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Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy
There is growing evidence for GABA and glutamate–glutamine dysfunction in the pathogenesis of mood and anxiety disorders. It is important to study this pathology in the early phases of the illness in order to develop new approaches to secondary prevention. New magnetic resonance spectroscopy (MRS) m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581909/ https://www.ncbi.nlm.nih.gov/pubmed/31213596 http://dx.doi.org/10.1038/s41398-019-0500-z |
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author | Hasler, Gregor Buchmann, Andreas Haynes, Melanie Müller, Sabrina Theresia Ghisleni, Carmen Brechbühl, Sarela Tuura, Ruth |
author_facet | Hasler, Gregor Buchmann, Andreas Haynes, Melanie Müller, Sabrina Theresia Ghisleni, Carmen Brechbühl, Sarela Tuura, Ruth |
author_sort | Hasler, Gregor |
collection | PubMed |
description | There is growing evidence for GABA and glutamate–glutamine dysfunction in the pathogenesis of mood and anxiety disorders. It is important to study this pathology in the early phases of the illness in order to develop new approaches to secondary prevention. New magnetic resonance spectroscopy (MRS) measures allow determining glutamine, the principal metabolite of synaptic glutamate that is directly related to glutamate levels in the synaptic cleft, as well as glutamate and GABA. In contrast to previous investigations, this study used community-based recruitment methods and a combined categorical and dimensional approach to psychopathology. In the study protocol, neuroticism was defined as the primary outcome. Neuroticism shares a large proportion of its genetic variance with mood and anxiety disorders. We examined young adult participants recruited from the general population in a cross-sectional study using 3-T 1H-MRS with one voxel in the left dorsolateral prefrontal cortex (DLPFC). The total sample of N = 110 (61 females) included 18 individuals suffering from MDD and 19 individuals suffering from DSM-IV anxiety disorders. We found that glutamine and glutamine-to-glutamate ratio were correlated with neuroticism in the whole sample (r = 0.263, p = 0.005, and n = 110; respectively, r = 0.252, p = 0.008, and n = 110), even when controlling for depression and anxiety disorder diagnoses (for glutamine: beta = 0.220, p = 0.047, and n = 110). Glutamate and GABA were not significantly correlated with neuroticism (r = 0.087, p = 0.365, and n = 110; r = −0.044, p = 0.645, and n = 110). Lack of self-confidence and emotional instability were the clinical correlates of glutamate–glutamine dysfunction. In conclusion, this study suggests that prefrontal glutamine is increased in early phases of mood and anxiety disorders. Further understanding of glutamate–glutamine dysfunction in stress-related disorders may lead to new therapeutic strategies to prevent and treat these disorders. |
format | Online Article Text |
id | pubmed-6581909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65819092019-06-25 Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy Hasler, Gregor Buchmann, Andreas Haynes, Melanie Müller, Sabrina Theresia Ghisleni, Carmen Brechbühl, Sarela Tuura, Ruth Transl Psychiatry Article There is growing evidence for GABA and glutamate–glutamine dysfunction in the pathogenesis of mood and anxiety disorders. It is important to study this pathology in the early phases of the illness in order to develop new approaches to secondary prevention. New magnetic resonance spectroscopy (MRS) measures allow determining glutamine, the principal metabolite of synaptic glutamate that is directly related to glutamate levels in the synaptic cleft, as well as glutamate and GABA. In contrast to previous investigations, this study used community-based recruitment methods and a combined categorical and dimensional approach to psychopathology. In the study protocol, neuroticism was defined as the primary outcome. Neuroticism shares a large proportion of its genetic variance with mood and anxiety disorders. We examined young adult participants recruited from the general population in a cross-sectional study using 3-T 1H-MRS with one voxel in the left dorsolateral prefrontal cortex (DLPFC). The total sample of N = 110 (61 females) included 18 individuals suffering from MDD and 19 individuals suffering from DSM-IV anxiety disorders. We found that glutamine and glutamine-to-glutamate ratio were correlated with neuroticism in the whole sample (r = 0.263, p = 0.005, and n = 110; respectively, r = 0.252, p = 0.008, and n = 110), even when controlling for depression and anxiety disorder diagnoses (for glutamine: beta = 0.220, p = 0.047, and n = 110). Glutamate and GABA were not significantly correlated with neuroticism (r = 0.087, p = 0.365, and n = 110; r = −0.044, p = 0.645, and n = 110). Lack of self-confidence and emotional instability were the clinical correlates of glutamate–glutamine dysfunction. In conclusion, this study suggests that prefrontal glutamine is increased in early phases of mood and anxiety disorders. Further understanding of glutamate–glutamine dysfunction in stress-related disorders may lead to new therapeutic strategies to prevent and treat these disorders. Nature Publishing Group UK 2019-06-18 /pmc/articles/PMC6581909/ /pubmed/31213596 http://dx.doi.org/10.1038/s41398-019-0500-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hasler, Gregor Buchmann, Andreas Haynes, Melanie Müller, Sabrina Theresia Ghisleni, Carmen Brechbühl, Sarela Tuura, Ruth Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title | Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title_full | Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title_fullStr | Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title_full_unstemmed | Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title_short | Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
title_sort | association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581909/ https://www.ncbi.nlm.nih.gov/pubmed/31213596 http://dx.doi.org/10.1038/s41398-019-0500-z |
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