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Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma

BACKGROUND: There is a significant number of military personnel with a history of mild traumatic brain injury (mTBI) who suffer from comorbid posttraumatic stress symptoms (PTS). Although there is evidence of disruptions of the default mode network (DMN) associated with PTS and mTBI, previous studie...

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Autores principales: Dretsch, Michael N, Rangaprakash, D, Katz, Jeffrey S, Daniel, Thomas A, Goodman, Adam M, Denney, Thomas S, Deshpande, Gopikrishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423682/
https://www.ncbi.nlm.nih.gov/pubmed/30911222
http://dx.doi.org/10.1177/1179069519833966
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author Dretsch, Michael N
Rangaprakash, D
Katz, Jeffrey S
Daniel, Thomas A
Goodman, Adam M
Denney, Thomas S
Deshpande, Gopikrishna
author_facet Dretsch, Michael N
Rangaprakash, D
Katz, Jeffrey S
Daniel, Thomas A
Goodman, Adam M
Denney, Thomas S
Deshpande, Gopikrishna
author_sort Dretsch, Michael N
collection PubMed
description BACKGROUND: There is a significant number of military personnel with a history of mild traumatic brain injury (mTBI) who suffer from comorbid posttraumatic stress symptoms (PTS). Although there is evidence of disruptions of the default mode network (DMN) associated with PTS and mTBI, previous studies have only studied static connectivity while ignoring temporal variability of connectivity. OBJECTIVE: To assess DMN disrupted or dysregulated neurocircuitry, cognitive functioning, and psychological health of active-duty military with mTBI and PTS. METHOD: U.S. Army soldiers with PTS (n = 14), mTBI + PTS (n = 25), and healthy controls (n = 21) voluntarily completed a cognitive and symptom battery. In addition, participants had magnetic resonance imaging (MRI) to assess both static functional connectivity (SFC) and variance of dynamic functional connectivity (vDFC) of the DMN. RESULTS: Both the PTS and mTBI + PTS groups had significant symptoms, but only the comorbid group had significant decrements in cognitive functioning. Both groups showed less stable and disrupted neural signatures of the DMN, mainly constituting the cingulate-frontal-temporal-parietal attention network. Specifically, the PTS group showed a combination of both reduced contralateral strength and reduced unilateral variability of frontal-cingulate-temporal connectivities, as well as increased variability of frontal-parietal connectivities. The mTBI + PTS group had fewer abnormal connectives than the PTS group, all of which included reduced strength of frontal-temporal regions and reduced variability frontal-cingulate-temporal regions. Greater SFC and vDFC connectivity of the left dorsolateral prefrontal cortex (dlPFC) ↔ precuneus was associated with higher cognitive scores and lower symptom scores. CONCLUSIONS: Findings suggest that individuals with PTS and mTBI + PTS have a propensity for accentuated generation of thoughts, feelings, sensations, and/or images while in a resting state. Compared with controls, only the PTS group was associated with accentuated variability of the frontal-parietal attention network. While there were no significant differences in DMN connectivity strength between the mTBI + PTS and PTS groups, variability of connectivity was able to distinguish them.
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spelling pubmed-64236822019-03-25 Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma Dretsch, Michael N Rangaprakash, D Katz, Jeffrey S Daniel, Thomas A Goodman, Adam M Denney, Thomas S Deshpande, Gopikrishna J Exp Neurosci Traumatic Brain Injury (TBI) and Chronic Traumatic Encephalopathy (CTE) BACKGROUND: There is a significant number of military personnel with a history of mild traumatic brain injury (mTBI) who suffer from comorbid posttraumatic stress symptoms (PTS). Although there is evidence of disruptions of the default mode network (DMN) associated with PTS and mTBI, previous studies have only studied static connectivity while ignoring temporal variability of connectivity. OBJECTIVE: To assess DMN disrupted or dysregulated neurocircuitry, cognitive functioning, and psychological health of active-duty military with mTBI and PTS. METHOD: U.S. Army soldiers with PTS (n = 14), mTBI + PTS (n = 25), and healthy controls (n = 21) voluntarily completed a cognitive and symptom battery. In addition, participants had magnetic resonance imaging (MRI) to assess both static functional connectivity (SFC) and variance of dynamic functional connectivity (vDFC) of the DMN. RESULTS: Both the PTS and mTBI + PTS groups had significant symptoms, but only the comorbid group had significant decrements in cognitive functioning. Both groups showed less stable and disrupted neural signatures of the DMN, mainly constituting the cingulate-frontal-temporal-parietal attention network. Specifically, the PTS group showed a combination of both reduced contralateral strength and reduced unilateral variability of frontal-cingulate-temporal connectivities, as well as increased variability of frontal-parietal connectivities. The mTBI + PTS group had fewer abnormal connectives than the PTS group, all of which included reduced strength of frontal-temporal regions and reduced variability frontal-cingulate-temporal regions. Greater SFC and vDFC connectivity of the left dorsolateral prefrontal cortex (dlPFC) ↔ precuneus was associated with higher cognitive scores and lower symptom scores. CONCLUSIONS: Findings suggest that individuals with PTS and mTBI + PTS have a propensity for accentuated generation of thoughts, feelings, sensations, and/or images while in a resting state. Compared with controls, only the PTS group was associated with accentuated variability of the frontal-parietal attention network. While there were no significant differences in DMN connectivity strength between the mTBI + PTS and PTS groups, variability of connectivity was able to distinguish them. SAGE Publications 2019-03-18 /pmc/articles/PMC6423682/ /pubmed/30911222 http://dx.doi.org/10.1177/1179069519833966 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Traumatic Brain Injury (TBI) and Chronic Traumatic Encephalopathy (CTE)
Dretsch, Michael N
Rangaprakash, D
Katz, Jeffrey S
Daniel, Thomas A
Goodman, Adam M
Denney, Thomas S
Deshpande, Gopikrishna
Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title_full Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title_fullStr Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title_full_unstemmed Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title_short Strength and Temporal Variance of the Default Mode Network to Investigate Chronic Mild Traumatic Brain Injury in Service Members with Psychological Trauma
title_sort strength and temporal variance of the default mode network to investigate chronic mild traumatic brain injury in service members with psychological trauma
topic Traumatic Brain Injury (TBI) and Chronic Traumatic Encephalopathy (CTE)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423682/
https://www.ncbi.nlm.nih.gov/pubmed/30911222
http://dx.doi.org/10.1177/1179069519833966
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