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Frontal and superior temporal auditory processing abnormalities in schizophrenia()
BACKGROUND: Although magnetoencephalography (MEG) studies show superior temporal gyrus (STG) auditory processing abnormalities in schizophrenia at 50 and 100 ms, EEG and corticography studies suggest involvement of additional brain areas (e.g., frontal areas) during this interval. Study goals were t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777790/ https://www.ncbi.nlm.nih.gov/pubmed/24179821 http://dx.doi.org/10.1016/j.nicl.2013.05.002 |
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author | Chen, Yu-Han Edgar, J. Christopher Huang, Mingxiong Hunter, Michael A. Epstein, Emerson Howell, Breannan Lu, Brett Y. Bustillo, Juan Miller, Gregory A. Cañive, José M. |
author_facet | Chen, Yu-Han Edgar, J. Christopher Huang, Mingxiong Hunter, Michael A. Epstein, Emerson Howell, Breannan Lu, Brett Y. Bustillo, Juan Miller, Gregory A. Cañive, José M. |
author_sort | Chen, Yu-Han |
collection | PubMed |
description | BACKGROUND: Although magnetoencephalography (MEG) studies show superior temporal gyrus (STG) auditory processing abnormalities in schizophrenia at 50 and 100 ms, EEG and corticography studies suggest involvement of additional brain areas (e.g., frontal areas) during this interval. Study goals were to identify 30 to 130 ms auditory encoding processes in schizophrenia (SZ) and healthy controls (HC) and group differences throughout the cortex. METHODS: The standard paired-click task was administered to 19 SZ and 21 HC subjects during MEG recording. Vector-based Spatial–temporal Analysis using L1-minimum-norm (VESTAL) provided 4D maps of activity from 30 to 130 ms. Within-group t-tests compared post-stimulus 50 ms and 100 ms activity to baseline. Between-group t-tests examined 50 and 100 ms group differences. RESULTS: Bilateral 50 and 100 ms STG activity was observed in both groups. HC had stronger bilateral 50 and 100 ms STG activity than SZ. In addition to the STG group difference, non-STG activity was also observed in both groups. For example, whereas HC had stronger left and right inferior frontal gyrus activity than SZ, SZ had stronger right superior frontal gyrus and left supramarginal gyrus activity than HC. CONCLUSIONS: Less STG activity was observed in SZ than HC, indicating encoding problems in SZ. Yet auditory encoding abnormalities are not specific to STG, as group differences were observed in frontal and SMG areas. Thus, present findings indicate that individuals with SZ show abnormalities in multiple nodes of a concurrently activated auditory network. |
format | Online Article Text |
id | pubmed-3777790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37777902013-10-31 Frontal and superior temporal auditory processing abnormalities in schizophrenia() Chen, Yu-Han Edgar, J. Christopher Huang, Mingxiong Hunter, Michael A. Epstein, Emerson Howell, Breannan Lu, Brett Y. Bustillo, Juan Miller, Gregory A. Cañive, José M. Neuroimage Clin Article BACKGROUND: Although magnetoencephalography (MEG) studies show superior temporal gyrus (STG) auditory processing abnormalities in schizophrenia at 50 and 100 ms, EEG and corticography studies suggest involvement of additional brain areas (e.g., frontal areas) during this interval. Study goals were to identify 30 to 130 ms auditory encoding processes in schizophrenia (SZ) and healthy controls (HC) and group differences throughout the cortex. METHODS: The standard paired-click task was administered to 19 SZ and 21 HC subjects during MEG recording. Vector-based Spatial–temporal Analysis using L1-minimum-norm (VESTAL) provided 4D maps of activity from 30 to 130 ms. Within-group t-tests compared post-stimulus 50 ms and 100 ms activity to baseline. Between-group t-tests examined 50 and 100 ms group differences. RESULTS: Bilateral 50 and 100 ms STG activity was observed in both groups. HC had stronger bilateral 50 and 100 ms STG activity than SZ. In addition to the STG group difference, non-STG activity was also observed in both groups. For example, whereas HC had stronger left and right inferior frontal gyrus activity than SZ, SZ had stronger right superior frontal gyrus and left supramarginal gyrus activity than HC. CONCLUSIONS: Less STG activity was observed in SZ than HC, indicating encoding problems in SZ. Yet auditory encoding abnormalities are not specific to STG, as group differences were observed in frontal and SMG areas. Thus, present findings indicate that individuals with SZ show abnormalities in multiple nodes of a concurrently activated auditory network. Elsevier 2013-05-15 /pmc/articles/PMC3777790/ /pubmed/24179821 http://dx.doi.org/10.1016/j.nicl.2013.05.002 Text en © 2013 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Chen, Yu-Han Edgar, J. Christopher Huang, Mingxiong Hunter, Michael A. Epstein, Emerson Howell, Breannan Lu, Brett Y. Bustillo, Juan Miller, Gregory A. Cañive, José M. Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title | Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title_full | Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title_fullStr | Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title_full_unstemmed | Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title_short | Frontal and superior temporal auditory processing abnormalities in schizophrenia() |
title_sort | frontal and superior temporal auditory processing abnormalities in schizophrenia() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777790/ https://www.ncbi.nlm.nih.gov/pubmed/24179821 http://dx.doi.org/10.1016/j.nicl.2013.05.002 |
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