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Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence
Although blunted sensitivity to reward is thought to play a key role in promoting risk for depression, most research on this topic has utilized monetary reward paradigms and focused on currently depressed adults. To address this issue, we analyzed neural reward and β-endorphin data from the Psychobi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287766/ https://www.ncbi.nlm.nih.gov/pubmed/35856064 http://dx.doi.org/10.1016/j.cpnec.2022.100149 |
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author | Gray, Zach J. Shields, Grant S. Sichko, Stassja Bui, Theresa Q. Vinograd, Meghan Olvera-Alvarez, Hector A. Slavich, George M. |
author_facet | Gray, Zach J. Shields, Grant S. Sichko, Stassja Bui, Theresa Q. Vinograd, Meghan Olvera-Alvarez, Hector A. Slavich, George M. |
author_sort | Gray, Zach J. |
collection | PubMed |
description | Although blunted sensitivity to reward is thought to play a key role in promoting risk for depression, most research on this topic has utilized monetary reward paradigms and focused on currently depressed adults. To address this issue, we analyzed neural reward and β-endorphin data from the Psychobiology of Stress and Adolescent Depression (PSY SAD) Study, which recruited a well-characterized sample of adolescent girls at high vs. low risk for major depressive disorder (MDD) (N = 52, M(age) = 14.90, SD = 1.35) based on their mothers’ lifetime history of MDD. As hypothesized, greater striatal activity while receiving positive (vs. neutral) social evaluation was associated with lower depression symptom severity as independently assessed by the Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS). This association was present for girls at high but not low risk for MDD, suggesting that this neural response may represent a pre-clinical marker of risk for depression. Consistent with these results, higher post-social evaluation levels of a peripheral marker of reward sensitivity, β-endorphin, were related to lower clinician-rated depression symptom severity. Together, these results indicate that neural and peripheral markers of responsivity to social reward are both related to depression severity, which may have implications for understanding the pathophysiology of depression. |
format | Online Article Text |
id | pubmed-9287766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92877662022-07-17 Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence Gray, Zach J. Shields, Grant S. Sichko, Stassja Bui, Theresa Q. Vinograd, Meghan Olvera-Alvarez, Hector A. Slavich, George M. Compr Psychoneuroendocrinol Article Although blunted sensitivity to reward is thought to play a key role in promoting risk for depression, most research on this topic has utilized monetary reward paradigms and focused on currently depressed adults. To address this issue, we analyzed neural reward and β-endorphin data from the Psychobiology of Stress and Adolescent Depression (PSY SAD) Study, which recruited a well-characterized sample of adolescent girls at high vs. low risk for major depressive disorder (MDD) (N = 52, M(age) = 14.90, SD = 1.35) based on their mothers’ lifetime history of MDD. As hypothesized, greater striatal activity while receiving positive (vs. neutral) social evaluation was associated with lower depression symptom severity as independently assessed by the Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS). This association was present for girls at high but not low risk for MDD, suggesting that this neural response may represent a pre-clinical marker of risk for depression. Consistent with these results, higher post-social evaluation levels of a peripheral marker of reward sensitivity, β-endorphin, were related to lower clinician-rated depression symptom severity. Together, these results indicate that neural and peripheral markers of responsivity to social reward are both related to depression severity, which may have implications for understanding the pathophysiology of depression. Elsevier 2022-06-16 /pmc/articles/PMC9287766/ /pubmed/35856064 http://dx.doi.org/10.1016/j.cpnec.2022.100149 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Gray, Zach J. Shields, Grant S. Sichko, Stassja Bui, Theresa Q. Vinograd, Meghan Olvera-Alvarez, Hector A. Slavich, George M. Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title | Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title_full | Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title_fullStr | Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title_full_unstemmed | Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title_short | Neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
title_sort | neural and peripheral markers of reward during positive social evaluation are associated with less clinician-rated depression symptom severity in adolescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287766/ https://www.ncbi.nlm.nih.gov/pubmed/35856064 http://dx.doi.org/10.1016/j.cpnec.2022.100149 |
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