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Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study
Various lines of evidence suggest that brain bioenergetics and mitochondrial function may be altered in schizophrenia. On the basis of prior phosphorus-31 ((31)P)-magnetic resonance spectroscopy (MRS), post-mortem and preclinical studies, this study was designed to test the hypothesis that abnormal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290358/ https://www.ncbi.nlm.nih.gov/pubmed/27898072 http://dx.doi.org/10.1038/tp.2016.239 |
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author | Rowland, L M Pradhan, S Korenic, S Wijtenburg, S A Hong, L E Edden, R A Barker, P B |
author_facet | Rowland, L M Pradhan, S Korenic, S Wijtenburg, S A Hong, L E Edden, R A Barker, P B |
author_sort | Rowland, L M |
collection | PubMed |
description | Various lines of evidence suggest that brain bioenergetics and mitochondrial function may be altered in schizophrenia. On the basis of prior phosphorus-31 ((31)P)-magnetic resonance spectroscopy (MRS), post-mortem and preclinical studies, this study was designed to test the hypothesis that abnormal glycolysis leads to elevated lactate concentrations in subjects with schizophrenia. The high sensitivity of 7 Tesla proton ((1)H)-MRS was used to measure brain lactate levels in vivo. Twenty-nine controls and 27 participants with schizophrenia completed the study. MRS scanning was conducted on a Philips ‘Achieva' 7T scanner, and spectra were acquired from a voxel in the anterior cingulate cortex. Patients were assessed for psychiatric symptom severity, and all participants completed the MATRICS Consensus Cognitive Battery (MCCB) and University of California, San Diego Performance-Based Skills Assessment (UPSA). The relationship between lactate, psychiatric symptom severity, MCCB and UPSA was examined. Lactate was significantly higher in patients compared with controls (P=0.013). Higher lactate was associated with lower MCCB (r=−0.36, P=0.01) and UPSA total scores (r=−0.43, P=0.001). We believe this is the first study to report elevated in vivo cerebral lactate levels in schizophrenia. Elevated lactate levels in schizophrenia may reflect increased anaerobic glycolysis possibly because of mitochondrial dysfunction. This study also suggests that altered cerebral bioenergetics contribute to cognitive and functional impairments in schizophrenia. |
format | Online Article Text |
id | pubmed-5290358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52903582017-02-07 Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study Rowland, L M Pradhan, S Korenic, S Wijtenburg, S A Hong, L E Edden, R A Barker, P B Transl Psychiatry Original Article Various lines of evidence suggest that brain bioenergetics and mitochondrial function may be altered in schizophrenia. On the basis of prior phosphorus-31 ((31)P)-magnetic resonance spectroscopy (MRS), post-mortem and preclinical studies, this study was designed to test the hypothesis that abnormal glycolysis leads to elevated lactate concentrations in subjects with schizophrenia. The high sensitivity of 7 Tesla proton ((1)H)-MRS was used to measure brain lactate levels in vivo. Twenty-nine controls and 27 participants with schizophrenia completed the study. MRS scanning was conducted on a Philips ‘Achieva' 7T scanner, and spectra were acquired from a voxel in the anterior cingulate cortex. Patients were assessed for psychiatric symptom severity, and all participants completed the MATRICS Consensus Cognitive Battery (MCCB) and University of California, San Diego Performance-Based Skills Assessment (UPSA). The relationship between lactate, psychiatric symptom severity, MCCB and UPSA was examined. Lactate was significantly higher in patients compared with controls (P=0.013). Higher lactate was associated with lower MCCB (r=−0.36, P=0.01) and UPSA total scores (r=−0.43, P=0.001). We believe this is the first study to report elevated in vivo cerebral lactate levels in schizophrenia. Elevated lactate levels in schizophrenia may reflect increased anaerobic glycolysis possibly because of mitochondrial dysfunction. This study also suggests that altered cerebral bioenergetics contribute to cognitive and functional impairments in schizophrenia. Nature Publishing Group 2016-11 2016-11-29 /pmc/articles/PMC5290358/ /pubmed/27898072 http://dx.doi.org/10.1038/tp.2016.239 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 Rowland, L M Pradhan, S Korenic, S Wijtenburg, S A Hong, L E Edden, R A Barker, P B Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title | Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title_full | Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title_fullStr | Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title_full_unstemmed | Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title_short | Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study |
title_sort | elevated brain lactate in schizophrenia: a 7 t magnetic resonance spectroscopy study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290358/ https://www.ncbi.nlm.nih.gov/pubmed/27898072 http://dx.doi.org/10.1038/tp.2016.239 |
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