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Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia
Frontotemporal dysconnectivity is a key pathology in schizophrenia. The specific nature of this dysconnectivity is unknown, but animal models imply dysfunctional theta phase coupling between hippocampus and medial prefrontal cortex (mPFC). We tested this hypothesis by examining neural dynamics in 18...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174039/ https://www.ncbi.nlm.nih.gov/pubmed/32236540 http://dx.doi.org/10.1093/brain/awaa035 |
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author | Adams, Rick A Bush, Daniel Zheng, Fanfan Meyer, Sofie S Kaplan, Raphael Orfanos, Stelios Marques, Tiago Reis Howes, Oliver D Burgess, Neil |
author_facet | Adams, Rick A Bush, Daniel Zheng, Fanfan Meyer, Sofie S Kaplan, Raphael Orfanos, Stelios Marques, Tiago Reis Howes, Oliver D Burgess, Neil |
author_sort | Adams, Rick A |
collection | PubMed |
description | Frontotemporal dysconnectivity is a key pathology in schizophrenia. The specific nature of this dysconnectivity is unknown, but animal models imply dysfunctional theta phase coupling between hippocampus and medial prefrontal cortex (mPFC). We tested this hypothesis by examining neural dynamics in 18 participants with a schizophrenia diagnosis, both medicated and unmedicated; and 26 age, sex and IQ matched control subjects. All participants completed two tasks known to elicit hippocampal-prefrontal theta coupling: a spatial memory task (during magnetoencephalography) and a memory integration task. In addition, an overlapping group of 33 schizophrenia and 29 control subjects underwent PET to measure the availability of GABA(A)Rs expressing the α5 subunit (concentrated on hippocampal somatostatin interneurons). We demonstrate—in the spatial memory task, during memory recall—that theta power increases in left medial temporal lobe (mTL) are impaired in schizophrenia, as is theta phase coupling between mPFC and mTL. Importantly, the latter cannot be explained by theta power changes, head movement, antipsychotics, cannabis use, or IQ, and is not found in other frequency bands. Moreover, mPFC-mTL theta coupling correlated strongly with performance in controls, but not in subjects with schizophrenia, who were mildly impaired at the spatial memory task and no better than chance on the memory integration task. Finally, mTL regions showing reduced phase coupling in schizophrenia magnetoencephalography participants overlapped substantially with areas of diminished α5-GABA(A)R availability in the wider schizophrenia PET sample. These results indicate that mPFC-mTL dysconnectivity in schizophrenia is due to a loss of theta phase coupling, and imply α5-GABA(A)Rs (and the cells that express them) have a role in this process. |
format | Online Article Text |
id | pubmed-7174039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71740392020-04-27 Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia Adams, Rick A Bush, Daniel Zheng, Fanfan Meyer, Sofie S Kaplan, Raphael Orfanos, Stelios Marques, Tiago Reis Howes, Oliver D Burgess, Neil Brain Original Articles Frontotemporal dysconnectivity is a key pathology in schizophrenia. The specific nature of this dysconnectivity is unknown, but animal models imply dysfunctional theta phase coupling between hippocampus and medial prefrontal cortex (mPFC). We tested this hypothesis by examining neural dynamics in 18 participants with a schizophrenia diagnosis, both medicated and unmedicated; and 26 age, sex and IQ matched control subjects. All participants completed two tasks known to elicit hippocampal-prefrontal theta coupling: a spatial memory task (during magnetoencephalography) and a memory integration task. In addition, an overlapping group of 33 schizophrenia and 29 control subjects underwent PET to measure the availability of GABA(A)Rs expressing the α5 subunit (concentrated on hippocampal somatostatin interneurons). We demonstrate—in the spatial memory task, during memory recall—that theta power increases in left medial temporal lobe (mTL) are impaired in schizophrenia, as is theta phase coupling between mPFC and mTL. Importantly, the latter cannot be explained by theta power changes, head movement, antipsychotics, cannabis use, or IQ, and is not found in other frequency bands. Moreover, mPFC-mTL theta coupling correlated strongly with performance in controls, but not in subjects with schizophrenia, who were mildly impaired at the spatial memory task and no better than chance on the memory integration task. Finally, mTL regions showing reduced phase coupling in schizophrenia magnetoencephalography participants overlapped substantially with areas of diminished α5-GABA(A)R availability in the wider schizophrenia PET sample. These results indicate that mPFC-mTL dysconnectivity in schizophrenia is due to a loss of theta phase coupling, and imply α5-GABA(A)Rs (and the cells that express them) have a role in this process. Oxford University Press 2020-04 2020-04-01 /pmc/articles/PMC7174039/ /pubmed/32236540 http://dx.doi.org/10.1093/brain/awaa035 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Adams, Rick A Bush, Daniel Zheng, Fanfan Meyer, Sofie S Kaplan, Raphael Orfanos, Stelios Marques, Tiago Reis Howes, Oliver D Burgess, Neil Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title | Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title_full | Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title_fullStr | Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title_full_unstemmed | Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title_short | Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
title_sort | impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174039/ https://www.ncbi.nlm.nih.gov/pubmed/32236540 http://dx.doi.org/10.1093/brain/awaa035 |
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