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A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder

Post‐traumatic stress disorder (PTSD) and mild traumatic brain injury (mTBI) often co‐occur in the context of threat to one's life. These conditions also have an overlapping symptomatology and include symptoms of anxiety, poor concentration and memory problems. A major challenge has been articu...

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Autores principales: Klimova, Aleksandra, Breukelaar, Isabella A., Bryant, Richard A., Korgaonkar, Mayuresh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842915/
https://www.ncbi.nlm.nih.gov/pubmed/36206284
http://dx.doi.org/10.1002/hbm.26101
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author Klimova, Aleksandra
Breukelaar, Isabella A.
Bryant, Richard A.
Korgaonkar, Mayuresh S.
author_facet Klimova, Aleksandra
Breukelaar, Isabella A.
Bryant, Richard A.
Korgaonkar, Mayuresh S.
author_sort Klimova, Aleksandra
collection PubMed
description Post‐traumatic stress disorder (PTSD) and mild traumatic brain injury (mTBI) often co‐occur in the context of threat to one's life. These conditions also have an overlapping symptomatology and include symptoms of anxiety, poor concentration and memory problems. A major challenge has been articulating the underlying neurobiology of these overlapping conditions. The primary aim of this study was to compare intrinsic functional connectivity between mTBI (without PTSD) and PTSD (without mTBI). The study included functional MRI data from 176 participants: 42 participants with mTBI, 67 with PTSD and a comparison group of 66 age and sex‐matched healthy controls. We used network‐based statistical analyses for connectome‐wide comparisons of intrinsic functional connectivity between mTBI relative to PTSD and controls. Our results showed no connectivity differences between mTBI and PTSD groups. However, we did find that mTBI had significantly reduced connectivity relative to healthy controls within an extensive network of regions including default mode, executive control, visual and auditory networks. The mTBI group also displayed hyperconnectivity between dorsal and ventral attention networks and perceptual regions. The PTSD group also demonstrated abnormal connectivity within these networks relative to controls. Connectivity alterations were not associated with severity of PTSD or post‐concussive symptoms in either clinical group. Taken together, the similar profiles of intrinsic connectivity alterations in these two conditions provide neural evidence that can explain, in part, the overlapping symptomatology between mTBI and PTSD.
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spelling pubmed-98429152023-01-23 A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder Klimova, Aleksandra Breukelaar, Isabella A. Bryant, Richard A. Korgaonkar, Mayuresh S. Hum Brain Mapp Research Articles Post‐traumatic stress disorder (PTSD) and mild traumatic brain injury (mTBI) often co‐occur in the context of threat to one's life. These conditions also have an overlapping symptomatology and include symptoms of anxiety, poor concentration and memory problems. A major challenge has been articulating the underlying neurobiology of these overlapping conditions. The primary aim of this study was to compare intrinsic functional connectivity between mTBI (without PTSD) and PTSD (without mTBI). The study included functional MRI data from 176 participants: 42 participants with mTBI, 67 with PTSD and a comparison group of 66 age and sex‐matched healthy controls. We used network‐based statistical analyses for connectome‐wide comparisons of intrinsic functional connectivity between mTBI relative to PTSD and controls. Our results showed no connectivity differences between mTBI and PTSD groups. However, we did find that mTBI had significantly reduced connectivity relative to healthy controls within an extensive network of regions including default mode, executive control, visual and auditory networks. The mTBI group also displayed hyperconnectivity between dorsal and ventral attention networks and perceptual regions. The PTSD group also demonstrated abnormal connectivity within these networks relative to controls. Connectivity alterations were not associated with severity of PTSD or post‐concussive symptoms in either clinical group. Taken together, the similar profiles of intrinsic connectivity alterations in these two conditions provide neural evidence that can explain, in part, the overlapping symptomatology between mTBI and PTSD. John Wiley & Sons, Inc. 2022-10-07 /pmc/articles/PMC9842915/ /pubmed/36206284 http://dx.doi.org/10.1002/hbm.26101 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Klimova, Aleksandra
Breukelaar, Isabella A.
Bryant, Richard A.
Korgaonkar, Mayuresh S.
A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title_full A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title_fullStr A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title_full_unstemmed A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title_short A comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
title_sort comparison of the functional connectome in mild traumatic brain injury and post‐traumatic stress disorder
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842915/
https://www.ncbi.nlm.nih.gov/pubmed/36206284
http://dx.doi.org/10.1002/hbm.26101
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