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Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia
Background: The neural basis of treatment-resistant schizophrenia (TRS) remains unclear. Previous neuroimaging studies suggest that aberrant connectivity between the anterior cingulate cortex (ACC) and default mode network (DMN) may play a key role in the pathophysiology of TRS. Thus, we aimed to ex...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564631/ https://www.ncbi.nlm.nih.gov/pubmed/32823914 http://dx.doi.org/10.3390/jpm10030089 |
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author | Wada, Masataka Nakajima, Shinichiro Tarumi, Ryosuke Masuda, Fumi Miyazaki, Takahiro Tsugawa, Sakiko Ogyu, Kamiyu Honda, Shiori Matsushita, Karin Kikuchi, Yudai Fujii, Shinya Blumberger, Daniel M. Daskalakis, Zafiris J. Mimura, Masaru Noda, Yoshihiro |
author_facet | Wada, Masataka Nakajima, Shinichiro Tarumi, Ryosuke Masuda, Fumi Miyazaki, Takahiro Tsugawa, Sakiko Ogyu, Kamiyu Honda, Shiori Matsushita, Karin Kikuchi, Yudai Fujii, Shinya Blumberger, Daniel M. Daskalakis, Zafiris J. Mimura, Masaru Noda, Yoshihiro |
author_sort | Wada, Masataka |
collection | PubMed |
description | Background: The neural basis of treatment-resistant schizophrenia (TRS) remains unclear. Previous neuroimaging studies suggest that aberrant connectivity between the anterior cingulate cortex (ACC) and default mode network (DMN) may play a key role in the pathophysiology of TRS. Thus, we aimed to examine the connectivity between the ACC and posterior cingulate cortex (PCC), a hub of the DMN, computing isolated effective coherence (iCoh), which represents causal effective connectivity. Methods: Resting-state electroencephalogram with 19 channels was acquired from seventeen patients with TRS and thirty patients with non-TRS (nTRS). The iCoh values between the PCC and ACC were calculated using sLORETA software. We conducted four-way analyses of variance (ANOVAs) for iCoh values with group as a between-subject factor and frequency, directionality, and laterality as within-subject factors and post-hoc independent t-tests. Results: The ANOVA and post-hoc t-tests for the iCoh ratio of directionality from PCC to ACC showed significant findings in delta (t(45) = 7.659, p = 0.008) and theta (t(45) = 8.066, p = 0.007) bands in the left side (TRS < nTRS). Conclusion: Left delta and theta PCC and ACC iCoh ratio may represent a neurophysiological basis of TRS. Given the preliminary nature of this study, these results warrant further study to confirm the importance of iCoh as a clinical indicator for treatment-resistance. |
format | Online Article Text |
id | pubmed-7564631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75646312020-10-29 Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia Wada, Masataka Nakajima, Shinichiro Tarumi, Ryosuke Masuda, Fumi Miyazaki, Takahiro Tsugawa, Sakiko Ogyu, Kamiyu Honda, Shiori Matsushita, Karin Kikuchi, Yudai Fujii, Shinya Blumberger, Daniel M. Daskalakis, Zafiris J. Mimura, Masaru Noda, Yoshihiro J Pers Med Article Background: The neural basis of treatment-resistant schizophrenia (TRS) remains unclear. Previous neuroimaging studies suggest that aberrant connectivity between the anterior cingulate cortex (ACC) and default mode network (DMN) may play a key role in the pathophysiology of TRS. Thus, we aimed to examine the connectivity between the ACC and posterior cingulate cortex (PCC), a hub of the DMN, computing isolated effective coherence (iCoh), which represents causal effective connectivity. Methods: Resting-state electroencephalogram with 19 channels was acquired from seventeen patients with TRS and thirty patients with non-TRS (nTRS). The iCoh values between the PCC and ACC were calculated using sLORETA software. We conducted four-way analyses of variance (ANOVAs) for iCoh values with group as a between-subject factor and frequency, directionality, and laterality as within-subject factors and post-hoc independent t-tests. Results: The ANOVA and post-hoc t-tests for the iCoh ratio of directionality from PCC to ACC showed significant findings in delta (t(45) = 7.659, p = 0.008) and theta (t(45) = 8.066, p = 0.007) bands in the left side (TRS < nTRS). Conclusion: Left delta and theta PCC and ACC iCoh ratio may represent a neurophysiological basis of TRS. Given the preliminary nature of this study, these results warrant further study to confirm the importance of iCoh as a clinical indicator for treatment-resistance. MDPI 2020-08-14 /pmc/articles/PMC7564631/ /pubmed/32823914 http://dx.doi.org/10.3390/jpm10030089 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wada, Masataka Nakajima, Shinichiro Tarumi, Ryosuke Masuda, Fumi Miyazaki, Takahiro Tsugawa, Sakiko Ogyu, Kamiyu Honda, Shiori Matsushita, Karin Kikuchi, Yudai Fujii, Shinya Blumberger, Daniel M. Daskalakis, Zafiris J. Mimura, Masaru Noda, Yoshihiro Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title | Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title_full | Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title_fullStr | Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title_full_unstemmed | Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title_short | Resting-State Isolated Effective Connectivity of the Cingulate Cortex as a Neurophysiological Biomarker in Patients with Severe Treatment-Resistant Schizophrenia |
title_sort | resting-state isolated effective connectivity of the cingulate cortex as a neurophysiological biomarker in patients with severe treatment-resistant schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564631/ https://www.ncbi.nlm.nih.gov/pubmed/32823914 http://dx.doi.org/10.3390/jpm10030089 |
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