Cargando…

Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD

Post-traumatic stress disorder (PTSD) is a leading cause of sustained impairment, distress, and poor quality of life in military personnel, veterans, and civilians. Indirect functional neuroimaging studies using PET or fMRI with fear-related stimuli support a PTSD neurocircuitry model that includes...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Ming-Xiong, Yurgil, Kate A., Robb, Ashley, Angeles, Annemarie, Diwakar, Mithun, Risbrough, Victoria B., Nichols, Sharon L., McLay, Robert, Theilmann, Rebecca J., Song, Tao, Huang, Charles W., Lee, Roland R., Baker, Dewleen G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145534/
https://www.ncbi.nlm.nih.gov/pubmed/25180160
http://dx.doi.org/10.1016/j.nicl.2014.08.004
_version_ 1782332198717751296
author Huang, Ming-Xiong
Yurgil, Kate A.
Robb, Ashley
Angeles, Annemarie
Diwakar, Mithun
Risbrough, Victoria B.
Nichols, Sharon L.
McLay, Robert
Theilmann, Rebecca J.
Song, Tao
Huang, Charles W.
Lee, Roland R.
Baker, Dewleen G.
author_facet Huang, Ming-Xiong
Yurgil, Kate A.
Robb, Ashley
Angeles, Annemarie
Diwakar, Mithun
Risbrough, Victoria B.
Nichols, Sharon L.
McLay, Robert
Theilmann, Rebecca J.
Song, Tao
Huang, Charles W.
Lee, Roland R.
Baker, Dewleen G.
author_sort Huang, Ming-Xiong
collection PubMed
description Post-traumatic stress disorder (PTSD) is a leading cause of sustained impairment, distress, and poor quality of life in military personnel, veterans, and civilians. Indirect functional neuroimaging studies using PET or fMRI with fear-related stimuli support a PTSD neurocircuitry model that includes amygdala, hippocampus, and ventromedial prefrontal cortex (vmPFC). However, it is not clear if this model can fully account for PTSD abnormalities detected directly by electromagnetic-based source imaging techniques in resting-state. The present study examined resting-state magnetoencephalography (MEG) signals in 25 active-duty service members and veterans with PTSD and 30 healthy volunteers. In contrast to the healthy volunteers, individuals with PTSD showed: 1) hyperactivity from amygdala, hippocampus, posterolateral orbitofrontal cortex (OFC), dorsomedial prefrontal cortex (dmPFC), and insular cortex in high-frequency (i.e., beta, gamma, and high-gamma) bands; 2) hypoactivity from vmPFC, Frontal Pole (FP), and dorsolateral prefrontal cortex (dlPFC) in high-frequency bands; 3) extensive hypoactivity from dlPFC, FP, anterior temporal lobes, precuneous cortex, and sensorimotor cortex in alpha and low-frequency bands; and 4) in individuals with PTSD, MEG activity in the left amygdala and posterolateral OFC correlated positively with PTSD symptom scores, whereas MEG activity in vmPFC and precuneous correlated negatively with symptom score. The present study showed that MEG source imaging technique revealed new abnormalities in the resting-state electromagnetic signals from the PTSD neurocircuitry. Particularly, posterolateral OFC and precuneous may play important roles in the PTSD neurocircuitry model.
format Online
Article
Text
id pubmed-4145534
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-41455342014-09-01 Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD Huang, Ming-Xiong Yurgil, Kate A. Robb, Ashley Angeles, Annemarie Diwakar, Mithun Risbrough, Victoria B. Nichols, Sharon L. McLay, Robert Theilmann, Rebecca J. Song, Tao Huang, Charles W. Lee, Roland R. Baker, Dewleen G. Neuroimage Clin Regular Articles Post-traumatic stress disorder (PTSD) is a leading cause of sustained impairment, distress, and poor quality of life in military personnel, veterans, and civilians. Indirect functional neuroimaging studies using PET or fMRI with fear-related stimuli support a PTSD neurocircuitry model that includes amygdala, hippocampus, and ventromedial prefrontal cortex (vmPFC). However, it is not clear if this model can fully account for PTSD abnormalities detected directly by electromagnetic-based source imaging techniques in resting-state. The present study examined resting-state magnetoencephalography (MEG) signals in 25 active-duty service members and veterans with PTSD and 30 healthy volunteers. In contrast to the healthy volunteers, individuals with PTSD showed: 1) hyperactivity from amygdala, hippocampus, posterolateral orbitofrontal cortex (OFC), dorsomedial prefrontal cortex (dmPFC), and insular cortex in high-frequency (i.e., beta, gamma, and high-gamma) bands; 2) hypoactivity from vmPFC, Frontal Pole (FP), and dorsolateral prefrontal cortex (dlPFC) in high-frequency bands; 3) extensive hypoactivity from dlPFC, FP, anterior temporal lobes, precuneous cortex, and sensorimotor cortex in alpha and low-frequency bands; and 4) in individuals with PTSD, MEG activity in the left amygdala and posterolateral OFC correlated positively with PTSD symptom scores, whereas MEG activity in vmPFC and precuneous correlated negatively with symptom score. The present study showed that MEG source imaging technique revealed new abnormalities in the resting-state electromagnetic signals from the PTSD neurocircuitry. Particularly, posterolateral OFC and precuneous may play important roles in the PTSD neurocircuitry model. Elsevier 2014-08-07 /pmc/articles/PMC4145534/ /pubmed/25180160 http://dx.doi.org/10.1016/j.nicl.2014.08.004 Text en http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Regular Articles
Huang, Ming-Xiong
Yurgil, Kate A.
Robb, Ashley
Angeles, Annemarie
Diwakar, Mithun
Risbrough, Victoria B.
Nichols, Sharon L.
McLay, Robert
Theilmann, Rebecca J.
Song, Tao
Huang, Charles W.
Lee, Roland R.
Baker, Dewleen G.
Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title_full Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title_fullStr Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title_full_unstemmed Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title_short Voxel-wise resting-state MEG source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with PTSD
title_sort voxel-wise resting-state meg source magnitude imaging study reveals neurocircuitry abnormality in active-duty service members and veterans with ptsd
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145534/
https://www.ncbi.nlm.nih.gov/pubmed/25180160
http://dx.doi.org/10.1016/j.nicl.2014.08.004
work_keys_str_mv AT huangmingxiong voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT yurgilkatea voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT robbashley voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT angelesannemarie voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT diwakarmithun voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT risbroughvictoriab voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT nicholssharonl voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT mclayrobert voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT theilmannrebeccaj voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT songtao voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT huangcharlesw voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT leerolandr voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd
AT bakerdewleeng voxelwiserestingstatemegsourcemagnitudeimagingstudyrevealsneurocircuitryabnormalityinactivedutyservicemembersandveteranswithptsd