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dc.contributor.authorIdland, Ane-Victoria
dc.contributor.authorRoser, Sala-Llonch
dc.contributor.authorBorza, Tom
dc.contributor.authorWatne, Leiv Otto
dc.contributor.authorWyller, Torgeir Bruun
dc.contributor.authorBrækhus, Anne
dc.contributor.authorZetterberg, Henrik
dc.contributor.authorBlennow, Kaj
dc.contributor.authorWalhovd, Kristine B
dc.contributor.authorFjell, Anders Martin
dc.date.accessioned2018-10-10T13:17:53Z
dc.date.available2018-10-10T13:17:53Z
dc.date.created2016-11-07T08:56:09Z
dc.date.issued2017
dc.identifier.citationNeurobiology of Aging. 2017, 49 138-144.nb_NO
dc.identifier.issn0197-4580
dc.identifier.urihttp://hdl.handle.net/11250/2567476
dc.description.abstractCerebrospinal fluid (CSF) neurofilament light (NFL) is a marker of axonal degeneration. We tested whether CSF NFL levels predict hippocampal atrophy rate in cognitively healthy older adults independently of the established CSF Alzheimer's disease (AD) biomarkers, β-amyloid 1-42, and phosphorylated tau (P-tau). We included 144 participants in a 2-year longitudinal study with baseline CSF measures and 2 magnetic resonance images. Eighty-eight participants had full data available. A subgroup of 36 participants with very low AD risk was also studied. NFL predicted hippocampal atrophy rate independently of age, β-amyloid 1-42, and P-tau. Including NFL, P-tau, and age in the same model, higher NFL and lower P-tau predicted higher hippocampal atrophy (R2 = 0.20, NFL: β = -0.34; p = 0.003; P-tau: β = 0.27; p = 0.009). The results were upheld in the participants with very low AD risk. NFL predicted neurodegeneration in older adults with very low AD probability. We suggest that factors previously shown to be important for brain degeneration in mild cognitive impairment may also impact changes in normal aging, demonstrating that NFL is likely to indicate AD-independent, age-expected neurodegeneration.nb_NO
dc.description.sponsorshipThe study was mainly funded by the Medical Student Research Program at the University of Oslo and The National Association for Public Health’s dementia research program, Norway. Further, we have received funding from Innlandet Hospital Trust, the Knut and Alice Wallenberg Foundation, the Swedish Research Council, and the Torsten Söderberg Foundation at the Royal Swedish Academy of Sciences.nb_NO
dc.language.isoengnb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.subjectCerebrospinal fluid;nb_NO
dc.subjectHippocampal atrophy rate;nb_NO
dc.subjectMagnetic resonance imaging;nb_NO
dc.subjectNeurofilament light;nb_NO
dc.subjectNormal aging;nb_NO
dc.titleCSF neurofilament light levels predict hippocampal atrophy in cognitively healthy older adultsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.rights.holderDette verket har følgende lisens: Attribution-NonCommercial-NoDerivatives 4.0 Internationalnb_NO
dc.source.pagenumber138-144nb_NO
dc.source.volume49nb_NO
dc.source.journalNeurobiology of Agingnb_NO
dc.identifier.doi10.1016/j.neurobiolaging.2016.09.012
dc.identifier.cristin1397850
cristin.unitcode1991,9,0,0
cristin.unitnameDiv Psykisk helsevern
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextpostprint
cristin.qualitycode1


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