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Attenuated neuronal and autonomic responses during error processing in anorexia nervosa

INTRODUCTION: Anorexia nervosa (AN) is a severe psychiatric illness with alarming mortality rates. Nevertheless, despite former and recent research results, the etiology of AN is still poorly understood. Of particular interest is that, despite exaggerated response control and increased perfectionism...

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Autores principales: Suttkus, Stefanie, Schumann, Andy, De la Cruz, Feliberto, Bär, Karl‐Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413769/
https://www.ncbi.nlm.nih.gov/pubmed/34318622
http://dx.doi.org/10.1002/brb3.2235
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author Suttkus, Stefanie
Schumann, Andy
De la Cruz, Feliberto
Bär, Karl‐Jürgen
author_facet Suttkus, Stefanie
Schumann, Andy
De la Cruz, Feliberto
Bär, Karl‐Jürgen
author_sort Suttkus, Stefanie
collection PubMed
description INTRODUCTION: Anorexia nervosa (AN) is a severe psychiatric illness with alarming mortality rates. Nevertheless, despite former and recent research results, the etiology of AN is still poorly understood. Of particular interest is that, despite exaggerated response control and increased perfectionism scores, patients with AN seem not to perform better that those unaffected in tasks that require inhibitory control. One reason might be aberrant processing of errors. The objective of our study was thus to obtain further insight into the pathopsychology of AN. We were particularly interested in neuronal and autonomic responses during error processing and their association with behavior. METHODS: We analyzed 16 acute patients suffering from restrictive type AN and 21 healthy controls using functional magnetic resonance imaging (fMRI) with simultaneous physiological recordings during a Go/Nogo response inhibition task. Data were corrected for noise due to cardiac and respiratory influence. RESULTS: Patients and controls had similarly successful response inhibition in Nogo trials. However, in failed Nogo trials, controls had significantly greater skin conductance responses (SCR) than in correct Nogo trials. Patients did not exhibit elevated SCR to errors. Furthermore, we found significantly increased neuronal responses, especially in the amygdala and hippocampus, in controls compared to patients during error trials. We also found significant positive correlations in controls but not in patients between Nogo performance and activation in the salience network core regions after errors. CONCLUSION: Acute restrictive type AN patients seem to lack neuronal and autonomic responses to errors that might impede a flexible behavior adaption.
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spelling pubmed-84137692021-09-07 Attenuated neuronal and autonomic responses during error processing in anorexia nervosa Suttkus, Stefanie Schumann, Andy De la Cruz, Feliberto Bär, Karl‐Jürgen Brain Behav Original Research INTRODUCTION: Anorexia nervosa (AN) is a severe psychiatric illness with alarming mortality rates. Nevertheless, despite former and recent research results, the etiology of AN is still poorly understood. Of particular interest is that, despite exaggerated response control and increased perfectionism scores, patients with AN seem not to perform better that those unaffected in tasks that require inhibitory control. One reason might be aberrant processing of errors. The objective of our study was thus to obtain further insight into the pathopsychology of AN. We were particularly interested in neuronal and autonomic responses during error processing and their association with behavior. METHODS: We analyzed 16 acute patients suffering from restrictive type AN and 21 healthy controls using functional magnetic resonance imaging (fMRI) with simultaneous physiological recordings during a Go/Nogo response inhibition task. Data were corrected for noise due to cardiac and respiratory influence. RESULTS: Patients and controls had similarly successful response inhibition in Nogo trials. However, in failed Nogo trials, controls had significantly greater skin conductance responses (SCR) than in correct Nogo trials. Patients did not exhibit elevated SCR to errors. Furthermore, we found significantly increased neuronal responses, especially in the amygdala and hippocampus, in controls compared to patients during error trials. We also found significant positive correlations in controls but not in patients between Nogo performance and activation in the salience network core regions after errors. CONCLUSION: Acute restrictive type AN patients seem to lack neuronal and autonomic responses to errors that might impede a flexible behavior adaption. John Wiley and Sons Inc. 2021-07-28 /pmc/articles/PMC8413769/ /pubmed/34318622 http://dx.doi.org/10.1002/brb3.2235 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Suttkus, Stefanie
Schumann, Andy
De la Cruz, Feliberto
Bär, Karl‐Jürgen
Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title_full Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title_fullStr Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title_full_unstemmed Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title_short Attenuated neuronal and autonomic responses during error processing in anorexia nervosa
title_sort attenuated neuronal and autonomic responses during error processing in anorexia nervosa
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413769/
https://www.ncbi.nlm.nih.gov/pubmed/34318622
http://dx.doi.org/10.1002/brb3.2235
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