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dc.contributor.authorSolvang, Stein-Erik Hafstad
dc.contributor.authorNordrehaug, Jan Erik
dc.contributor.authorAarsland, Dag
dc.contributor.authorLange, Johannes
dc.contributor.authorUeland, Per Magne
dc.contributor.authorMcCann, Adrian
dc.contributor.authorMidttun, Øivind
dc.contributor.authorTell, Grethe S.
dc.contributor.authorMelvær, Giil Lasse
dc.date.accessioned2021-02-08T14:36:04Z
dc.date.available2021-02-08T14:36:04Z
dc.date.created2020-03-10T14:43:45Z
dc.date.issued2019
dc.PublishedInternational Journal of Tryptophan Research. 2019, 12, 1-9.en_US
dc.identifier.issn1178-6469
dc.identifier.urihttps://hdl.handle.net/11250/2726666
dc.description.abstractIntroduction: Circulating tryptophan (Trp) and its downstream metabolites, the kynurenines, are potentially neuroactive. Consequently, they could be associated with neuropsychiatric symptoms and cognitive prognosis in patients with dementia. Objective: The objective of this study was to assess associations between circulating kynurenines, cognitive prognosis, and neuropsychiatric symptoms. Methods: We measured baseline serum Trp, neopterin, pyridoxal 5'-phosphate (PLP), and 9 kynurenines in 155 patients with mild dementia (90 with Alzheimer's disease, 65 with Lewy body dementia). The ratios between kynurenine and Trp and kynurenic acid (KA) to kynurenine (KKR) were calculated. The Mini-Mental State Examination (MMSE) and the Neuropsychiatric Inventory (NPI) were administered at baseline and annually over 5 years. Associations between baseline metabolite concentrations with MMSE and the NPI total score were assessed using a generalized structural equation model (mixed-effects multiprocess model), adjusted for age, sex, current smoking, glomerular filtration rate, and PLP. Post hoc associations between KKRs and individual NPI items were assessed using logistic mixed-effects models. False discovery rate (0.05)-adjusted P values (Q values) are reported. Results: Kynurenine had a nonlinear quadratic relationship with the intercept of the MMSE scores over 5 years (Q < 0.05), but not with the slope of MMSE decline. Kynurenine was associated with a higher NPI total score over time (Q < 0.001). Post hoc, both KKR and KA were associated with more hallucinations (Q < 0.05). Conclusions: Kynurenine has a complex relationship with cognition, where both low and high levels were associated with poor cognitive performance. A higher KKR indicated risk for neuropsychiatric symptoms, especially hallucinations.en_US
dc.language.isoengen_US
dc.publisherSAGE Publicationsen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleKynurenines, Neuropsychiatric Symptoms, and Cognitive Prognosis in Patients with Mild Dementiaen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s) 2019.en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1177/1178646919877883
dc.identifier.cristin1800936
dc.source.journalInternational Journal of Tryptophan Research (IJTR)en_US
dc.source.4012en_US
dc.source.pagenumber1-9en_US
dc.identifier.citationInternational Journal of Tryptophan Research. 2019, 12.


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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