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Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis

Data from animal models and from postmortem studies suggest that schizophrenia is associated with brain GABAergic dysfunction. The extent to which this is reflected in data from in vivo studies of GABA function in schizophrenia is unclear. The Medline database was searched to identify articles publi...

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Autores principales: Egerton, A, Modinos, G, Ferrera, D, McGuire, P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537645/
https://www.ncbi.nlm.nih.gov/pubmed/28585933
http://dx.doi.org/10.1038/tp.2017.124
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author Egerton, A
Modinos, G
Ferrera, D
McGuire, P
author_facet Egerton, A
Modinos, G
Ferrera, D
McGuire, P
author_sort Egerton, A
collection PubMed
description Data from animal models and from postmortem studies suggest that schizophrenia is associated with brain GABAergic dysfunction. The extent to which this is reflected in data from in vivo studies of GABA function in schizophrenia is unclear. The Medline database was searched to identify articles published until 21 October 2016. The search terms included GABA, proton magnetic resonance spectroscopy ((1)H-MRS), positron emission tomography (PET), single photon emission computed tomography (SPECT), schizophrenia and psychosis. Sixteen GABA (1)H-MRS studies (538 controls, 526 patients) and seven PET/SPECT studies of GABA(A)/benzodiazepine receptor (GABA(A)/BZR) availability (118 controls, 113 patients) were identified. Meta-analyses of (1)H-MRS GABA in the medial prefrontal cortex (mPFC), parietal/occipital cortex (POC) and striatum did not show significant group differences (mFC: g=−0.3, 409 patients, 495 controls, 95% confidence interval (CI): −0.6 to 0.1; POC: g=−0.3, 139 patients, 111 controls, 95% CI: −0.9 to 0.3; striatum: g=−0.004, 123 patients, 95 controls, 95% CI: −0.7 to 0.7). Heterogeneity across studies was high (I(2)>50%), and this was not explained by subsequent moderator or meta-regression analyses. There were insufficient PET/SPECT receptor availability studies for meta-analyses, but a systematic review did not suggest replicable group differences in regional GABA(A)/BZR availability. The current literature does not reveal consistent alterations in in vivo GABA neuroimaging measures in schizophrenia, as might be hypothesized from animal models and postmortem data. The analysis highlights the need for further GABA neuroimaging studies with improved methodology and addressing potential sources of heterogeneity.
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spelling pubmed-55376452017-08-02 Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis Egerton, A Modinos, G Ferrera, D McGuire, P Transl Psychiatry Review Data from animal models and from postmortem studies suggest that schizophrenia is associated with brain GABAergic dysfunction. The extent to which this is reflected in data from in vivo studies of GABA function in schizophrenia is unclear. The Medline database was searched to identify articles published until 21 October 2016. The search terms included GABA, proton magnetic resonance spectroscopy ((1)H-MRS), positron emission tomography (PET), single photon emission computed tomography (SPECT), schizophrenia and psychosis. Sixteen GABA (1)H-MRS studies (538 controls, 526 patients) and seven PET/SPECT studies of GABA(A)/benzodiazepine receptor (GABA(A)/BZR) availability (118 controls, 113 patients) were identified. Meta-analyses of (1)H-MRS GABA in the medial prefrontal cortex (mPFC), parietal/occipital cortex (POC) and striatum did not show significant group differences (mFC: g=−0.3, 409 patients, 495 controls, 95% confidence interval (CI): −0.6 to 0.1; POC: g=−0.3, 139 patients, 111 controls, 95% CI: −0.9 to 0.3; striatum: g=−0.004, 123 patients, 95 controls, 95% CI: −0.7 to 0.7). Heterogeneity across studies was high (I(2)>50%), and this was not explained by subsequent moderator or meta-regression analyses. There were insufficient PET/SPECT receptor availability studies for meta-analyses, but a systematic review did not suggest replicable group differences in regional GABA(A)/BZR availability. The current literature does not reveal consistent alterations in in vivo GABA neuroimaging measures in schizophrenia, as might be hypothesized from animal models and postmortem data. The analysis highlights the need for further GABA neuroimaging studies with improved methodology and addressing potential sources of heterogeneity. Nature Publishing Group 2017-06 2017-06-06 /pmc/articles/PMC5537645/ /pubmed/28585933 http://dx.doi.org/10.1038/tp.2017.124 Text en Copyright © 2017 The Author(s) 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 Review
Egerton, A
Modinos, G
Ferrera, D
McGuire, P
Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title_full Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title_fullStr Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title_full_unstemmed Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title_short Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis
title_sort neuroimaging studies of gaba in schizophrenia: a systematic review with meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537645/
https://www.ncbi.nlm.nih.gov/pubmed/28585933
http://dx.doi.org/10.1038/tp.2017.124
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