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Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS

Despite being a popular neuromodulation technique, clinical translation of transcranial direct current stimulation (tDCS) is hampered by variable responses observed within treatment cohorts. Addressing this challenge has been difficult due to the lack of an effective means of mapping the neuromodula...

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Autores principales: Jog, Mayank, Jann, Kay, Yan, Lirong, Huang, Yu, Parra, Lucas, Narr, Katherine, Bikson, Marom, Wang, Danny J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186453/
https://www.ncbi.nlm.nih.gov/pubmed/32372913
http://dx.doi.org/10.3389/fnins.2020.00374
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author Jog, Mayank
Jann, Kay
Yan, Lirong
Huang, Yu
Parra, Lucas
Narr, Katherine
Bikson, Marom
Wang, Danny J. J.
author_facet Jog, Mayank
Jann, Kay
Yan, Lirong
Huang, Yu
Parra, Lucas
Narr, Katherine
Bikson, Marom
Wang, Danny J. J.
author_sort Jog, Mayank
collection PubMed
description Despite being a popular neuromodulation technique, clinical translation of transcranial direct current stimulation (tDCS) is hampered by variable responses observed within treatment cohorts. Addressing this challenge has been difficult due to the lack of an effective means of mapping the neuromodulatory electromagnetic fields together with the brain’s response. In this study, we present a novel imaging technique that provides the capability of concurrently mapping markers of tDCS currents, as well as the brain’s response to tDCS. A dual-echo echo-planar imaging (DE-EPI) sequence is used, wherein the phase of the acquired MRI-signal encodes the tDCS current induced magnetic field, while the magnitude encodes the blood oxygenation level dependent (BOLD) contrast. The proposed technique was first validated in a custom designed phantom. Subsequent test–retest experiments in human participants showed that tDCS-induced magnetic fields can be detected reliably in vivo. The concurrently acquired BOLD data revealed large-scale networks characteristic of a brain in resting-state as well as a ‘cathodal’ and an ‘anodal’ resting-state component under each electrode. Moreover, ‘cathodal’s BOLD-signal was observed to significantly decrease with the applied current at the group level in all datasets. With its ability to image markers of electromagnetic cause as well as neurophysiological changes, the proposed technique may provide an effective means to visualize neural engagement in tDCS at the group level. Our technique also contributes to addressing confounding factors in applying BOLD fMRI concurrently with tDCS.
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spelling pubmed-71864532020-05-05 Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS Jog, Mayank Jann, Kay Yan, Lirong Huang, Yu Parra, Lucas Narr, Katherine Bikson, Marom Wang, Danny J. J. Front Neurosci Neuroscience Despite being a popular neuromodulation technique, clinical translation of transcranial direct current stimulation (tDCS) is hampered by variable responses observed within treatment cohorts. Addressing this challenge has been difficult due to the lack of an effective means of mapping the neuromodulatory electromagnetic fields together with the brain’s response. In this study, we present a novel imaging technique that provides the capability of concurrently mapping markers of tDCS currents, as well as the brain’s response to tDCS. A dual-echo echo-planar imaging (DE-EPI) sequence is used, wherein the phase of the acquired MRI-signal encodes the tDCS current induced magnetic field, while the magnitude encodes the blood oxygenation level dependent (BOLD) contrast. The proposed technique was first validated in a custom designed phantom. Subsequent test–retest experiments in human participants showed that tDCS-induced magnetic fields can be detected reliably in vivo. The concurrently acquired BOLD data revealed large-scale networks characteristic of a brain in resting-state as well as a ‘cathodal’ and an ‘anodal’ resting-state component under each electrode. Moreover, ‘cathodal’s BOLD-signal was observed to significantly decrease with the applied current at the group level in all datasets. With its ability to image markers of electromagnetic cause as well as neurophysiological changes, the proposed technique may provide an effective means to visualize neural engagement in tDCS at the group level. Our technique also contributes to addressing confounding factors in applying BOLD fMRI concurrently with tDCS. Frontiers Media S.A. 2020-04-21 /pmc/articles/PMC7186453/ /pubmed/32372913 http://dx.doi.org/10.3389/fnins.2020.00374 Text en Copyright © 2020 Jog, Jann, Yan, Huang, Parra, Narr, Bikson and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Jog, Mayank
Jann, Kay
Yan, Lirong
Huang, Yu
Parra, Lucas
Narr, Katherine
Bikson, Marom
Wang, Danny J. J.
Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title_full Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title_fullStr Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title_full_unstemmed Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title_short Concurrent Imaging of Markers of Current Flow and Neurophysiological Changes During tDCS
title_sort concurrent imaging of markers of current flow and neurophysiological changes during tdcs
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186453/
https://www.ncbi.nlm.nih.gov/pubmed/32372913
http://dx.doi.org/10.3389/fnins.2020.00374
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