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Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems

This study examined the impact of depressive disorders, anxiety disorders and the comorbidity of these disorders on the regional electrophysiological features of brain activity. Sixty-four-channel event-related potentials (ERP) were acquired during a visual oddball task in patients with depressive d...

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Autores principales: Li, Yuezhi, Wang, Wuyi, Liu, Tiebang, Ren, Lijie, Zhou, Yunfei, Yu, Changhong, Qu, Xingda, Hu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657106/
https://www.ncbi.nlm.nih.gov/pubmed/26598026
http://dx.doi.org/10.1038/srep17138
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author Li, Yuezhi
Wang, Wuyi
Liu, Tiebang
Ren, Lijie
Zhou, Yunfei
Yu, Changhong
Qu, Xingda
Hu, Yong
author_facet Li, Yuezhi
Wang, Wuyi
Liu, Tiebang
Ren, Lijie
Zhou, Yunfei
Yu, Changhong
Qu, Xingda
Hu, Yong
author_sort Li, Yuezhi
collection PubMed
description This study examined the impact of depressive disorders, anxiety disorders and the comorbidity of these disorders on the regional electrophysiological features of brain activity. Sixty-four-channel event-related potentials (ERP) were acquired during a visual oddball task in patients with depressive disorder, patients with anxiety disorders, patients with comorbid depressive and anxiety disorders and healthy subjects. An fMRI-constrained source model was applied to ERP to identify different cortical activities in the patient and control groups. Comorbid patients showed an abnormal frontal-greater-than-parietal P3b topography in the right hemisphere and the highest P3a amplitude at frontal and central sites at the scalp midline. For P3b, depressed patients showed decreased right-lateralized activity in the precentral sulcus (PrCS) and posterior parietal cortex (PPC). Anxious patients demonstrated hyperactive prefrontal cortices (PFC). Comorbid patients presented decreased activity in the cingulate gyrus, right PrCS and right PPC and increased activity in the left PFC and left insular (INS). For P3a, hyperactive left PrCS was found in comorbid patients. Comorbid patients showed both anxiety-related and depression-related activity. A superimposition effect of depression and anxiety was identified with (1) aggravated hypo-function of the right-lateralized dorsal attention and salience networks and (2) complicated anxiety-related hyper-function of the left-lateralized ventral attention and salience networks.
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spelling pubmed-46571062015-11-30 Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems Li, Yuezhi Wang, Wuyi Liu, Tiebang Ren, Lijie Zhou, Yunfei Yu, Changhong Qu, Xingda Hu, Yong Sci Rep Article This study examined the impact of depressive disorders, anxiety disorders and the comorbidity of these disorders on the regional electrophysiological features of brain activity. Sixty-four-channel event-related potentials (ERP) were acquired during a visual oddball task in patients with depressive disorder, patients with anxiety disorders, patients with comorbid depressive and anxiety disorders and healthy subjects. An fMRI-constrained source model was applied to ERP to identify different cortical activities in the patient and control groups. Comorbid patients showed an abnormal frontal-greater-than-parietal P3b topography in the right hemisphere and the highest P3a amplitude at frontal and central sites at the scalp midline. For P3b, depressed patients showed decreased right-lateralized activity in the precentral sulcus (PrCS) and posterior parietal cortex (PPC). Anxious patients demonstrated hyperactive prefrontal cortices (PFC). Comorbid patients presented decreased activity in the cingulate gyrus, right PrCS and right PPC and increased activity in the left PFC and left insular (INS). For P3a, hyperactive left PrCS was found in comorbid patients. Comorbid patients showed both anxiety-related and depression-related activity. A superimposition effect of depression and anxiety was identified with (1) aggravated hypo-function of the right-lateralized dorsal attention and salience networks and (2) complicated anxiety-related hyper-function of the left-lateralized ventral attention and salience networks. Nature Publishing Group 2015-11-24 /pmc/articles/PMC4657106/ /pubmed/26598026 http://dx.doi.org/10.1038/srep17138 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Li, Yuezhi
Wang, Wuyi
Liu, Tiebang
Ren, Lijie
Zhou, Yunfei
Yu, Changhong
Qu, Xingda
Hu, Yong
Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title_full Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title_fullStr Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title_full_unstemmed Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title_short Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems
title_sort source analysis of p3a and p3b components to investigate interaction of depression and anxiety in attentional systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657106/
https://www.ncbi.nlm.nih.gov/pubmed/26598026
http://dx.doi.org/10.1038/srep17138
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