Cargando…

Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia

Dimensional models of anxiety and depression highlight common and distinct symptom clusters that are thought to reflect disruptions in underlying functional processes. The current study investigated how functioning of threat neurocircuitry relates to symptom dimensions of anxiety and depression. Par...

Descripción completa

Detalles Bibliográficos
Autores principales: Young, Katherine S., Bookheimer, Susan Y., Nusslock, Robin, Zinbarg, Richard E., Damme, Katherine S. F., Chat, Iris Ka-Yi, Kelley, Nicholas J., Vinograd, Meghan, Perez, Marcelina, Chen, Kelly, Cohen, Aileen Echiverri, Craske, Michelle G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280223/
https://www.ncbi.nlm.nih.gov/pubmed/33833400
http://dx.doi.org/10.1038/s41386-021-01003-8
_version_ 1783722607678324736
author Young, Katherine S.
Bookheimer, Susan Y.
Nusslock, Robin
Zinbarg, Richard E.
Damme, Katherine S. F.
Chat, Iris Ka-Yi
Kelley, Nicholas J.
Vinograd, Meghan
Perez, Marcelina
Chen, Kelly
Cohen, Aileen Echiverri
Craske, Michelle G.
author_facet Young, Katherine S.
Bookheimer, Susan Y.
Nusslock, Robin
Zinbarg, Richard E.
Damme, Katherine S. F.
Chat, Iris Ka-Yi
Kelley, Nicholas J.
Vinograd, Meghan
Perez, Marcelina
Chen, Kelly
Cohen, Aileen Echiverri
Craske, Michelle G.
author_sort Young, Katherine S.
collection PubMed
description Dimensional models of anxiety and depression highlight common and distinct symptom clusters that are thought to reflect disruptions in underlying functional processes. The current study investigated how functioning of threat neurocircuitry relates to symptom dimensions of anxiety and depression. Participants were aged 18–19 years (n = 229, 158 female) and were selected to ensure a range of scores on symptom measures. Symptom dimensions of “General Distress” (common to anxiety disorders and depression), “Fears” (more specific to anxiety disorders), and “Anhedonia-apprehension” (more specific to depression) were evaluated. Participants underwent functional magnetic resonance imaging during a Pavlovian fear conditioning paradigm. Multilevel modeling analyses estimated relationships between symptom dimensions and activation in threat neural circuitry. Exploratory whole brain analyses were also conducted. Threat-related neural activity was not associated with General Distress or Fears. Anhedonia-apprehension was associated with activation of bilateral amygdala, anterior insula and dACC during late extinction. We found no evidence to support an association between symptom dimensions of General Distress or Fears with threat circuitry activation in a large sample of young adults. We did, however, find that the symptom dimension of Anhedonia-apprehension was significantly associated with threat-related neural activation during fear extinction. This effect requires replication in future work but may reflect anhedonic impairments in learning when contingencies are altered, possibly linked to the rewarding relief of an unexpectedly absent threat.
format Online
Article
Text
id pubmed-8280223
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-82802232021-07-23 Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia Young, Katherine S. Bookheimer, Susan Y. Nusslock, Robin Zinbarg, Richard E. Damme, Katherine S. F. Chat, Iris Ka-Yi Kelley, Nicholas J. Vinograd, Meghan Perez, Marcelina Chen, Kelly Cohen, Aileen Echiverri Craske, Michelle G. Neuropsychopharmacology Article Dimensional models of anxiety and depression highlight common and distinct symptom clusters that are thought to reflect disruptions in underlying functional processes. The current study investigated how functioning of threat neurocircuitry relates to symptom dimensions of anxiety and depression. Participants were aged 18–19 years (n = 229, 158 female) and were selected to ensure a range of scores on symptom measures. Symptom dimensions of “General Distress” (common to anxiety disorders and depression), “Fears” (more specific to anxiety disorders), and “Anhedonia-apprehension” (more specific to depression) were evaluated. Participants underwent functional magnetic resonance imaging during a Pavlovian fear conditioning paradigm. Multilevel modeling analyses estimated relationships between symptom dimensions and activation in threat neural circuitry. Exploratory whole brain analyses were also conducted. Threat-related neural activity was not associated with General Distress or Fears. Anhedonia-apprehension was associated with activation of bilateral amygdala, anterior insula and dACC during late extinction. We found no evidence to support an association between symptom dimensions of General Distress or Fears with threat circuitry activation in a large sample of young adults. We did, however, find that the symptom dimension of Anhedonia-apprehension was significantly associated with threat-related neural activation during fear extinction. This effect requires replication in future work but may reflect anhedonic impairments in learning when contingencies are altered, possibly linked to the rewarding relief of an unexpectedly absent threat. Springer International Publishing 2021-04-08 2021-08 /pmc/articles/PMC8280223/ /pubmed/33833400 http://dx.doi.org/10.1038/s41386-021-01003-8 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Young, Katherine S.
Bookheimer, Susan Y.
Nusslock, Robin
Zinbarg, Richard E.
Damme, Katherine S. F.
Chat, Iris Ka-Yi
Kelley, Nicholas J.
Vinograd, Meghan
Perez, Marcelina
Chen, Kelly
Cohen, Aileen Echiverri
Craske, Michelle G.
Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title_full Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title_fullStr Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title_full_unstemmed Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title_short Dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
title_sort dysregulation of threat neurocircuitry during fear extinction: the role of anhedonia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280223/
https://www.ncbi.nlm.nih.gov/pubmed/33833400
http://dx.doi.org/10.1038/s41386-021-01003-8
work_keys_str_mv AT youngkatherines dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT bookheimersusany dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT nusslockrobin dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT zinbargricharde dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT dammekatherinesf dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT chatiriskayi dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT kelleynicholasj dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT vinogradmeghan dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT perezmarcelina dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT chenkelly dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT cohenaileenechiverri dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia
AT craskemichelleg dysregulationofthreatneurocircuitryduringfearextinctiontheroleofanhedonia