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Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder

Previous studies suggest that in people with major depressive disorder (MDD), there exists a perturbation of the normal balance between the excitatory and inhibitory neurotransmitter systems in the visual cortex, indicating the possibility of altered visual cortical excitability. However, investigat...

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Autores principales: Du, Hongheng, Shen, Xue, Du, Xiaoyan, Zhao, Libo, Zhou, Wenjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936091/
https://www.ncbi.nlm.nih.gov/pubmed/35321224
http://dx.doi.org/10.3389/fpsyt.2022.844434
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author Du, Hongheng
Shen, Xue
Du, Xiaoyan
Zhao, Libo
Zhou, Wenjun
author_facet Du, Hongheng
Shen, Xue
Du, Xiaoyan
Zhao, Libo
Zhou, Wenjun
author_sort Du, Hongheng
collection PubMed
description Previous studies suggest that in people with major depressive disorder (MDD), there exists a perturbation of the normal balance between the excitatory and inhibitory neurotransmitter systems in the visual cortex, indicating the possibility of altered visual cortical excitability. However, investigations into the neural activities of the visual cortex in MDD patients yielded inconsistent findings. The present study aimed to evaluate the visual cortical excitability utilizing a paired-pulse stimulation paradigm in patients with MDD and to access the paired-pulse behavior of recording visual evoked potentials (VEPs) as a marker of MDD. We analyzed the amplitudes of VEPs and paired-pulse suppression (PPS) at four different stimulus onset asynchronies (SOAs) spanning 93 ms to 133 ms. Further, the relationship between PPS and the symptom severity of depression was investigated using Spearman's correlation. We found that, whereas the first VEP amplitude remained unchanged, the second VEP amplitude was significantly higher in the MDD group compared to the healthy controls. As a result, the amplitude ratio (second VEP amplitude/first VEP amplitude) increased, indicating reduced PPS and thus increased excitability in the visual cortex. Moreover, we found the amplitude ratios had a significantly positive correlation with the symptom severity of depression in MDD, indicating a clinically useful biomarker for MDD. Our findings provide new insights into the changes in the excitation-inhibition balance of visual cortex in MDD, which could pave the way for specific clinical interventions.
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spelling pubmed-89360912022-03-22 Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder Du, Hongheng Shen, Xue Du, Xiaoyan Zhao, Libo Zhou, Wenjun Front Psychiatry Psychiatry Previous studies suggest that in people with major depressive disorder (MDD), there exists a perturbation of the normal balance between the excitatory and inhibitory neurotransmitter systems in the visual cortex, indicating the possibility of altered visual cortical excitability. However, investigations into the neural activities of the visual cortex in MDD patients yielded inconsistent findings. The present study aimed to evaluate the visual cortical excitability utilizing a paired-pulse stimulation paradigm in patients with MDD and to access the paired-pulse behavior of recording visual evoked potentials (VEPs) as a marker of MDD. We analyzed the amplitudes of VEPs and paired-pulse suppression (PPS) at four different stimulus onset asynchronies (SOAs) spanning 93 ms to 133 ms. Further, the relationship between PPS and the symptom severity of depression was investigated using Spearman's correlation. We found that, whereas the first VEP amplitude remained unchanged, the second VEP amplitude was significantly higher in the MDD group compared to the healthy controls. As a result, the amplitude ratio (second VEP amplitude/first VEP amplitude) increased, indicating reduced PPS and thus increased excitability in the visual cortex. Moreover, we found the amplitude ratios had a significantly positive correlation with the symptom severity of depression in MDD, indicating a clinically useful biomarker for MDD. Our findings provide new insights into the changes in the excitation-inhibition balance of visual cortex in MDD, which could pave the way for specific clinical interventions. Frontiers Media S.A. 2022-03-07 /pmc/articles/PMC8936091/ /pubmed/35321224 http://dx.doi.org/10.3389/fpsyt.2022.844434 Text en Copyright © 2022 Du, Shen, Du, Zhao and Zhou. https://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 Psychiatry
Du, Hongheng
Shen, Xue
Du, Xiaoyan
Zhao, Libo
Zhou, Wenjun
Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title_full Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title_fullStr Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title_full_unstemmed Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title_short Altered Visual Cortical Excitability Is Associated With Psychopathological Symptoms in Major Depressive Disorder
title_sort altered visual cortical excitability is associated with psychopathological symptoms in major depressive disorder
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936091/
https://www.ncbi.nlm.nih.gov/pubmed/35321224
http://dx.doi.org/10.3389/fpsyt.2022.844434
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