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The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials
Elderly depressed patients manifest pronounced executive dysfunction compared with younger subjects with depressive disorder. Aging-related brain changes may result in executive dysfunction in geriatric depression. We investigated the neural correlates of inhibitory control processing in depressed s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811904/ https://www.ncbi.nlm.nih.gov/pubmed/27065830 http://dx.doi.org/10.3389/fnhum.2016.00116 |
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author | Zhang, Bing-Wei Xu, Jing Chang, Yi |
author_facet | Zhang, Bing-Wei Xu, Jing Chang, Yi |
author_sort | Zhang, Bing-Wei |
collection | PubMed |
description | Elderly depressed patients manifest pronounced executive dysfunction compared with younger subjects with depressive disorder. Aging-related brain changes may result in executive dysfunction in geriatric depression. We investigated the neural correlates of inhibitory control processing in depressed subjects at different ages using event-related potentials (ERPs). A equiprobable visual Go/Nogo task was used in 19 young (27.4 ± 5.0 years) and 18 elderly (70.8 ± 6.9 years) depressed subjects and their age-matched healthy controls (20 young subjects, 26.2 ± 3.7 years, and 18 elderly subjects, 68.1 ± 4.8 years). The responses were based on two types of equilateral triangular figures of upright (Go) and inverted triangle (Nogo). The elderly subjects exhibited later N2 and P3 latencies, and larger Go-N2 and P3 amplitudes, compared with the younger subjects. Further, the elderly controls displayed smaller P3 in the central and parietal regions, and yielded larger Nogo-P3 amplitude in the frontal region compared with younger controls. While the young depressed patients yielded smaller P3 amplitude than the controls across frontal, central and parietal regions, elderly depressed patients yielded smaller P3 than the elderly controls only in the frontal region. Our results suggest that the inhibitory control subprocesses are differentially affected by depression and aging. The stimulus response speed and the effort intensity of inhibition control are specifically impaired in the elderly depressed patients. And the diminished amplitudes of frontal P3 in the elderly depression imply a frontal dysfunction mechanism. |
format | Online Article Text |
id | pubmed-4811904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48119042016-04-08 The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials Zhang, Bing-Wei Xu, Jing Chang, Yi Front Hum Neurosci Neuroscience Elderly depressed patients manifest pronounced executive dysfunction compared with younger subjects with depressive disorder. Aging-related brain changes may result in executive dysfunction in geriatric depression. We investigated the neural correlates of inhibitory control processing in depressed subjects at different ages using event-related potentials (ERPs). A equiprobable visual Go/Nogo task was used in 19 young (27.4 ± 5.0 years) and 18 elderly (70.8 ± 6.9 years) depressed subjects and their age-matched healthy controls (20 young subjects, 26.2 ± 3.7 years, and 18 elderly subjects, 68.1 ± 4.8 years). The responses were based on two types of equilateral triangular figures of upright (Go) and inverted triangle (Nogo). The elderly subjects exhibited later N2 and P3 latencies, and larger Go-N2 and P3 amplitudes, compared with the younger subjects. Further, the elderly controls displayed smaller P3 in the central and parietal regions, and yielded larger Nogo-P3 amplitude in the frontal region compared with younger controls. While the young depressed patients yielded smaller P3 amplitude than the controls across frontal, central and parietal regions, elderly depressed patients yielded smaller P3 than the elderly controls only in the frontal region. Our results suggest that the inhibitory control subprocesses are differentially affected by depression and aging. The stimulus response speed and the effort intensity of inhibition control are specifically impaired in the elderly depressed patients. And the diminished amplitudes of frontal P3 in the elderly depression imply a frontal dysfunction mechanism. Frontiers Media S.A. 2016-03-30 /pmc/articles/PMC4811904/ /pubmed/27065830 http://dx.doi.org/10.3389/fnhum.2016.00116 Text en Copyright © 2016 Zhang, Xu and Chang. 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 and reproduction in other forums is permitted, provided the original author(s) or licensor 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 Zhang, Bing-Wei Xu, Jing Chang, Yi The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title | The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title_full | The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title_fullStr | The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title_full_unstemmed | The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title_short | The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials |
title_sort | effect of aging in inhibitory control of major depressive disorder revealed by event-related potentials |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811904/ https://www.ncbi.nlm.nih.gov/pubmed/27065830 http://dx.doi.org/10.3389/fnhum.2016.00116 |
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