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Association between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy

cris.virtual.author-orcid0000-0002-8311-0138
cris.virtualsource.author-orcid2dcc7f3f-d259-4bc1-91fd-49bd2761f065
cris.virtualsource.author-orcidd57e40d3-a9f4-49b4-a9f9-5bc5998944f6
cris.virtualsource.author-orciddc19bc04-6aa2-4449-9f5d-f6a25ea567a4
cris.virtualsource.author-orciddc1124b5-9bc0-4b02-a654-059b9f7aa613
cris.virtualsource.author-orcidc4b6c976-921d-4cb0-8668-a6d6e04085ff
datacite.rightsopen.access
dc.contributor.authorHasler, Gregor
dc.contributor.authorBuchmann, Andreas
dc.contributor.authorHaynes, Melanie
dc.contributor.authorMüller, Sabrina Theresia
dc.contributor.authorGhisleni, Carmen
dc.contributor.authorBrechbühl, Sarela
dc.contributor.authorTuura, Ruth
dc.date.accessioned2024-10-05T09:47:17Z
dc.date.available2024-10-05T09:47:17Z
dc.date.issued2019
dc.description.abstractThere 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.
dc.description.sponsorshipZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
dc.identifier.doi10.7892/boris.143769
dc.identifier.pmid31213596
dc.identifier.publisherDOI10.1038/s41398-019-0500-z
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/54794
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofTranslational Psychiatry
dc.relation.issn2158-3188
dc.relation.organization33BF865BF1D23C90E053960C5C8246BD
dc.relation.organizationDCD5A442C783E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleAssociation between prefrontal glutamine levels and neuroticism determined using proton magnetic resonance spectroscopy
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage170
oaire.citation.volume9
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
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unibe.date.licenseChanged2020-05-01 13:18:50
unibe.description.ispublishedpub
unibe.eprints.legacyId143769
unibe.refereedtrue
unibe.subtype.articlejournal

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