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dc.contributor.authorEide, Per Kristian
dc.contributor.authorLashkarivand, Aslan
dc.contributor.authorPripp, Are Hugo
dc.contributor.authorValnes, Lars Magnus
dc.contributor.authorHovd, Markus Herberg
dc.contributor.authorRingstad, Geir
dc.contributor.authorBlennow, Kaj
dc.contributor.authorZetterberg, Henrik
dc.date.accessioned2024-01-10T10:19:28Z
dc.date.available2024-01-10T10:19:28Z
dc.date.created2023-06-27T14:32:44Z
dc.date.issued2023
dc.identifier.citationNature Communications. 2023, 14 1-14.en_US
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/11250/3110820
dc.description.abstractClearance of neurotoxic brain proteins via cerebrospinal fluid (CSF) to blood has recently emerged to be crucial, and plasma biomarkers of neurodegen- eration were newly introduced to predict neurological disease. This study examines in 106 individuals with neurological disorders associations between plasma biomarkers [40 and 42 amino acid-long amyloid-β (Aβ40 and Aβ42), total-tau, glial fibrillary acidic protein (GFAP), and neurofilament light (NfL)] and magnetic resonance imaging measures of CSF-mediated clearance from brain via extra-vascular pathways (proxy of glymphatic function) and CSF-to- blood clearance variables from pharmacokinetic modeling (proxy of menin- geal lymphatic egress). We also examine how biomarkers vary during daytime and associate with subjective sleep quality. Plasma concentrations of neuro- degeneration markers associate with indices of glymphatic and meningeal lymphatic functions in individual- and disease-specific manners, vary during daytime, but are unaffected by sleep quality. The results suggest that plasma concentrations of neurodegeneration biomarkers associate with measures of glymphatic and meningeal lymphatic function.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titlePlasma neurodegeneration biomarker concentrations associate with glymphatic and meningeal lymphatic measures in neurological disordersen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1038/s41467-023-37685-5
dc.identifier.cristin2158758
dc.source.journalNature Communicationsen_US
dc.source.volume14en_US
dc.source.pagenumber1-14en_US


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