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Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression

BACKGROUND: The efficacy of repetitive transcranial magnetic stimulation (rTMS) to the left dorsolateral prefrontal cortex (dlPFC) has been established in patients with treatment-resistant depression (TRD), suggesting that alterations in signal propagation from the left dlPFC to other brain regions...

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Autores principales: Wada, Masataka, Nakajima, Shinichiro, Honda, Shiori, Takano, Mayuko, Taniguchi, Keita, Tsugawa, Sakiko, Mimura, Yu, Hattori, Nanao, Koike, Shinsuke, Zomorrodi, Reza, Blumberger, Daniel M., Daskalakis, Zafiris J., Mimura, Masaru, Noda, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Impact Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484613/
https://www.ncbi.nlm.nih.gov/pubmed/36104082
http://dx.doi.org/10.1503/jpn.220102
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author Wada, Masataka
Nakajima, Shinichiro
Honda, Shiori
Takano, Mayuko
Taniguchi, Keita
Tsugawa, Sakiko
Mimura, Yu
Hattori, Nanao
Koike, Shinsuke
Zomorrodi, Reza
Blumberger, Daniel M.
Daskalakis, Zafiris J.
Mimura, Masaru
Noda, Yoshihiro
author_facet Wada, Masataka
Nakajima, Shinichiro
Honda, Shiori
Takano, Mayuko
Taniguchi, Keita
Tsugawa, Sakiko
Mimura, Yu
Hattori, Nanao
Koike, Shinsuke
Zomorrodi, Reza
Blumberger, Daniel M.
Daskalakis, Zafiris J.
Mimura, Masaru
Noda, Yoshihiro
author_sort Wada, Masataka
collection PubMed
description BACKGROUND: The efficacy of repetitive transcranial magnetic stimulation (rTMS) to the left dorsolateral prefrontal cortex (dlPFC) has been established in patients with treatment-resistant depression (TRD), suggesting that alterations in signal propagation from the left dlPFC to other brain regions may be linked to the pathophysiology of TRD. Alterations at the cellular level, including dysfunction of oligodendrocytes, may contribute to these network abnormalities. The objectives of the present study were to compare signal propagation from the left dlPFC to other neural networks in patients with TRD and healthy controls. We used TMS combined with electroencephalography to explore links between cell-specific gene expression and signal propagation in TRD using a virtual-histology approach. METHODS: We examined source-level estimated signal propagation from the left dlPFC to the 7 neural networks in 60 patients with TRD and 30 healthy controls. We also calculated correlations between the interregional profiles of altered signal propagation and gene expression for 9 neural cell types derived from the Allen Human Brain Atlas data set. RESULTS: Signal propagation from the left dlPFC to the salience network was reduced in the θ and α bands in patients with TRD (p = 0.0055). Furthermore, this decreased signal propagation was correlated with cellspecific gene expression of oligodendrocytes (p < 0.000001). LIMITATIONS: These results show only part of the pathophysiology of TRD, because stimulation was limited to the left dlPFC. CONCLUSION: Reduced signal propagation from the left dlPFC to the salience network may represent a pathophysiological endophenotype of TRD; this finding may be associated with reduced expression of oligodendrocytes.
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spelling pubmed-94846132022-09-23 Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression Wada, Masataka Nakajima, Shinichiro Honda, Shiori Takano, Mayuko Taniguchi, Keita Tsugawa, Sakiko Mimura, Yu Hattori, Nanao Koike, Shinsuke Zomorrodi, Reza Blumberger, Daniel M. Daskalakis, Zafiris J. Mimura, Masaru Noda, Yoshihiro J Psychiatry Neurosci Research Paper BACKGROUND: The efficacy of repetitive transcranial magnetic stimulation (rTMS) to the left dorsolateral prefrontal cortex (dlPFC) has been established in patients with treatment-resistant depression (TRD), suggesting that alterations in signal propagation from the left dlPFC to other brain regions may be linked to the pathophysiology of TRD. Alterations at the cellular level, including dysfunction of oligodendrocytes, may contribute to these network abnormalities. The objectives of the present study were to compare signal propagation from the left dlPFC to other neural networks in patients with TRD and healthy controls. We used TMS combined with electroencephalography to explore links between cell-specific gene expression and signal propagation in TRD using a virtual-histology approach. METHODS: We examined source-level estimated signal propagation from the left dlPFC to the 7 neural networks in 60 patients with TRD and 30 healthy controls. We also calculated correlations between the interregional profiles of altered signal propagation and gene expression for 9 neural cell types derived from the Allen Human Brain Atlas data set. RESULTS: Signal propagation from the left dlPFC to the salience network was reduced in the θ and α bands in patients with TRD (p = 0.0055). Furthermore, this decreased signal propagation was correlated with cellspecific gene expression of oligodendrocytes (p < 0.000001). LIMITATIONS: These results show only part of the pathophysiology of TRD, because stimulation was limited to the left dlPFC. CONCLUSION: Reduced signal propagation from the left dlPFC to the salience network may represent a pathophysiological endophenotype of TRD; this finding may be associated with reduced expression of oligodendrocytes. CMA Impact Inc. 2022-09-14 /pmc/articles/PMC9484613/ /pubmed/36104082 http://dx.doi.org/10.1503/jpn.220102 Text en © 2022 CMA Impact Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research Paper
Wada, Masataka
Nakajima, Shinichiro
Honda, Shiori
Takano, Mayuko
Taniguchi, Keita
Tsugawa, Sakiko
Mimura, Yu
Hattori, Nanao
Koike, Shinsuke
Zomorrodi, Reza
Blumberger, Daniel M.
Daskalakis, Zafiris J.
Mimura, Masaru
Noda, Yoshihiro
Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title_full Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title_fullStr Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title_full_unstemmed Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title_short Reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
title_sort reduced signal propagation elicited by frontal transcranial magnetic stimulation is associated with oligodendrocyte abnormalities in treatment-resistant depression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484613/
https://www.ncbi.nlm.nih.gov/pubmed/36104082
http://dx.doi.org/10.1503/jpn.220102
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