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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...

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Autores principales: Adams, Rick A, Bush, Daniel, Zheng, Fanfan, Meyer, Sofie S, Kaplan, Raphael, Orfanos, Stelios, Marques, Tiago Reis, Howes, Oliver D, Burgess, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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.
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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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