Cargando…

Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury

Increased task-related blood oxygen level dependent (BOLD) activation is commonly observed in functional magnetic resonance imaging (fMRI) studies of moderate/severe traumatic brain injury (msTBI), but the functional relevance of these hyperactivations and how they are linked to more direct measures...

Descripción completa

Detalles Bibliográficos
Autores principales: Olsen, Alexander, Babikian, Talin, Dennis, Emily L., Ellis-Blied, Monica U., Giza, Christopher, Marion, Sarah DeBoard, Mink, Richard, Johnson, Jeffrey, Babbitt, Christopher J., Thompson, Paul M., Asarnow, Robert F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964811/
https://www.ncbi.nlm.nih.gov/pubmed/31469049
http://dx.doi.org/10.1089/neu.2019.6532
_version_ 1783488524353273856
author Olsen, Alexander
Babikian, Talin
Dennis, Emily L.
Ellis-Blied, Monica U.
Giza, Christopher
Marion, Sarah DeBoard
Mink, Richard
Johnson, Jeffrey
Babbitt, Christopher J.
Thompson, Paul M.
Asarnow, Robert F.
author_facet Olsen, Alexander
Babikian, Talin
Dennis, Emily L.
Ellis-Blied, Monica U.
Giza, Christopher
Marion, Sarah DeBoard
Mink, Richard
Johnson, Jeffrey
Babbitt, Christopher J.
Thompson, Paul M.
Asarnow, Robert F.
author_sort Olsen, Alexander
collection PubMed
description Increased task-related blood oxygen level dependent (BOLD) activation is commonly observed in functional magnetic resonance imaging (fMRI) studies of moderate/severe traumatic brain injury (msTBI), but the functional relevance of these hyperactivations and how they are linked to more direct measures of neuronal function remain largely unknown. Here, we investigated how working memory load (WML)-dependent BOLD activation was related to an electrophysiological measure of interhemispheric transfer time (IHTT) in a sample of 18 msTBI patients and 26 demographically matched controls from the UCLA RAPBI (Recovery after Pediatric Brain Injury) study. In the context of highly similar fMRI task performance, a subgroup of TBI patients with slow IHTT had greater BOLD activation with higher WML than both healthy control children and a subgroup of msTBI patients with normal IHTT. Slower IHTT treated as a continuous variable was also associated with BOLD hyperactivation in the full TBI sample and in controls. Higher WML-dependent BOLD activation was related to better performance on a clinical cognitive performance index, an association that was more pronounced within the patient group with slow IHTT. Our previous work has shown that a subgroup of children with slow IHTT after pediatric msTBI has increased risk for poor white matter organization, long-term neurodegeneration, and poor cognitive outcome. BOLD hyperactivations after msTBI may reflect neuronal compensatory processes supporting higher-order capacity demanding cognitive functions in the context of inefficient neuronal transfer of information. The link between BOLD hyperactivations and slow IHTT adds to the multi-modal validation of this electrophysiological measure as a promising biomarker.
format Online
Article
Text
id pubmed-6964811
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Mary Ann Liebert, Inc., publishers
record_format MEDLINE/PubMed
spelling pubmed-69648112020-02-10 Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury Olsen, Alexander Babikian, Talin Dennis, Emily L. Ellis-Blied, Monica U. Giza, Christopher Marion, Sarah DeBoard Mink, Richard Johnson, Jeffrey Babbitt, Christopher J. Thompson, Paul M. Asarnow, Robert F. J Neurotrauma Original Articles Increased task-related blood oxygen level dependent (BOLD) activation is commonly observed in functional magnetic resonance imaging (fMRI) studies of moderate/severe traumatic brain injury (msTBI), but the functional relevance of these hyperactivations and how they are linked to more direct measures of neuronal function remain largely unknown. Here, we investigated how working memory load (WML)-dependent BOLD activation was related to an electrophysiological measure of interhemispheric transfer time (IHTT) in a sample of 18 msTBI patients and 26 demographically matched controls from the UCLA RAPBI (Recovery after Pediatric Brain Injury) study. In the context of highly similar fMRI task performance, a subgroup of TBI patients with slow IHTT had greater BOLD activation with higher WML than both healthy control children and a subgroup of msTBI patients with normal IHTT. Slower IHTT treated as a continuous variable was also associated with BOLD hyperactivation in the full TBI sample and in controls. Higher WML-dependent BOLD activation was related to better performance on a clinical cognitive performance index, an association that was more pronounced within the patient group with slow IHTT. Our previous work has shown that a subgroup of children with slow IHTT after pediatric msTBI has increased risk for poor white matter organization, long-term neurodegeneration, and poor cognitive outcome. BOLD hyperactivations after msTBI may reflect neuronal compensatory processes supporting higher-order capacity demanding cognitive functions in the context of inefficient neuronal transfer of information. The link between BOLD hyperactivations and slow IHTT adds to the multi-modal validation of this electrophysiological measure as a promising biomarker. Mary Ann Liebert, Inc., publishers 2020-01-15 2019-12-20 /pmc/articles/PMC6964811/ /pubmed/31469049 http://dx.doi.org/10.1089/neu.2019.6532 Text en © Alexander Olsen et al., 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Original Articles
Olsen, Alexander
Babikian, Talin
Dennis, Emily L.
Ellis-Blied, Monica U.
Giza, Christopher
Marion, Sarah DeBoard
Mink, Richard
Johnson, Jeffrey
Babbitt, Christopher J.
Thompson, Paul M.
Asarnow, Robert F.
Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title_full Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title_fullStr Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title_full_unstemmed Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title_short Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury
title_sort functional brain hyperactivations are linked to an electrophysiological measure of slow interhemispheric transfer time after pediatric moderate/severe traumatic brain injury
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964811/
https://www.ncbi.nlm.nih.gov/pubmed/31469049
http://dx.doi.org/10.1089/neu.2019.6532
work_keys_str_mv AT olsenalexander functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT babikiantalin functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT dennisemilyl functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT ellisbliedmonicau functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT gizachristopher functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT marionsarahdeboard functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT minkrichard functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT johnsonjeffrey functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT babbittchristopherj functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT thompsonpaulm functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury
AT asarnowrobertf functionalbrainhyperactivationsarelinkedtoanelectrophysiologicalmeasureofslowinterhemispherictransfertimeafterpediatricmoderateseveretraumaticbraininjury