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Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study
H-Magnetic Resonance Spectroscopy ((1)H-MRS) can offer insights in various neuropathologies by measuring metabolite levels in the brain. In the current study we investigated the levels of glutamate + glutamine (Glx, neurotransmitter and precursor) and N-Acetyl Aspartate + glutamic acid (NAA + NAAG;...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763193/ https://www.ncbi.nlm.nih.gov/pubmed/26903078 http://dx.doi.org/10.1038/srep21873 |
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author | Liemburg, Edith Sibeijn-Kuiper, Anita Bais, Leonie Pijnenborg, Gerdina Knegtering, Henderikus van der Velde, Jorien Opmeer, Esther de Vos, Annerieke Dlabac-De Lange, Jozarni Wunderink, Lex Aleman, André |
author_facet | Liemburg, Edith Sibeijn-Kuiper, Anita Bais, Leonie Pijnenborg, Gerdina Knegtering, Henderikus van der Velde, Jorien Opmeer, Esther de Vos, Annerieke Dlabac-De Lange, Jozarni Wunderink, Lex Aleman, André |
author_sort | Liemburg, Edith |
collection | PubMed |
description | H-Magnetic Resonance Spectroscopy ((1)H-MRS) can offer insights in various neuropathologies by measuring metabolite levels in the brain. In the current study we investigated the levels of glutamate + glutamine (Glx, neurotransmitter and precursor) and N-Acetyl Aspartate + glutamic acid (NAA + NAAG; neuronal viability) in the prefrontal cortex of patients with a psychotic disorder and people at Ultra High Risk (UHR) for psychosis. A (1)H-MRS spectrum was acquired in 31 patients with a recent onset psychotic disorder and 60 with a chronic state, 16 UHR patients and 36 healthy controls. Absolute metabolite levels were calculated using LCModel with a reference water peak. Groups were compared while taking into account age and partial volume effects. Moreover, we investigated associations with positive and negative symptoms, duration of illness, and antipsychotic treatment in patients. The most notable finding is that chronicity of schizophrenia was related to decreased levels of Glx and NAA. On the other hand, although on an exploratory note, UHR showed increased levels of prefrontal Glx and NAA levels with increasing age. Our results may indicate an initial Glx and NAA increase and subsequent decrease during illness progression that may be related to the neurotoxic effects of glutamate. |
format | Online Article Text |
id | pubmed-4763193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47631932016-03-01 Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study Liemburg, Edith Sibeijn-Kuiper, Anita Bais, Leonie Pijnenborg, Gerdina Knegtering, Henderikus van der Velde, Jorien Opmeer, Esther de Vos, Annerieke Dlabac-De Lange, Jozarni Wunderink, Lex Aleman, André Sci Rep Article H-Magnetic Resonance Spectroscopy ((1)H-MRS) can offer insights in various neuropathologies by measuring metabolite levels in the brain. In the current study we investigated the levels of glutamate + glutamine (Glx, neurotransmitter and precursor) and N-Acetyl Aspartate + glutamic acid (NAA + NAAG; neuronal viability) in the prefrontal cortex of patients with a psychotic disorder and people at Ultra High Risk (UHR) for psychosis. A (1)H-MRS spectrum was acquired in 31 patients with a recent onset psychotic disorder and 60 with a chronic state, 16 UHR patients and 36 healthy controls. Absolute metabolite levels were calculated using LCModel with a reference water peak. Groups were compared while taking into account age and partial volume effects. Moreover, we investigated associations with positive and negative symptoms, duration of illness, and antipsychotic treatment in patients. The most notable finding is that chronicity of schizophrenia was related to decreased levels of Glx and NAA. On the other hand, although on an exploratory note, UHR showed increased levels of prefrontal Glx and NAA levels with increasing age. Our results may indicate an initial Glx and NAA increase and subsequent decrease during illness progression that may be related to the neurotoxic effects of glutamate. Nature Publishing Group 2016-02-23 /pmc/articles/PMC4763193/ /pubmed/26903078 http://dx.doi.org/10.1038/srep21873 Text en Copyright © 2016, 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 Liemburg, Edith Sibeijn-Kuiper, Anita Bais, Leonie Pijnenborg, Gerdina Knegtering, Henderikus van der Velde, Jorien Opmeer, Esther de Vos, Annerieke Dlabac-De Lange, Jozarni Wunderink, Lex Aleman, André Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title | Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title_full | Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title_fullStr | Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title_full_unstemmed | Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title_short | Prefrontal NAA and Glx Levels in Different Stages of Psychotic Disorders: a 3T (1)H-MRS Study |
title_sort | prefrontal naa and glx levels in different stages of psychotic disorders: a 3t (1)h-mrs study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763193/ https://www.ncbi.nlm.nih.gov/pubmed/26903078 http://dx.doi.org/10.1038/srep21873 |
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