Cargando…

Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder

Affective hyper-reactivity and impaired cognitive control of emotional material are core features of borderline personality disorder (BPD). A high percentage of individuals with BPD experience stress-related dissociation, including emotional numbing and memory disruptions. So far little is known abo...

Descripción completa

Detalles Bibliográficos
Autores principales: Krause-Utz, Annegret, Winter, Dorina, Schriner, Friederike, Chiu, Chui-De, Lis, Stefanie, Spinhoven, Philip, Bohus, Martin, Schmahl, Christian, Elzinga, Bernet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956011/
https://www.ncbi.nlm.nih.gov/pubmed/28526931
http://dx.doi.org/10.1007/s00406-017-0806-x
_version_ 1783323809693040640
author Krause-Utz, Annegret
Winter, Dorina
Schriner, Friederike
Chiu, Chui-De
Lis, Stefanie
Spinhoven, Philip
Bohus, Martin
Schmahl, Christian
Elzinga, Bernet M.
author_facet Krause-Utz, Annegret
Winter, Dorina
Schriner, Friederike
Chiu, Chui-De
Lis, Stefanie
Spinhoven, Philip
Bohus, Martin
Schmahl, Christian
Elzinga, Bernet M.
author_sort Krause-Utz, Annegret
collection PubMed
description Affective hyper-reactivity and impaired cognitive control of emotional material are core features of borderline personality disorder (BPD). A high percentage of individuals with BPD experience stress-related dissociation, including emotional numbing and memory disruptions. So far little is known about how dissociation influences the neural processing of emotional material in the context of a working memory task in BPD. We aimed to investigate whole-brain activity and amygdala functional connectivity (FC) during an Emotional Working Memory Task (EWMT) after dissociation induction in un-medicated BPD patients compared to healthy controls (HC). Using script-driven imagery, dissociation was induced in 17 patients (‘BPD_D’), while 12 patients (‘BPD_N’) and 18 HC were exposed to neutral scripts during fMRI. Afterwards, participants performed the EWMT with neutral vs. negative IAPS pictures vs. no distractors. Main outcome measures were behavioral performance (reaction times, errors) and whole-brain activity during the EWMT. Psychophysiological interaction analysis was used to examine amygdala connectivity during emotional distraction. BPD patients after dissociation induction showed overall WM impairments, a deactivation in bilateral amygdala, and lower activity in left cuneus, lingual gyrus, and posterior cingulate than BPD_N, along with stronger left inferior frontal gyrus activity than HC. Furthermore, reduced amygdala FC with fusiform gyrus and stronger amygdala FC with right middle/superior temporal gyrus and left inferior parietal lobule was observed in BPD_D. Findings suggest that dissociation affects reactivity to emotionally salient material and WM. Altered activity in areas associated with emotion processing, memory, and self-referential processes may contribute to dissociative states in BPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00406-017-0806-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5956011
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-59560112018-05-18 Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder Krause-Utz, Annegret Winter, Dorina Schriner, Friederike Chiu, Chui-De Lis, Stefanie Spinhoven, Philip Bohus, Martin Schmahl, Christian Elzinga, Bernet M. Eur Arch Psychiatry Clin Neurosci Original Paper Affective hyper-reactivity and impaired cognitive control of emotional material are core features of borderline personality disorder (BPD). A high percentage of individuals with BPD experience stress-related dissociation, including emotional numbing and memory disruptions. So far little is known about how dissociation influences the neural processing of emotional material in the context of a working memory task in BPD. We aimed to investigate whole-brain activity and amygdala functional connectivity (FC) during an Emotional Working Memory Task (EWMT) after dissociation induction in un-medicated BPD patients compared to healthy controls (HC). Using script-driven imagery, dissociation was induced in 17 patients (‘BPD_D’), while 12 patients (‘BPD_N’) and 18 HC were exposed to neutral scripts during fMRI. Afterwards, participants performed the EWMT with neutral vs. negative IAPS pictures vs. no distractors. Main outcome measures were behavioral performance (reaction times, errors) and whole-brain activity during the EWMT. Psychophysiological interaction analysis was used to examine amygdala connectivity during emotional distraction. BPD patients after dissociation induction showed overall WM impairments, a deactivation in bilateral amygdala, and lower activity in left cuneus, lingual gyrus, and posterior cingulate than BPD_N, along with stronger left inferior frontal gyrus activity than HC. Furthermore, reduced amygdala FC with fusiform gyrus and stronger amygdala FC with right middle/superior temporal gyrus and left inferior parietal lobule was observed in BPD_D. Findings suggest that dissociation affects reactivity to emotionally salient material and WM. Altered activity in areas associated with emotion processing, memory, and self-referential processes may contribute to dissociative states in BPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00406-017-0806-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-05-19 2018 /pmc/articles/PMC5956011/ /pubmed/28526931 http://dx.doi.org/10.1007/s00406-017-0806-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Krause-Utz, Annegret
Winter, Dorina
Schriner, Friederike
Chiu, Chui-De
Lis, Stefanie
Spinhoven, Philip
Bohus, Martin
Schmahl, Christian
Elzinga, Bernet M.
Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title_full Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title_fullStr Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title_full_unstemmed Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title_short Reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
title_sort reduced amygdala reactivity and impaired working memory during dissociation in borderline personality disorder
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956011/
https://www.ncbi.nlm.nih.gov/pubmed/28526931
http://dx.doi.org/10.1007/s00406-017-0806-x
work_keys_str_mv AT krauseutzannegret reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT winterdorina reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT schrinerfriederike reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT chiuchuide reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT lisstefanie reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT spinhovenphilip reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT bohusmartin reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT schmahlchristian reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder
AT elzingabernetm reducedamygdalareactivityandimpairedworkingmemoryduringdissociationinborderlinepersonalitydisorder