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Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder
Childhood trauma is believed to contribute to the development of borderline personality disorder (BPD), however the mechanism by which childhood trauma increases risk for specific symptoms of the disorder is not well understood. Here, we explore the relationship between childhood trauma, brain activ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471284/ https://www.ncbi.nlm.nih.gov/pubmed/25942040 http://dx.doi.org/10.1038/tp.2015.53 |
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author | Nicol, K Pope, M Romaniuk, L Hall, J |
author_facet | Nicol, K Pope, M Romaniuk, L Hall, J |
author_sort | Nicol, K |
collection | PubMed |
description | Childhood trauma is believed to contribute to the development of borderline personality disorder (BPD), however the mechanism by which childhood trauma increases risk for specific symptoms of the disorder is not well understood. Here, we explore the relationship between childhood trauma, brain activation in response to emotional stimuli and psychotic symptoms in BPD. Twenty individuals with a diagnosis of BPD and 16 healthy controls were recruited to undergo a functional MRI scan, during which they viewed images of faces expressing the emotion of fear. Participants also completed the childhood trauma questionnaire (CTQ) and a structured clinical interview. Between-group differences in brain activation to fearful faces were limited to decreased activation in the BPD group in the right cuneus. However, within the BPD group, there was a significant positive correlation between physical abuse scores on the CTQ and BOLD signal in the midbrain, pulvinar and medial frontal gyrus to fearful (versus neutral) faces. In addition there was a significant correlation between midbrain activation and reported psychotic symptoms in the BPD group (P<0.05). These results show that physical abuse in childhood is, in individuals with BPD, associated with significantly increased activation of a network of brain regions including the midbrain in response to emotional stimuli. Sustained differences in the response of the midbrain to emotional stimuli in individuals with BPD who suffered childhood physical abuse may underlie the vulnerability of these patients to developing psychotic symptoms. |
format | Online Article Text |
id | pubmed-4471284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44712842015-06-24 Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder Nicol, K Pope, M Romaniuk, L Hall, J Transl Psychiatry Original Article Childhood trauma is believed to contribute to the development of borderline personality disorder (BPD), however the mechanism by which childhood trauma increases risk for specific symptoms of the disorder is not well understood. Here, we explore the relationship between childhood trauma, brain activation in response to emotional stimuli and psychotic symptoms in BPD. Twenty individuals with a diagnosis of BPD and 16 healthy controls were recruited to undergo a functional MRI scan, during which they viewed images of faces expressing the emotion of fear. Participants also completed the childhood trauma questionnaire (CTQ) and a structured clinical interview. Between-group differences in brain activation to fearful faces were limited to decreased activation in the BPD group in the right cuneus. However, within the BPD group, there was a significant positive correlation between physical abuse scores on the CTQ and BOLD signal in the midbrain, pulvinar and medial frontal gyrus to fearful (versus neutral) faces. In addition there was a significant correlation between midbrain activation and reported psychotic symptoms in the BPD group (P<0.05). These results show that physical abuse in childhood is, in individuals with BPD, associated with significantly increased activation of a network of brain regions including the midbrain in response to emotional stimuli. Sustained differences in the response of the midbrain to emotional stimuli in individuals with BPD who suffered childhood physical abuse may underlie the vulnerability of these patients to developing psychotic symptoms. Nature Publishing Group 2015-05 2015-05-05 /pmc/articles/PMC4471284/ /pubmed/25942040 http://dx.doi.org/10.1038/tp.2015.53 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Nicol, K Pope, M Romaniuk, L Hall, J Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title | Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title_full | Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title_fullStr | Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title_full_unstemmed | Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title_short | Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
title_sort | childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471284/ https://www.ncbi.nlm.nih.gov/pubmed/25942040 http://dx.doi.org/10.1038/tp.2015.53 |
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