Show simple item record

dc.contributor.authorLim, Bryant
dc.contributor.authorGrøntvedt, Gøril Rolfseng
dc.contributor.authorBathala, Pradeepthi
dc.contributor.authorKale, Shraddha S.
dc.contributor.authorCampbell, Christopher T.
dc.contributor.authorStengelin, Martin
dc.contributor.authorSando, Sigrid Botne
dc.contributor.authorPrassas, Ioannis
dc.contributor.authorDiamandis, Eleftherios P.
dc.contributor.authorBråthen, Geir
dc.date.accessioned2021-09-16T08:30:13Z
dc.date.available2021-09-16T08:30:13Z
dc.date.created2021-09-01T09:36:57Z
dc.date.issued2021
dc.identifier.citationNeurobiology of Aging. 2021, 107, 78-85.en_US
dc.identifier.issn0197-4580
dc.identifier.urihttps://hdl.handle.net/11250/2778482
dc.description.abstractNeurofilament light (NfL) is a promising biomarker of neurodegeneration in Alzheimer's disease (AD). In this study, cerebrospinal fluid (CSF) NfL was measured in a 24-month longitudinal cohort consisting of control (n = 52), amnestic mild cognitive impairment (aMCI) (n = 55), and probable AD dementia (n = 28) individuals. The cohort was reevaluated after 6-10 years. Baseline CSF NfL was significantly elevated in aMCI and probable AD dementia groups compared to controls (p < 0.0001). CSF NfL was significantly lower in stable aMCI patients compared to aMCI patients who converted to probable AD dementia within the 24-month period (p = 0.004). Substituting T-tau for NfL in the core AD biomarkers model (Aβ42/P-tau/T-tau) did not improve ability to separate control and AD, or stable and converter aMCI patients. Our results support that elevated CSF NfL could predict progression in aMCI patients, but its utility cannot improve the core AD biomarkers.en_US
dc.language.isoengen_US
dc.publisherElsevier Scienceen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleCSF neurofilament light may predict progression from amnestic mild cognitive impairment to Alzheimer's disease dementiaen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber78-85en_US
dc.source.volume107en_US
dc.source.journalNeurobiology of Agingen_US
dc.identifier.doi10.1016/j.neurobiolaging.2021.07.013
dc.identifier.cristin1930318
dc.description.localcodeThis is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal