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How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence
INTRODUCTION: Understanding the emotional responsivity style and neurocognitive profiles of depression‐related processes in at‐risk youth may be helpful in revealing those most likely to develop affective disorders. However, the multiplicity of biopsychosocial risk factors makes it difficult to dise...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119860/ https://www.ncbi.nlm.nih.gov/pubmed/33662187 http://dx.doi.org/10.1002/brb3.2005 |
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author | Stretton, Jason Walsh, Nicholas D Mobbs, Dean Schweizer, Susanne van Harmelen, Anne‐Laura Lombardo, Michael Goodyer, Ian Dalgleish, Tim |
author_facet | Stretton, Jason Walsh, Nicholas D Mobbs, Dean Schweizer, Susanne van Harmelen, Anne‐Laura Lombardo, Michael Goodyer, Ian Dalgleish, Tim |
author_sort | Stretton, Jason |
collection | PubMed |
description | INTRODUCTION: Understanding the emotional responsivity style and neurocognitive profiles of depression‐related processes in at‐risk youth may be helpful in revealing those most likely to develop affective disorders. However, the multiplicity of biopsychosocial risk factors makes it difficult to disentangle unique and combined effects at a neurobiological level. METHODS: In a population‐derived sample of 56 older adolescents (aged 17–20), we adopted partial least squares regression and correlation models to explore the relationships between multivariate biopsychosocial risks for later depression, emotional response style, and fMRI activity, to rejecting and inclusive social feedback. RESULTS: Behaviorally, higher depressive risk was associated with both reduced negative affect following negative social feedback and reduced positive affect following positive social feedback. In response to both cues of rejection and inclusion, we observed a general neural pattern of increased cingulate, temporal, and striatal activity in the brain. Secondly, in response to rejection only, we observed a pattern of activity in ostensibly executive control‐ and emotion regulation‐related brain regions encompassing fronto‐parietal brain networks including the angular gyrus. CONCLUSION: The results suggest that risk for depression is associated with a pervasive emotional insensitivity in the face of positive and negative social feedback. |
format | Online Article Text |
id | pubmed-8119860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81198602021-05-20 How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence Stretton, Jason Walsh, Nicholas D Mobbs, Dean Schweizer, Susanne van Harmelen, Anne‐Laura Lombardo, Michael Goodyer, Ian Dalgleish, Tim Brain Behav Original Research INTRODUCTION: Understanding the emotional responsivity style and neurocognitive profiles of depression‐related processes in at‐risk youth may be helpful in revealing those most likely to develop affective disorders. However, the multiplicity of biopsychosocial risk factors makes it difficult to disentangle unique and combined effects at a neurobiological level. METHODS: In a population‐derived sample of 56 older adolescents (aged 17–20), we adopted partial least squares regression and correlation models to explore the relationships between multivariate biopsychosocial risks for later depression, emotional response style, and fMRI activity, to rejecting and inclusive social feedback. RESULTS: Behaviorally, higher depressive risk was associated with both reduced negative affect following negative social feedback and reduced positive affect following positive social feedback. In response to both cues of rejection and inclusion, we observed a general neural pattern of increased cingulate, temporal, and striatal activity in the brain. Secondly, in response to rejection only, we observed a pattern of activity in ostensibly executive control‐ and emotion regulation‐related brain regions encompassing fronto‐parietal brain networks including the angular gyrus. CONCLUSION: The results suggest that risk for depression is associated with a pervasive emotional insensitivity in the face of positive and negative social feedback. John Wiley and Sons Inc. 2021-03-04 /pmc/articles/PMC8119860/ /pubmed/33662187 http://dx.doi.org/10.1002/brb3.2005 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Stretton, Jason Walsh, Nicholas D Mobbs, Dean Schweizer, Susanne van Harmelen, Anne‐Laura Lombardo, Michael Goodyer, Ian Dalgleish, Tim How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title | How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title_full | How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title_fullStr | How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title_full_unstemmed | How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title_short | How biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
title_sort | how biopsychosocial depressive risk shapes behavioral and neural responses to social evaluation in adolescence |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119860/ https://www.ncbi.nlm.nih.gov/pubmed/33662187 http://dx.doi.org/10.1002/brb3.2005 |
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