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Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry

BACKGROUND: Coordination of activity between the amygdala and ventromedial prefrontal cortex (vmPFC) is important for fear-extinction learning. Aberrant recruitment of this circuitry is associated with anxiety disorders. Here, we sought to determine if individual differences in future threat uncerta...

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Autores principales: Morriss, Jayne, Christakou, Anastasia, van Reekum, Carien M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496864/
https://www.ncbi.nlm.nih.gov/pubmed/26161254
http://dx.doi.org/10.1186/s13587-015-0019-8
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author Morriss, Jayne
Christakou, Anastasia
van Reekum, Carien M.
author_facet Morriss, Jayne
Christakou, Anastasia
van Reekum, Carien M.
author_sort Morriss, Jayne
collection PubMed
description BACKGROUND: Coordination of activity between the amygdala and ventromedial prefrontal cortex (vmPFC) is important for fear-extinction learning. Aberrant recruitment of this circuitry is associated with anxiety disorders. Here, we sought to determine if individual differences in future threat uncertainty sensitivity, a potential risk factor for anxiety disorders, underly compromised recruitment of fear extinction circuitry. Twenty-two healthy subjects completed a cued fear conditioning task with acquisition and extinction phases. During the task, pupil dilation, skin conductance response, and functional magnetic resonance imaging were acquired. We assessed the temporality of fear extinction learning by splitting the extinction phase into early and late extinction. Threat uncertainty sensitivity was measured using self-reported intolerance of uncertainty (IU). RESULTS: During early extinction learning, we found low IU scores to be associated with larger skin conductance responses and right amygdala activity to learned threat vs. safety cues, whereas high IU scores were associated with no skin conductance discrimination and greater activity within the right amygdala to previously learned safety cues. In late extinction learning, low IU scores were associated with successful inhibition of previously learned threat, reflected in comparable skin conductance response and right amgydala activity to learned threat vs. safety cues, whilst high IU scores were associated with continued fear expression to learned threat, indexed by larger skin conductance and amygdala activity to threat vs. safety cues. In addition, high IU scores were associated with greater vmPFC activity to threat vs. safety cues in late extinction. Similar patterns of IU and extinction learning were found for pupil dilation. The results were specific for IU and did not generalize to self-reported trait anxiety. CONCLUSIONS: Overall, the neural and psychophysiological patterns observed here suggest high IU individuals to disproportionately generalize threat during times of uncertainty, which subsequently compromises fear extinction learning. More broadly, these findings highlight the potential of intolerance of uncertainty-based mechanisms to help understand pathological fear in anxiety disorders and inform potential treatment targets.
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spelling pubmed-44968642015-07-10 Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry Morriss, Jayne Christakou, Anastasia van Reekum, Carien M. Biol Mood Anxiety Disord Research BACKGROUND: Coordination of activity between the amygdala and ventromedial prefrontal cortex (vmPFC) is important for fear-extinction learning. Aberrant recruitment of this circuitry is associated with anxiety disorders. Here, we sought to determine if individual differences in future threat uncertainty sensitivity, a potential risk factor for anxiety disorders, underly compromised recruitment of fear extinction circuitry. Twenty-two healthy subjects completed a cued fear conditioning task with acquisition and extinction phases. During the task, pupil dilation, skin conductance response, and functional magnetic resonance imaging were acquired. We assessed the temporality of fear extinction learning by splitting the extinction phase into early and late extinction. Threat uncertainty sensitivity was measured using self-reported intolerance of uncertainty (IU). RESULTS: During early extinction learning, we found low IU scores to be associated with larger skin conductance responses and right amygdala activity to learned threat vs. safety cues, whereas high IU scores were associated with no skin conductance discrimination and greater activity within the right amygdala to previously learned safety cues. In late extinction learning, low IU scores were associated with successful inhibition of previously learned threat, reflected in comparable skin conductance response and right amgydala activity to learned threat vs. safety cues, whilst high IU scores were associated with continued fear expression to learned threat, indexed by larger skin conductance and amygdala activity to threat vs. safety cues. In addition, high IU scores were associated with greater vmPFC activity to threat vs. safety cues in late extinction. Similar patterns of IU and extinction learning were found for pupil dilation. The results were specific for IU and did not generalize to self-reported trait anxiety. CONCLUSIONS: Overall, the neural and psychophysiological patterns observed here suggest high IU individuals to disproportionately generalize threat during times of uncertainty, which subsequently compromises fear extinction learning. More broadly, these findings highlight the potential of intolerance of uncertainty-based mechanisms to help understand pathological fear in anxiety disorders and inform potential treatment targets. BioMed Central 2015-07-10 /pmc/articles/PMC4496864/ /pubmed/26161254 http://dx.doi.org/10.1186/s13587-015-0019-8 Text en © Morriss et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Morriss, Jayne
Christakou, Anastasia
van Reekum, Carien M.
Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title_full Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title_fullStr Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title_full_unstemmed Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title_short Intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
title_sort intolerance of uncertainty predicts fear extinction in amygdala-ventromedial prefrontal cortical circuitry
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496864/
https://www.ncbi.nlm.nih.gov/pubmed/26161254
http://dx.doi.org/10.1186/s13587-015-0019-8
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