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Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse

Exposure to childhood adverse events is associated with severe consequences for general health and structural and functional changes in the brain of its survivors. In order to unravel and in the end influence the pathway linking adversity and pathology, neuroimaging research is crucial. Up till now...

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Autores principales: Rinne-Albers, Mirjam A., Boateng, Charlotte P., van der Werff, Steven J., Lamers-Winkelman, Francien, Rombouts, Serge A., Vermeiren, Robert R., van der Wee, Nic J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039962/
https://www.ncbi.nlm.nih.gov/pubmed/32094427
http://dx.doi.org/10.1038/s41598-020-60256-3
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author Rinne-Albers, Mirjam A.
Boateng, Charlotte P.
van der Werff, Steven J.
Lamers-Winkelman, Francien
Rombouts, Serge A.
Vermeiren, Robert R.
van der Wee, Nic J.
author_facet Rinne-Albers, Mirjam A.
Boateng, Charlotte P.
van der Werff, Steven J.
Lamers-Winkelman, Francien
Rombouts, Serge A.
Vermeiren, Robert R.
van der Wee, Nic J.
author_sort Rinne-Albers, Mirjam A.
collection PubMed
description Exposure to childhood adverse events is associated with severe consequences for general health and structural and functional changes in the brain of its survivors. In order to unravel and in the end influence the pathway linking adversity and pathology, neuroimaging research is crucial. Up till now studies in minors are scarce and differ in type of adversity or methodology. Almost all studies report lower cortical thickness, but in a broad variety of regions. In this study we investigated cortical thickness measures and clinical data in a well circumscribed group of adolescents with PTSD related to childhood sexual abuse (CSA) (N = 21) and a healthy non-traumatised control group (N = 21). The ventromedial PFC (vmPFC), ACC, insula, and middle/superior temporal gyrus were chosen as ROI’s due to their respective roles in emotion and information processing. No significant effect of group was found for cortical thickness, surface area or volume in any of the ROIs. This is in line with the results of research in adult women with sexual abuse related PTSD, suggesting that this may be specific to this group, independent of age. Recent research points to differential biological and pathological consequences of different types of childhood adversity.
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spelling pubmed-70399622020-02-28 Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse Rinne-Albers, Mirjam A. Boateng, Charlotte P. van der Werff, Steven J. Lamers-Winkelman, Francien Rombouts, Serge A. Vermeiren, Robert R. van der Wee, Nic J. Sci Rep Article Exposure to childhood adverse events is associated with severe consequences for general health and structural and functional changes in the brain of its survivors. In order to unravel and in the end influence the pathway linking adversity and pathology, neuroimaging research is crucial. Up till now studies in minors are scarce and differ in type of adversity or methodology. Almost all studies report lower cortical thickness, but in a broad variety of regions. In this study we investigated cortical thickness measures and clinical data in a well circumscribed group of adolescents with PTSD related to childhood sexual abuse (CSA) (N = 21) and a healthy non-traumatised control group (N = 21). The ventromedial PFC (vmPFC), ACC, insula, and middle/superior temporal gyrus were chosen as ROI’s due to their respective roles in emotion and information processing. No significant effect of group was found for cortical thickness, surface area or volume in any of the ROIs. This is in line with the results of research in adult women with sexual abuse related PTSD, suggesting that this may be specific to this group, independent of age. Recent research points to differential biological and pathological consequences of different types of childhood adversity. Nature Publishing Group UK 2020-02-24 /pmc/articles/PMC7039962/ /pubmed/32094427 http://dx.doi.org/10.1038/s41598-020-60256-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rinne-Albers, Mirjam A.
Boateng, Charlotte P.
van der Werff, Steven J.
Lamers-Winkelman, Francien
Rombouts, Serge A.
Vermeiren, Robert R.
van der Wee, Nic J.
Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title_full Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title_fullStr Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title_full_unstemmed Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title_short Preserved cortical thickness, surface area and volume in adolescents with PTSD after childhood sexual abuse
title_sort preserved cortical thickness, surface area and volume in adolescents with ptsd after childhood sexual abuse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039962/
https://www.ncbi.nlm.nih.gov/pubmed/32094427
http://dx.doi.org/10.1038/s41598-020-60256-3
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