonality and age |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396338/ https://www.ncbi.nlm.nih.gov/pubmed/36016970 http://dx.doi.org/10.3389/fpsyt.2022.950328 |
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