Cargando…

Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury

OBJECTIVES: Previous studies have established the role of the cortico‐mesolimbic and descending pain modulation systems in chronic pain prediction. Mild traumatic brain injury (mTBI) is an acute pain model where chronic pain is prevalent and complicated for prediction. In this study, we set out to s...

Descripción completa

Detalles Bibliográficos
Autores principales: Bosak, Noam, Branco, Paulo, Kuperman, Pora, Buxbaum, Chen, Cohen, Ruth Manor, Fadel, Shiri, Zubeidat, Rabab, Hadad, Rafi, Lawen, Amir, Saadon‐Grosman, Noam, Sterling, Michele, Granovsky, Yelena, Apkarian, Apkar Vania, Yarnitsky, David, Kahn, Itamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826527/
https://www.ncbi.nlm.nih.gov/pubmed/36082761
http://dx.doi.org/10.1002/ana.26463
_version_ 1784866873353961472
author Bosak, Noam
Branco, Paulo
Kuperman, Pora
Buxbaum, Chen
Cohen, Ruth Manor
Fadel, Shiri
Zubeidat, Rabab
Hadad, Rafi
Lawen, Amir
Saadon‐Grosman, Noam
Sterling, Michele
Granovsky, Yelena
Apkarian, Apkar Vania
Yarnitsky, David
Kahn, Itamar
author_facet Bosak, Noam
Branco, Paulo
Kuperman, Pora
Buxbaum, Chen
Cohen, Ruth Manor
Fadel, Shiri
Zubeidat, Rabab
Hadad, Rafi
Lawen, Amir
Saadon‐Grosman, Noam
Sterling, Michele
Granovsky, Yelena
Apkarian, Apkar Vania
Yarnitsky, David
Kahn, Itamar
author_sort Bosak, Noam
collection PubMed
description OBJECTIVES: Previous studies have established the role of the cortico‐mesolimbic and descending pain modulation systems in chronic pain prediction. Mild traumatic brain injury (mTBI) is an acute pain model where chronic pain is prevalent and complicated for prediction. In this study, we set out to study whether functional connectivity (FC) of the nucleus accumbens (NAc) and the periaqueductal gray matter (PAG) is predictive of pain chronification in early‐acute mTBI. METHODS: To estimate FC, resting‐state functional magnetic resonance imaging (fMRI) of 105 participants with mTBI following a motor vehicle collision was acquired within 72 hours post‐accident. Participants were classified according to pain ratings provided at 12‐months post‐collision into chronic pain (head/neck pain ≥30/100, n = 44) and recovery (n = 61) groups, and their FC maps were compared. RESULTS: The chronic pain group exhibited reduced negative FC between NAc and a region within the primary motor cortex corresponding with the expected representation of the area of injury. A complementary pattern was also demonstrated between PAG and the primary somatosensory cortex. PAG and NAc also shared increased FC to the rostral anterior cingulate cortex (rACC) within the recovery group. Brain connectivity further shows high classification accuracy (area under the curve [AUC] = .86) for future chronic pain, when combined with an acute pain intensity report. INTERPRETATION: FC features obtained shortly after mTBI predict its transition to long‐term chronic pain, and may reflect an underlying interaction of injury‐related primary sensorimotor cortical areas with the mesolimbic and pain modulation systems. Our findings indicate a potential predictive biomarker and highlight targets for future early preventive interventions. ANN NEUROL 2022;92:819–833
format Online
Article
Text
id pubmed-9826527
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-98265272023-01-09 Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury Bosak, Noam Branco, Paulo Kuperman, Pora Buxbaum, Chen Cohen, Ruth Manor Fadel, Shiri Zubeidat, Rabab Hadad, Rafi Lawen, Amir Saadon‐Grosman, Noam Sterling, Michele Granovsky, Yelena Apkarian, Apkar Vania Yarnitsky, David Kahn, Itamar Ann Neurol Research Articles OBJECTIVES: Previous studies have established the role of the cortico‐mesolimbic and descending pain modulation systems in chronic pain prediction. Mild traumatic brain injury (mTBI) is an acute pain model where chronic pain is prevalent and complicated for prediction. In this study, we set out to study whether functional connectivity (FC) of the nucleus accumbens (NAc) and the periaqueductal gray matter (PAG) is predictive of pain chronification in early‐acute mTBI. METHODS: To estimate FC, resting‐state functional magnetic resonance imaging (fMRI) of 105 participants with mTBI following a motor vehicle collision was acquired within 72 hours post‐accident. Participants were classified according to pain ratings provided at 12‐months post‐collision into chronic pain (head/neck pain ≥30/100, n = 44) and recovery (n = 61) groups, and their FC maps were compared. RESULTS: The chronic pain group exhibited reduced negative FC between NAc and a region within the primary motor cortex corresponding with the expected representation of the area of injury. A complementary pattern was also demonstrated between PAG and the primary somatosensory cortex. PAG and NAc also shared increased FC to the rostral anterior cingulate cortex (rACC) within the recovery group. Brain connectivity further shows high classification accuracy (area under the curve [AUC] = .86) for future chronic pain, when combined with an acute pain intensity report. INTERPRETATION: FC features obtained shortly after mTBI predict its transition to long‐term chronic pain, and may reflect an underlying interaction of injury‐related primary sensorimotor cortical areas with the mesolimbic and pain modulation systems. Our findings indicate a potential predictive biomarker and highlight targets for future early preventive interventions. ANN NEUROL 2022;92:819–833 John Wiley & Sons, Inc. 2022-09-09 2022-11 /pmc/articles/PMC9826527/ /pubmed/36082761 http://dx.doi.org/10.1002/ana.26463 Text en © 2022 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Bosak, Noam
Branco, Paulo
Kuperman, Pora
Buxbaum, Chen
Cohen, Ruth Manor
Fadel, Shiri
Zubeidat, Rabab
Hadad, Rafi
Lawen, Amir
Saadon‐Grosman, Noam
Sterling, Michele
Granovsky, Yelena
Apkarian, Apkar Vania
Yarnitsky, David
Kahn, Itamar
Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title_full Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title_fullStr Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title_full_unstemmed Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title_short Brain Connectivity Predicts Chronic Pain in Acute Mild Traumatic Brain Injury
title_sort brain connectivity predicts chronic pain in acute mild traumatic brain injury
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826527/
https://www.ncbi.nlm.nih.gov/pubmed/36082761
http://dx.doi.org/10.1002/ana.26463
work_keys_str_mv AT bosaknoam brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT brancopaulo brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT kupermanpora brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT buxbaumchen brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT cohenruthmanor brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT fadelshiri brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT zubeidatrabab brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT hadadrafi brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT lawenamir brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT saadongrosmannoam brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT sterlingmichele brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT granovskyyelena brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT apkarianapkarvania brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT yarnitskydavid brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury
AT kahnitamar brainconnectivitypredictschronicpaininacutemildtraumaticbraininjury