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Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder
The hippocampus, a key structure with distinct subfield functions, is strongly implicated in the pathophysiology of post-traumatic stress disorder (PTSD); however, few studies of hippocampus subfields in PTSD have focused on pediatric patients. We therefore investigated the hippocampal subfield volu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943370/ https://www.ncbi.nlm.nih.gov/pubmed/33315100 http://dx.doi.org/10.1093/scan/nsaa162 |
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author | Li, Lei Pan, Nanfang Zhang, Lianqing Lui, Su Huang, Xiaoqi Xu, Xin Wang, Song Lei, Du Li, Lingjiang Kemp, Graham J Gong, Qiyong |
author_facet | Li, Lei Pan, Nanfang Zhang, Lianqing Lui, Su Huang, Xiaoqi Xu, Xin Wang, Song Lei, Du Li, Lingjiang Kemp, Graham J Gong, Qiyong |
author_sort | Li, Lei |
collection | PubMed |
description | The hippocampus, a key structure with distinct subfield functions, is strongly implicated in the pathophysiology of post-traumatic stress disorder (PTSD); however, few studies of hippocampus subfields in PTSD have focused on pediatric patients. We therefore investigated the hippocampal subfield volume using an automated segmentation method and explored the subfield-centered functional connectivity aberrations related to the anatomical changes, in a homogenous population of traumatized children with and without PTSD. To investigate the potential diagnostic value in individual patients, we used a machine learning approach to identify features with significant discriminative power for diagnosis of PTSD using random forest classifiers. Compared to controls, we found significant mean volume reductions of 8.4% and 9.7% in the right presubiculum and hippocampal tail in patients, respectively. These two subfields’ volumes were the most significant contributors to group discrimination, with a mean classification accuracy of 69% and a specificity of 81%. These anatomical alterations, along with the altered functional connectivity between (pre)subiculum and inferior frontal gyrus, may underlie deficits in fear circuitry leading to dysfunction of fear extinction and episodic memory, causally important in post-traumatic symptoms such as hypervigilance and re-experience. For the first time, we suggest that hippocampal subfield volumes might be useful in discriminating traumatized children with and without PTSD. |
format | Online Article Text |
id | pubmed-7943370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79433702021-03-15 Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder Li, Lei Pan, Nanfang Zhang, Lianqing Lui, Su Huang, Xiaoqi Xu, Xin Wang, Song Lei, Du Li, Lingjiang Kemp, Graham J Gong, Qiyong Soc Cogn Affect Neurosci Original Manuscript The hippocampus, a key structure with distinct subfield functions, is strongly implicated in the pathophysiology of post-traumatic stress disorder (PTSD); however, few studies of hippocampus subfields in PTSD have focused on pediatric patients. We therefore investigated the hippocampal subfield volume using an automated segmentation method and explored the subfield-centered functional connectivity aberrations related to the anatomical changes, in a homogenous population of traumatized children with and without PTSD. To investigate the potential diagnostic value in individual patients, we used a machine learning approach to identify features with significant discriminative power for diagnosis of PTSD using random forest classifiers. Compared to controls, we found significant mean volume reductions of 8.4% and 9.7% in the right presubiculum and hippocampal tail in patients, respectively. These two subfields’ volumes were the most significant contributors to group discrimination, with a mean classification accuracy of 69% and a specificity of 81%. These anatomical alterations, along with the altered functional connectivity between (pre)subiculum and inferior frontal gyrus, may underlie deficits in fear circuitry leading to dysfunction of fear extinction and episodic memory, causally important in post-traumatic symptoms such as hypervigilance and re-experience. For the first time, we suggest that hippocampal subfield volumes might be useful in discriminating traumatized children with and without PTSD. Oxford University Press 2020-12-14 /pmc/articles/PMC7943370/ /pubmed/33315100 http://dx.doi.org/10.1093/scan/nsaa162 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Manuscript Li, Lei Pan, Nanfang Zhang, Lianqing Lui, Su Huang, Xiaoqi Xu, Xin Wang, Song Lei, Du Li, Lingjiang Kemp, Graham J Gong, Qiyong Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title | Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title_full | Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title_fullStr | Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title_full_unstemmed | Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title_short | Hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
title_sort | hippocampal subfield alterations in pediatric patients with post-traumatic stress disorder |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943370/ https://www.ncbi.nlm.nih.gov/pubmed/33315100 http://dx.doi.org/10.1093/scan/nsaa162 |
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