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Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder
Post-traumatic stress disorder (PTSD), obsessive–compulsive disorder (OCD), and social anxiety disorder (SAD) all bear the core symptom of anxiety and are separately classified in the new DSM-5 system. The aim of the present study is to obtain evidence for neuroanatomical difference for these disord...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542504/ https://www.ncbi.nlm.nih.gov/pubmed/26347628 http://dx.doi.org/10.3389/fnbeh.2015.00219 |
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author | Cheng, Bochao Huang, Xiaoqi Li, Shiguang Hu, Xinyu Luo, Ya Wang, Xiuli Yang, Xun Qiu, Changjian Yang, Yanchun Zhang, Wei Bi, Feng Roberts, Neil Gong, Qiyong |
author_facet | Cheng, Bochao Huang, Xiaoqi Li, Shiguang Hu, Xinyu Luo, Ya Wang, Xiuli Yang, Xun Qiu, Changjian Yang, Yanchun Zhang, Wei Bi, Feng Roberts, Neil Gong, Qiyong |
author_sort | Cheng, Bochao |
collection | PubMed |
description | Post-traumatic stress disorder (PTSD), obsessive–compulsive disorder (OCD), and social anxiety disorder (SAD) all bear the core symptom of anxiety and are separately classified in the new DSM-5 system. The aim of the present study is to obtain evidence for neuroanatomical difference for these disorders. We applied voxel-based morphometry (VBM) with Diffeomorphic Anatomical Registration Through Exponentiated Lie to compare gray matter volume (GMV) in magnetic resonance images obtained for 30 patients with PTSD, 29 patients with OCD, 20 patients with SAD, and 30 healthy controls. GMV across all four groups differed in left hypothalamus and left inferior parietal lobule and post hoc analyses revealed that this difference is primarily due to reduced GMV in the PTSD group relative to the other groups. Further analysis revealed that the PTSD group also showed reduced GMV in frontal lobe, temporal lobe, and cerebellum compared to the OCD group, and reduced GMV in frontal lobes bilaterally compared to SAD group. A significant negative correlation with anxiety symptoms is observed for GMV in left hypothalamus in three disorder groups. We have thus found evidence for brain structure differences that in future could provide biomarkers to potentially support classification of these disorders using MRI. |
format | Online Article Text |
id | pubmed-4542504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45425042015-09-07 Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder Cheng, Bochao Huang, Xiaoqi Li, Shiguang Hu, Xinyu Luo, Ya Wang, Xiuli Yang, Xun Qiu, Changjian Yang, Yanchun Zhang, Wei Bi, Feng Roberts, Neil Gong, Qiyong Front Behav Neurosci Neuroscience Post-traumatic stress disorder (PTSD), obsessive–compulsive disorder (OCD), and social anxiety disorder (SAD) all bear the core symptom of anxiety and are separately classified in the new DSM-5 system. The aim of the present study is to obtain evidence for neuroanatomical difference for these disorders. We applied voxel-based morphometry (VBM) with Diffeomorphic Anatomical Registration Through Exponentiated Lie to compare gray matter volume (GMV) in magnetic resonance images obtained for 30 patients with PTSD, 29 patients with OCD, 20 patients with SAD, and 30 healthy controls. GMV across all four groups differed in left hypothalamus and left inferior parietal lobule and post hoc analyses revealed that this difference is primarily due to reduced GMV in the PTSD group relative to the other groups. Further analysis revealed that the PTSD group also showed reduced GMV in frontal lobe, temporal lobe, and cerebellum compared to the OCD group, and reduced GMV in frontal lobes bilaterally compared to SAD group. A significant negative correlation with anxiety symptoms is observed for GMV in left hypothalamus in three disorder groups. We have thus found evidence for brain structure differences that in future could provide biomarkers to potentially support classification of these disorders using MRI. Frontiers Media S.A. 2015-08-20 /pmc/articles/PMC4542504/ /pubmed/26347628 http://dx.doi.org/10.3389/fnbeh.2015.00219 Text en Copyright © 2015 Cheng, Huang, Li, Hu, Luo, Wang, Yang, Qiu, Yang, Zhang, Bi, Roberts and Gong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Cheng, Bochao Huang, Xiaoqi Li, Shiguang Hu, Xinyu Luo, Ya Wang, Xiuli Yang, Xun Qiu, Changjian Yang, Yanchun Zhang, Wei Bi, Feng Roberts, Neil Gong, Qiyong Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title | Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title_full | Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title_fullStr | Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title_full_unstemmed | Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title_short | Gray Matter Alterations in Post-Traumatic Stress Disorder, Obsessive–Compulsive Disorder, and Social Anxiety Disorder |
title_sort | gray matter alterations in post-traumatic stress disorder, obsessive–compulsive disorder, and social anxiety disorder |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542504/ https://www.ncbi.nlm.nih.gov/pubmed/26347628 http://dx.doi.org/10.3389/fnbeh.2015.00219 |
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