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Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study

The aim of this study was to investigate the neural substrate underlying quality of life (QoL) and to demonstrate the microstructural abnormalities associated with impaired QoL in a large sample of patients with schizophrenia, using magnetisation transfer imaging. A total of 81 right-handed men with...

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Autores principales: Catherine, Faget-Agius, Boyer, Laurent, Jonathan, Wirsich, Jean-Philippe, Ranjeva, Raphaelle, Richieri, Elisabeth, Soulier, Sylviane, Confort-Gouny, Pascal, Auquier, Maxime, Guye, Christophe, Lançon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668560/
https://www.ncbi.nlm.nih.gov/pubmed/26632639
http://dx.doi.org/10.1038/srep17650
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author Catherine, Faget-Agius
Boyer, Laurent
Jonathan, Wirsich
Jean-Philippe, Ranjeva
Raphaelle, Richieri
Elisabeth, Soulier
Sylviane, Confort-Gouny
Pascal, Auquier
Maxime, Guye
Christophe, Lançon
author_facet Catherine, Faget-Agius
Boyer, Laurent
Jonathan, Wirsich
Jean-Philippe, Ranjeva
Raphaelle, Richieri
Elisabeth, Soulier
Sylviane, Confort-Gouny
Pascal, Auquier
Maxime, Guye
Christophe, Lançon
author_sort Catherine, Faget-Agius
collection PubMed
description The aim of this study was to investigate the neural substrate underlying quality of life (QoL) and to demonstrate the microstructural abnormalities associated with impaired QoL in a large sample of patients with schizophrenia, using magnetisation transfer imaging. A total of 81 right-handed men with a diagnosis of schizophrenia and 25 age- and sex-similar healthy controls were included and underwent a 3T MRI with magnetization transfer ratio (MTR) to detect microstructural abnormalities. Compared with healthy controls, patients with schizophrenia had grey matter (GM) decreased MTR values in the temporal lobe (BA21, BA37 and BA38), the bilateral insula, the occipital lobe (BA17, BA18 and BA19) and the cerebellum. Patients with impaired QoL had lower GM MTR values relative to patients with preserved QoL in the bilateral temporal pole (BA38), the bilateral insula, the secondary visual cortex (BA18), the vermis and the cerebellum. Significant correlations between MTR values and QoL scores (p < 0.005) were observed in the GM of patients in the right temporal pole (BA38), the bilateral insula, the vermis and the right cerebellum. Our study shows that QoL impairment in patients with schizophrenia is related to the microstructural changes in an extensive network, suggesting that QoL is a bio-psychosocial marker.
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spelling pubmed-46685602015-12-09 Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study Catherine, Faget-Agius Boyer, Laurent Jonathan, Wirsich Jean-Philippe, Ranjeva Raphaelle, Richieri Elisabeth, Soulier Sylviane, Confort-Gouny Pascal, Auquier Maxime, Guye Christophe, Lançon Sci Rep Article The aim of this study was to investigate the neural substrate underlying quality of life (QoL) and to demonstrate the microstructural abnormalities associated with impaired QoL in a large sample of patients with schizophrenia, using magnetisation transfer imaging. A total of 81 right-handed men with a diagnosis of schizophrenia and 25 age- and sex-similar healthy controls were included and underwent a 3T MRI with magnetization transfer ratio (MTR) to detect microstructural abnormalities. Compared with healthy controls, patients with schizophrenia had grey matter (GM) decreased MTR values in the temporal lobe (BA21, BA37 and BA38), the bilateral insula, the occipital lobe (BA17, BA18 and BA19) and the cerebellum. Patients with impaired QoL had lower GM MTR values relative to patients with preserved QoL in the bilateral temporal pole (BA38), the bilateral insula, the secondary visual cortex (BA18), the vermis and the cerebellum. Significant correlations between MTR values and QoL scores (p < 0.005) were observed in the GM of patients in the right temporal pole (BA38), the bilateral insula, the vermis and the right cerebellum. Our study shows that QoL impairment in patients with schizophrenia is related to the microstructural changes in an extensive network, suggesting that QoL is a bio-psychosocial marker. Nature Publishing Group 2015-12-03 /pmc/articles/PMC4668560/ /pubmed/26632639 http://dx.doi.org/10.1038/srep17650 Text en Copyright © 2015, Macmillan Publishers Limited 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 Article
Catherine, Faget-Agius
Boyer, Laurent
Jonathan, Wirsich
Jean-Philippe, Ranjeva
Raphaelle, Richieri
Elisabeth, Soulier
Sylviane, Confort-Gouny
Pascal, Auquier
Maxime, Guye
Christophe, Lançon
Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title_full Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title_fullStr Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title_full_unstemmed Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title_short Neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
title_sort neural substrate of quality of life in patients with schizophrenia: a magnetisation transfer imaging study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668560/
https://www.ncbi.nlm.nih.gov/pubmed/26632639
http://dx.doi.org/10.1038/srep17650
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