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Neural sensitivity to social reward and punishment anticipation in social anxiety disorder

An imbalance in the neural motivational system may underlie Social Anxiety Disorder (SAD). This study examines social reward and punishment anticipation in SAD, predicting a valence-specific effect: increased striatal activity for punishment avoidance compared to obtaining a reward. Individuals with...

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Autores principales: Cremers, Henk R., Veer, Ilya M., Spinhoven, Philip, Rombouts, Serge A. R. B., Roelofs, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283602/
https://www.ncbi.nlm.nih.gov/pubmed/25601830
http://dx.doi.org/10.3389/fnbeh.2014.00439
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author Cremers, Henk R.
Veer, Ilya M.
Spinhoven, Philip
Rombouts, Serge A. R. B.
Roelofs, Karin
author_facet Cremers, Henk R.
Veer, Ilya M.
Spinhoven, Philip
Rombouts, Serge A. R. B.
Roelofs, Karin
author_sort Cremers, Henk R.
collection PubMed
description An imbalance in the neural motivational system may underlie Social Anxiety Disorder (SAD). This study examines social reward and punishment anticipation in SAD, predicting a valence-specific effect: increased striatal activity for punishment avoidance compared to obtaining a reward. Individuals with SAD (n = 20) and age, gender, and education case-matched controls (n = 20) participated in a functional magnetic resonance imaging (fMRI) study. During fMRI scanning, participants performed a Social Incentive Delay (SID) task to measure the anticipation of social reward and punishment. The left putamen (part of the striatum) showed a valence-specific interaction with group after correcting for medication use and comorbidity. The control group showed a relatively stronger activation for reward vs. punishment trials, compared to the social anxiety group. However, post-hoc pairwise comparisons were not significant, indicating that the effect is driven by a relative difference. A connectivity analysis (Psychophysiological interaction) further revealed a general salience effect: SAD patients showed decreased putamen-ACC connectivity compared to controls for both reward and punishment trials. Together these results suggest that the usual motivational preference for social reward is absent in SAD. In addition, cortical control processes during social incentive anticipation may be disrupted in SAD. These results provide initial evidence for altered striatal involvement in both valence-specific and valence-nonspecific processing of social incentives, and stress the relevance of taking motivational processes into account when studying social anxiety.
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spelling pubmed-42836022015-01-19 Neural sensitivity to social reward and punishment anticipation in social anxiety disorder Cremers, Henk R. Veer, Ilya M. Spinhoven, Philip Rombouts, Serge A. R. B. Roelofs, Karin Front Behav Neurosci Neuroscience An imbalance in the neural motivational system may underlie Social Anxiety Disorder (SAD). This study examines social reward and punishment anticipation in SAD, predicting a valence-specific effect: increased striatal activity for punishment avoidance compared to obtaining a reward. Individuals with SAD (n = 20) and age, gender, and education case-matched controls (n = 20) participated in a functional magnetic resonance imaging (fMRI) study. During fMRI scanning, participants performed a Social Incentive Delay (SID) task to measure the anticipation of social reward and punishment. The left putamen (part of the striatum) showed a valence-specific interaction with group after correcting for medication use and comorbidity. The control group showed a relatively stronger activation for reward vs. punishment trials, compared to the social anxiety group. However, post-hoc pairwise comparisons were not significant, indicating that the effect is driven by a relative difference. A connectivity analysis (Psychophysiological interaction) further revealed a general salience effect: SAD patients showed decreased putamen-ACC connectivity compared to controls for both reward and punishment trials. Together these results suggest that the usual motivational preference for social reward is absent in SAD. In addition, cortical control processes during social incentive anticipation may be disrupted in SAD. These results provide initial evidence for altered striatal involvement in both valence-specific and valence-nonspecific processing of social incentives, and stress the relevance of taking motivational processes into account when studying social anxiety. Frontiers Media S.A. 2015-01-05 /pmc/articles/PMC4283602/ /pubmed/25601830 http://dx.doi.org/10.3389/fnbeh.2014.00439 Text en Copyright © 2015 Cremers, Veer, Spinhoven, Rombouts and Roelofs. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Cremers, Henk R.
Veer, Ilya M.
Spinhoven, Philip
Rombouts, Serge A. R. B.
Roelofs, Karin
Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title_full Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title_fullStr Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title_full_unstemmed Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title_short Neural sensitivity to social reward and punishment anticipation in social anxiety disorder
title_sort neural sensitivity to social reward and punishment anticipation in social anxiety disorder
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283602/
https://www.ncbi.nlm.nih.gov/pubmed/25601830
http://dx.doi.org/10.3389/fnbeh.2014.00439
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