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Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures

Functional neuroimaging of social stress induction has considerably furthered our understanding of the neural risk architecture of stress‐related mental disorders. However, broad application of existing neuroimaging stress paradigms is challenging, among others due to the relatively high intensity o...

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Autores principales: Fehlner, Phöbe, Bilek, Edda, Harneit, Anais, Böhringer, Andreas, Moessnang, Carolin, Meyer‐Lindenberg, Andreas, Tost, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268032/
https://www.ncbi.nlm.nih.gov/pubmed/31958212
http://dx.doi.org/10.1002/hbm.24932
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author Fehlner, Phöbe
Bilek, Edda
Harneit, Anais
Böhringer, Andreas
Moessnang, Carolin
Meyer‐Lindenberg, Andreas
Tost, Heike
author_facet Fehlner, Phöbe
Bilek, Edda
Harneit, Anais
Böhringer, Andreas
Moessnang, Carolin
Meyer‐Lindenberg, Andreas
Tost, Heike
author_sort Fehlner, Phöbe
collection PubMed
description Functional neuroimaging of social stress induction has considerably furthered our understanding of the neural risk architecture of stress‐related mental disorders. However, broad application of existing neuroimaging stress paradigms is challenging, among others due to the relatively high intensity of the employed stressors, which limits applications in patients and longitudinal study designs. Here, we introduce a less intense neuroimaging stress paradigm in which subjects anticipate, prepare, and give speeches under simulated social evaluation without harsh investigator feedback or provoked performance failures (IMaging Paradigm for Evaluative Social Stress, IMPRESS). We show that IMPRESS significantly increases perceived arousal as well as adrenergic (heart rate, pupil diameter, and blood pressure) and hormonal (cortisol) responses. Amygdala and perigenual anterior cingulate cortex (pACC), two key regions of the emotion and stress regulatory circuitry, are significantly engaged by IMPRESS. We further report associations of amygdala and pACC responses with measures of adrenergic arousal (heart rate, pupil diameter) and social environmental risk factors (adverse childhood experiences, urban living). Our data indicate that IMPRESS induces benchmark psychological and endocrinological responses to social evaluative stress, taps into core neural circuits related to stress processing and mental health risk, and is promising for application in mental illness and in longitudinal study designs.
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spelling pubmed-72680322020-06-12 Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures Fehlner, Phöbe Bilek, Edda Harneit, Anais Böhringer, Andreas Moessnang, Carolin Meyer‐Lindenberg, Andreas Tost, Heike Hum Brain Mapp Research Articles Functional neuroimaging of social stress induction has considerably furthered our understanding of the neural risk architecture of stress‐related mental disorders. However, broad application of existing neuroimaging stress paradigms is challenging, among others due to the relatively high intensity of the employed stressors, which limits applications in patients and longitudinal study designs. Here, we introduce a less intense neuroimaging stress paradigm in which subjects anticipate, prepare, and give speeches under simulated social evaluation without harsh investigator feedback or provoked performance failures (IMaging Paradigm for Evaluative Social Stress, IMPRESS). We show that IMPRESS significantly increases perceived arousal as well as adrenergic (heart rate, pupil diameter, and blood pressure) and hormonal (cortisol) responses. Amygdala and perigenual anterior cingulate cortex (pACC), two key regions of the emotion and stress regulatory circuitry, are significantly engaged by IMPRESS. We further report associations of amygdala and pACC responses with measures of adrenergic arousal (heart rate, pupil diameter) and social environmental risk factors (adverse childhood experiences, urban living). Our data indicate that IMPRESS induces benchmark psychological and endocrinological responses to social evaluative stress, taps into core neural circuits related to stress processing and mental health risk, and is promising for application in mental illness and in longitudinal study designs. John Wiley & Sons, Inc. 2020-01-20 /pmc/articles/PMC7268032/ /pubmed/31958212 http://dx.doi.org/10.1002/hbm.24932 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Fehlner, Phöbe
Bilek, Edda
Harneit, Anais
Böhringer, Andreas
Moessnang, Carolin
Meyer‐Lindenberg, Andreas
Tost, Heike
Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title_full Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title_fullStr Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title_full_unstemmed Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title_short Neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
title_sort neural responses to social evaluative threat in the absence of negative investigator feedback and provoked performance failures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268032/
https://www.ncbi.nlm.nih.gov/pubmed/31958212
http://dx.doi.org/10.1002/hbm.24932
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