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Magnetoencephalographic correlates of mood and reward dynamics in human adolescents
Despite its omnipresence in everyday interactions and its importance for mental health, mood and its neuronal underpinnings are poorly understood. Computational models can help identify parameters affecting self-reported mood during mood induction tasks. Here, we test if computationally modeled dyna...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340400/ https://www.ncbi.nlm.nih.gov/pubmed/34921602 http://dx.doi.org/10.1093/cercor/bhab417 |
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author | Liuzzi, Lucrezia Chang, Katharine K Zheng, Charles Keren, Hanna Saha, Dipta Nielson, Dylan M Stringaris, Argyris |
author_facet | Liuzzi, Lucrezia Chang, Katharine K Zheng, Charles Keren, Hanna Saha, Dipta Nielson, Dylan M Stringaris, Argyris |
author_sort | Liuzzi, Lucrezia |
collection | PubMed |
description | Despite its omnipresence in everyday interactions and its importance for mental health, mood and its neuronal underpinnings are poorly understood. Computational models can help identify parameters affecting self-reported mood during mood induction tasks. Here, we test if computationally modeled dynamics of self-reported mood during monetary gambling can be used to identify trial-by-trial variations in neuronal activity. To this end, we shifted mood in healthy (N = 24) and depressed (N = 30) adolescents by delivering individually tailored reward prediction errors while recording magnetoencephalography (MEG) data. Following a pre-registered analysis, we hypothesize that the expectation component of mood would be predictive of beta-gamma oscillatory power (25–40 Hz). We also hypothesize that trial variations in the source localized responses to reward feedback would be predicted by mood and by its reward prediction error component. Through our multilevel statistical analysis, we found confirmatory evidence that beta-gamma power is positively related to reward expectation during mood shifts, with localized sources in the posterior cingulate cortex. We also confirmed reward prediction error to be predictive of trial-level variations in the response of the paracentral lobule. To our knowledge, this is the first study to harness computational models of mood to relate mood fluctuations to variations in neural oscillations with MEG. |
format | Online Article Text |
id | pubmed-9340400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93404002022-08-01 Magnetoencephalographic correlates of mood and reward dynamics in human adolescents Liuzzi, Lucrezia Chang, Katharine K Zheng, Charles Keren, Hanna Saha, Dipta Nielson, Dylan M Stringaris, Argyris Cereb Cortex Original Article Despite its omnipresence in everyday interactions and its importance for mental health, mood and its neuronal underpinnings are poorly understood. Computational models can help identify parameters affecting self-reported mood during mood induction tasks. Here, we test if computationally modeled dynamics of self-reported mood during monetary gambling can be used to identify trial-by-trial variations in neuronal activity. To this end, we shifted mood in healthy (N = 24) and depressed (N = 30) adolescents by delivering individually tailored reward prediction errors while recording magnetoencephalography (MEG) data. Following a pre-registered analysis, we hypothesize that the expectation component of mood would be predictive of beta-gamma oscillatory power (25–40 Hz). We also hypothesize that trial variations in the source localized responses to reward feedback would be predicted by mood and by its reward prediction error component. Through our multilevel statistical analysis, we found confirmatory evidence that beta-gamma power is positively related to reward expectation during mood shifts, with localized sources in the posterior cingulate cortex. We also confirmed reward prediction error to be predictive of trial-level variations in the response of the paracentral lobule. To our knowledge, this is the first study to harness computational models of mood to relate mood fluctuations to variations in neural oscillations with MEG. Oxford University Press 2021-12-18 /pmc/articles/PMC9340400/ /pubmed/34921602 http://dx.doi.org/10.1093/cercor/bhab417 Text en © The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Liuzzi, Lucrezia Chang, Katharine K Zheng, Charles Keren, Hanna Saha, Dipta Nielson, Dylan M Stringaris, Argyris Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title | Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title_full | Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title_fullStr | Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title_full_unstemmed | Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title_short | Magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
title_sort | magnetoencephalographic correlates of mood and reward dynamics in human adolescents |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340400/ https://www.ncbi.nlm.nih.gov/pubmed/34921602 http://dx.doi.org/10.1093/cercor/bhab417 |
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