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Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()

A variety of structural abnormalities have been described in post traumatic stress disorder (PTSD), but only a few studies have focused on cortical thickness alterations in recent onset PTSD. In this study, we adopted surface-based morphometry (SBM), which enables an exploration of global structural...

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Autores principales: Qi, Shun, Mu, Yunfeng, Liu, Kang, Zhang, Jian, Huan, Yi, Tan, Qingrong, Shi, Mei, Wang, Qiang, Chen, Yunchun, Wang, Huaihai, Wang, Huaning, Zhang, Nanyin, Zhang, Xiaoliang, Xiong, Lize, Yin, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815016/
https://www.ncbi.nlm.nih.gov/pubmed/24273707
http://dx.doi.org/10.1016/j.nicl.2013.08.013
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author Qi, Shun
Mu, Yunfeng
Liu, Kang
Zhang, Jian
Huan, Yi
Tan, Qingrong
Shi, Mei
Wang, Qiang
Chen, Yunchun
Wang, Huaihai
Wang, Huaning
Zhang, Nanyin
Zhang, Xiaoliang
Xiong, Lize
Yin, Hong
author_facet Qi, Shun
Mu, Yunfeng
Liu, Kang
Zhang, Jian
Huan, Yi
Tan, Qingrong
Shi, Mei
Wang, Qiang
Chen, Yunchun
Wang, Huaihai
Wang, Huaning
Zhang, Nanyin
Zhang, Xiaoliang
Xiong, Lize
Yin, Hong
author_sort Qi, Shun
collection PubMed
description A variety of structural abnormalities have been described in post traumatic stress disorder (PTSD), but only a few studies have focused on cortical thickness alterations in recent onset PTSD. In this study, we adopted surface-based morphometry (SBM), which enables an exploration of global structural changes throughout the brain, in order to compare cortical thickness alterations in recent onset PTSD patients, trauma-exposed subjects but without PTSD, and normal controls. Moreover, we used region of interest (ROI) partial correlation analysis to evaluate the correlation among PTSD symptom severity and significant changes of cortical thickness. The widespread cortical thickness reduction relative to the normal controls were found in bilateral inferior and superior parietal lobes, frontal lobes, hippocampus, cingulate cortex, and right lateral occipital lobes in trauma survivors, whereas cortical thickness was only increased in left calcarine cortex in PTSD group. The average cortical thickness of hippocampus and cingulate cortex decreased by 10.75% and 9.09% in PTSD, 3.48% and 2.86% in non PTSD. We further demonstrated that the cortical thicknesses of bilateral ACC and PCC, superior frontal lobes, and hippocampus are negatively correlated with CAPS scores in all trauma survivors. Our study results suggest that stress widens cortical thinning regions and causes more serious effect in recent onset PTSD than non PTSD. It also shows that the cortical thinning in recent onset PTSD predicts the symptom severity.
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spelling pubmed-38150162013-11-22 Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure() Qi, Shun Mu, Yunfeng Liu, Kang Zhang, Jian Huan, Yi Tan, Qingrong Shi, Mei Wang, Qiang Chen, Yunchun Wang, Huaihai Wang, Huaning Zhang, Nanyin Zhang, Xiaoliang Xiong, Lize Yin, Hong Neuroimage Clin Article A variety of structural abnormalities have been described in post traumatic stress disorder (PTSD), but only a few studies have focused on cortical thickness alterations in recent onset PTSD. In this study, we adopted surface-based morphometry (SBM), which enables an exploration of global structural changes throughout the brain, in order to compare cortical thickness alterations in recent onset PTSD patients, trauma-exposed subjects but without PTSD, and normal controls. Moreover, we used region of interest (ROI) partial correlation analysis to evaluate the correlation among PTSD symptom severity and significant changes of cortical thickness. The widespread cortical thickness reduction relative to the normal controls were found in bilateral inferior and superior parietal lobes, frontal lobes, hippocampus, cingulate cortex, and right lateral occipital lobes in trauma survivors, whereas cortical thickness was only increased in left calcarine cortex in PTSD group. The average cortical thickness of hippocampus and cingulate cortex decreased by 10.75% and 9.09% in PTSD, 3.48% and 2.86% in non PTSD. We further demonstrated that the cortical thicknesses of bilateral ACC and PCC, superior frontal lobes, and hippocampus are negatively correlated with CAPS scores in all trauma survivors. Our study results suggest that stress widens cortical thinning regions and causes more serious effect in recent onset PTSD than non PTSD. It also shows that the cortical thinning in recent onset PTSD predicts the symptom severity. Elsevier 2013-09-03 /pmc/articles/PMC3815016/ /pubmed/24273707 http://dx.doi.org/10.1016/j.nicl.2013.08.013 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Qi, Shun
Mu, Yunfeng
Liu, Kang
Zhang, Jian
Huan, Yi
Tan, Qingrong
Shi, Mei
Wang, Qiang
Chen, Yunchun
Wang, Huaihai
Wang, Huaning
Zhang, Nanyin
Zhang, Xiaoliang
Xiong, Lize
Yin, Hong
Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title_full Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title_fullStr Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title_full_unstemmed Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title_short Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure()
title_sort cortical inhibition deficits in recent onset ptsd after a single prolonged trauma exposure()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815016/
https://www.ncbi.nlm.nih.gov/pubmed/24273707
http://dx.doi.org/10.1016/j.nicl.2013.08.013
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