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Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies

Although the precise pathogenesis of schizophrenia is unknown, genetic, biomarker and imaging studies suggest involvement of the immune system. In this study, we performed a systematic review and meta-analysis of studies investigating factors related to the immune system in postmortem brains of schi...

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Autores principales: van Kesteren, C F M G, Gremmels, H, de Witte, L D, Hol, E M, Van Gool, A R, Falkai, P G, Kahn, R S, Sommer, I E C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404615/
https://www.ncbi.nlm.nih.gov/pubmed/28350400
http://dx.doi.org/10.1038/tp.2017.4
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author van Kesteren, C F M G
Gremmels, H
de Witte, L D
Hol, E M
Van Gool, A R
Falkai, P G
Kahn, R S
Sommer, I E C
author_facet van Kesteren, C F M G
Gremmels, H
de Witte, L D
Hol, E M
Van Gool, A R
Falkai, P G
Kahn, R S
Sommer, I E C
author_sort van Kesteren, C F M G
collection PubMed
description Although the precise pathogenesis of schizophrenia is unknown, genetic, biomarker and imaging studies suggest involvement of the immune system. In this study, we performed a systematic review and meta-analysis of studies investigating factors related to the immune system in postmortem brains of schizophrenia patients and healthy controls. Forty-one studies were included, reporting on 783 patients and 762 controls. We divided these studies into those investigating histological alterations of cellular composition and those assessing molecular parameters; meta-analyses were performed on both categories. Our pooled estimate on cellular level showed a significant increase in the density of microglia (P=0.0028) in the brains of schizophrenia patients compared with controls, albeit with substantial heterogeneity between studies. Meta-regression on brain regions demonstrated this increase was most consistently observed in the temporal cortex. Densities of macroglia (astrocytes and oligodendrocytes) did not differ significantly between schizophrenia patients and healthy controls. The results of postmortem histology are paralleled on the molecular level, where we observed an overall increase in expression of proinflammatory genes on transcript and protein level (P=0.0052) in patients, while anti-inflammatory gene expression levels were not different between schizophrenia and controls. The results of this meta-analysis strengthen the hypothesis that components of the immune system are involved in the pathogenesis of schizophrenia.
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spelling pubmed-54046152017-05-12 Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies van Kesteren, C F M G Gremmels, H de Witte, L D Hol, E M Van Gool, A R Falkai, P G Kahn, R S Sommer, I E C Transl Psychiatry Original Article Although the precise pathogenesis of schizophrenia is unknown, genetic, biomarker and imaging studies suggest involvement of the immune system. In this study, we performed a systematic review and meta-analysis of studies investigating factors related to the immune system in postmortem brains of schizophrenia patients and healthy controls. Forty-one studies were included, reporting on 783 patients and 762 controls. We divided these studies into those investigating histological alterations of cellular composition and those assessing molecular parameters; meta-analyses were performed on both categories. Our pooled estimate on cellular level showed a significant increase in the density of microglia (P=0.0028) in the brains of schizophrenia patients compared with controls, albeit with substantial heterogeneity between studies. Meta-regression on brain regions demonstrated this increase was most consistently observed in the temporal cortex. Densities of macroglia (astrocytes and oligodendrocytes) did not differ significantly between schizophrenia patients and healthy controls. The results of postmortem histology are paralleled on the molecular level, where we observed an overall increase in expression of proinflammatory genes on transcript and protein level (P=0.0052) in patients, while anti-inflammatory gene expression levels were not different between schizophrenia and controls. The results of this meta-analysis strengthen the hypothesis that components of the immune system are involved in the pathogenesis of schizophrenia. Nature Publishing Group 2017-03 2017-03-28 /pmc/articles/PMC5404615/ /pubmed/28350400 http://dx.doi.org/10.1038/tp.2017.4 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 Original Article
van Kesteren, C F M G
Gremmels, H
de Witte, L D
Hol, E M
Van Gool, A R
Falkai, P G
Kahn, R S
Sommer, I E C
Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title_full Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title_fullStr Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title_full_unstemmed Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title_short Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
title_sort immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404615/
https://www.ncbi.nlm.nih.gov/pubmed/28350400
http://dx.doi.org/10.1038/tp.2017.4
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