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dc.contributor.authorEdwin, Trine Holt
dc.contributor.authorHenjum, Kristi
dc.contributor.authorNilsson, Lars N. G.
dc.contributor.authorWatne, Leiv
dc.contributor.authorPersson, Karin Ester Torun
dc.contributor.authorEldholm, Rannveig Sakshaug
dc.contributor.authorSaltvedt, Ingvild
dc.contributor.authorHalaas, Nathalie Bodd
dc.contributor.authorSelbæk, Geir
dc.contributor.authorEngedal, Knut
dc.contributor.authorStrand, Bjørn Heine
dc.contributor.authorKnapskog, Anne Brita
dc.date.accessioned2023-05-08T10:11:12Z
dc.date.available2023-05-08T10:11:12Z
dc.date.created2020-12-23T11:57:36Z
dc.date.issued2020
dc.identifier.issn1552-5260
dc.identifier.urihttps://hdl.handle.net/11250/3066793
dc.description.abstractIntroduction: The progression rate of Alzheimer's disease (AD) varies and might be affected by the triggering receptor expressed on myeloid cells (TREM2) activity. We explored if cerebrospinal fluid (CSF) soluble TREM2 (sTREM2), a proxy of microglial activity, is associated with clinical progression rate. Methods: Patients with clinical AD (N = 231) were followed for up to 3 years after diagnosis. Cognitively healthy controls (N = 42) were followed for 5 years. CSF sTREM2 was analyzed by enzyme-linked immunosorbent assay. Group-based trajectory modeling revealed distinct clinical progression groups. Results: Higher CSF sTREM2 was associated with slow clinical progression. The slow- and medium-progressing groups had higher CSF sTREM2 than the cognitively healthy, who had a similar level to patients with rapid clinical progression. Discussion: CSF sTREM2 levels were associated with clinical progression in AD, regardless of core biomarkers. This could be useful in assessing disease development in relation to patient care and clinical trial recruitment. Keywords: Alzheimer's disease; Clinical Dementia Rating scale; disease progression; soluble triggering receptor expressed on myeloid cells 2 (sTREM2); trajectories.
dc.language.isoeng
dc.titleA high cerebrospinal fluid soluble TREM2 level is associated with slow clinical progression of Alzheimer's disease
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.volume12
dc.source.journalAlzheimer's & Dementia
dc.identifier.doi10.1002/dad2.12128
dc.identifier.cristin1863059
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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