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Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation

Cortical grey matter volume deficits and neuro-inflammation exist in patients with schizophrenia, although it is not clear whether elevated cytokines contribute to the cortical volume reduction. We quantified cortical and regional brain volumes in fixed postmortem brains from people with schizophren...

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Autores principales: Zhang, Y, Catts, V S, Sheedy, D, McCrossin, T, Kril, J J, Shannon Weickert, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290336/
https://www.ncbi.nlm.nih.gov/pubmed/27959331
http://dx.doi.org/10.1038/tp.2016.238
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author Zhang, Y
Catts, V S
Sheedy, D
McCrossin, T
Kril, J J
Shannon Weickert, C
author_facet Zhang, Y
Catts, V S
Sheedy, D
McCrossin, T
Kril, J J
Shannon Weickert, C
author_sort Zhang, Y
collection PubMed
description Cortical grey matter volume deficits and neuro-inflammation exist in patients with schizophrenia, although it is not clear whether elevated cytokines contribute to the cortical volume reduction. We quantified cortical and regional brain volumes in fixed postmortem brains from people with schizophrenia and matched controls using stereology. Interleukin (IL)-6, IL-1β, IL-8 and SERPINA3 messenger RNAs (mRNAs) were quantified in the contralateral fresh frozen orbitofrontal cortex. We found a small, but significant reduction in cortical grey matter (1.3% F(1,85)=4.478, P=0.037) and superior frontal gyrus (6.5% F(1,80)=5.700, P=0.019) volumes in individuals with schizophrenia compared with controls. Significantly reduced cortical grey matter (9.2% F(1,24)=8.272, P=0.008) and superior frontal gyrus (13.9% F(1,20)=5.374, P=0.031) volumes were found in cases with schizophrenia and ‘high inflammation' status relative to schizophrenia cases with ‘low inflammation' status in the prefrontal cortex. The expression of inflammatory mRNAs in the orbitofrontal cortex was significantly correlated with those in dorsolateral prefrontal cortex (all r>0.417, all P<0.022), except for IL-8. Moreover, average daily and lifetime antipsychotic intake negatively correlated with cortical grey matter and superior frontal gyrus volumes (all r<−0.362, all P<0.05). The results suggest that the reduction in cortical grey matter volume in people with schizophrenia is exaggerated in those who have high expression of inflammatory cytokines. Further, antipsychotic medication intake does not appear to ameliorate the reduction in brain volume.
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spelling pubmed-52903362017-02-07 Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation Zhang, Y Catts, V S Sheedy, D McCrossin, T Kril, J J Shannon Weickert, C Transl Psychiatry Original Article Cortical grey matter volume deficits and neuro-inflammation exist in patients with schizophrenia, although it is not clear whether elevated cytokines contribute to the cortical volume reduction. We quantified cortical and regional brain volumes in fixed postmortem brains from people with schizophrenia and matched controls using stereology. Interleukin (IL)-6, IL-1β, IL-8 and SERPINA3 messenger RNAs (mRNAs) were quantified in the contralateral fresh frozen orbitofrontal cortex. We found a small, but significant reduction in cortical grey matter (1.3% F(1,85)=4.478, P=0.037) and superior frontal gyrus (6.5% F(1,80)=5.700, P=0.019) volumes in individuals with schizophrenia compared with controls. Significantly reduced cortical grey matter (9.2% F(1,24)=8.272, P=0.008) and superior frontal gyrus (13.9% F(1,20)=5.374, P=0.031) volumes were found in cases with schizophrenia and ‘high inflammation' status relative to schizophrenia cases with ‘low inflammation' status in the prefrontal cortex. The expression of inflammatory mRNAs in the orbitofrontal cortex was significantly correlated with those in dorsolateral prefrontal cortex (all r>0.417, all P<0.022), except for IL-8. Moreover, average daily and lifetime antipsychotic intake negatively correlated with cortical grey matter and superior frontal gyrus volumes (all r<−0.362, all P<0.05). The results suggest that the reduction in cortical grey matter volume in people with schizophrenia is exaggerated in those who have high expression of inflammatory cytokines. Further, antipsychotic medication intake does not appear to ameliorate the reduction in brain volume. Nature Publishing Group 2016-12 2016-12-13 /pmc/articles/PMC5290336/ /pubmed/27959331 http://dx.doi.org/10.1038/tp.2016.238 Text en Copyright © 2016 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
Zhang, Y
Catts, V S
Sheedy, D
McCrossin, T
Kril, J J
Shannon Weickert, C
Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title_full Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title_fullStr Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title_full_unstemmed Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title_short Cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
title_sort cortical grey matter volume reduction in people with schizophrenia is associated with neuro-inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290336/
https://www.ncbi.nlm.nih.gov/pubmed/27959331
http://dx.doi.org/10.1038/tp.2016.238
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