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The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety

Theoretical accounts have linked anxiety to intolerance of ambiguity. However, this relationship has not been well operationalized empirically. Here, we used computational and neuro-imaging methods to characterize anxiety-related differences in aversive decision-making under ambiguity and associated...

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Autores principales: LAWRANCE, EMMA L., GAGNE, CHRISTOPHER R., O’REILLY, JILL X., BIJSTERBOSCH, JANINE, BISHOP, SONIA J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223033/
https://www.ncbi.nlm.nih.gov/pubmed/35757373
http://dx.doi.org/10.5334/cpsy.67
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author LAWRANCE, EMMA L.
GAGNE, CHRISTOPHER R.
O’REILLY, JILL X.
BIJSTERBOSCH, JANINE
BISHOP, SONIA J.
author_facet LAWRANCE, EMMA L.
GAGNE, CHRISTOPHER R.
O’REILLY, JILL X.
BIJSTERBOSCH, JANINE
BISHOP, SONIA J.
author_sort LAWRANCE, EMMA L.
collection PubMed
description Theoretical accounts have linked anxiety to intolerance of ambiguity. However, this relationship has not been well operationalized empirically. Here, we used computational and neuro-imaging methods to characterize anxiety-related differences in aversive decision-making under ambiguity and associated patterns of cortical activity. Adult human participants chose between two urns on each trial. The ratio of tokens (‘O’s and ‘X’s) in each urn determined probability of electrical stimulation receipt. A number above each urn indicated the magnitude of stimulation that would be received if a shock was delivered. On ambiguous trials, one of the two urns had tokens occluded. By varying the number of tokens occluded, we manipulated the extent of missing information. At higher levels of missing information, there is greater second order uncertainty, i.e., more uncertainty as to the probability of pulling a given type of token from the urn. Adult human participants demonstrated avoidance of ambiguous options which increased with level of missing information. Extent of ‘information-level dependent’ ambiguity aversion was significantly positively correlated with trait anxiety. Activity in both the dorsal anterior cingulate cortex and inferior frontal sulcus during the decision-making period increased as a function of missing information. Greater engagement of these regions, on high missing information trials, was observed when participants went on to select the ambiguous option; this was especially apparent in high trait anxious individuals. These findings are consistent with individuals vulnerable to anxiety requiring greater activation of frontal regions supporting rational decision-making to overcome a predisposition to engage in ambiguity avoidance at high levels of missing information.
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spelling pubmed-92230332022-06-23 The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety LAWRANCE, EMMA L. GAGNE, CHRISTOPHER R. O’REILLY, JILL X. BIJSTERBOSCH, JANINE BISHOP, SONIA J. Comput Psychiatr Article Theoretical accounts have linked anxiety to intolerance of ambiguity. However, this relationship has not been well operationalized empirically. Here, we used computational and neuro-imaging methods to characterize anxiety-related differences in aversive decision-making under ambiguity and associated patterns of cortical activity. Adult human participants chose between two urns on each trial. The ratio of tokens (‘O’s and ‘X’s) in each urn determined probability of electrical stimulation receipt. A number above each urn indicated the magnitude of stimulation that would be received if a shock was delivered. On ambiguous trials, one of the two urns had tokens occluded. By varying the number of tokens occluded, we manipulated the extent of missing information. At higher levels of missing information, there is greater second order uncertainty, i.e., more uncertainty as to the probability of pulling a given type of token from the urn. Adult human participants demonstrated avoidance of ambiguous options which increased with level of missing information. Extent of ‘information-level dependent’ ambiguity aversion was significantly positively correlated with trait anxiety. Activity in both the dorsal anterior cingulate cortex and inferior frontal sulcus during the decision-making period increased as a function of missing information. Greater engagement of these regions, on high missing information trials, was observed when participants went on to select the ambiguous option; this was especially apparent in high trait anxious individuals. These findings are consistent with individuals vulnerable to anxiety requiring greater activation of frontal regions supporting rational decision-making to overcome a predisposition to engage in ambiguity avoidance at high levels of missing information. 2022 2022-02-03 /pmc/articles/PMC9223033/ /pubmed/35757373 http://dx.doi.org/10.5334/cpsy.67 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
LAWRANCE, EMMA L.
GAGNE, CHRISTOPHER R.
O’REILLY, JILL X.
BIJSTERBOSCH, JANINE
BISHOP, SONIA J.
The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title_full The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title_fullStr The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title_full_unstemmed The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title_short The Computational and Neural Substrates of Ambiguity Avoidance in Anxiety
title_sort computational and neural substrates of ambiguity avoidance in anxiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223033/
https://www.ncbi.nlm.nih.gov/pubmed/35757373
http://dx.doi.org/10.5334/cpsy.67
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