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A high cerebrospinal fluid soluble TREM2 level is associated with slow clinical progression of Alzheimer's disease.
Edwin, Trine Holt; Henjum, Kristi; Nilsson, Lars N G; Watne, Leiv Otto; Persson, Karin; Eldholm, Rannveig Sakshaug; Saltvedt, Ingvild; Halaas, Nathalie Bodd; Selbæk, Geir; Engedal, Knut; Strand, Bjørn Heine; Knapskog, Anne-Brita.
Afiliação
  • Edwin TH; Department of Dementia Research Norwegian National Advisory Unit on Ageing and Health Vestfold Hospital Trust Tønsberg Norway.
  • Henjum K; Department of Geriatric Medicine Oslo University Hospital Oslo Norway.
  • Nilsson LNG; Institute of Clinical Medicine and Institute of Health and Society Faculty of Medicine University of Oslo Oslo Norway.
  • Watne LO; Department of Geriatric Medicine Oslo University Hospital Oslo Norway.
  • Persson K; Department of Pharmacology University of Oslo and Oslo University Hospital Oslo Norway.
  • Eldholm RS; Department of Geriatric Medicine Oslo Delirium Research Group Oslo University Hospital Oslo Norway.
  • Saltvedt I; Department of Pharmacology University of Oslo and Oslo University Hospital Oslo Norway.
  • Halaas NB; Department of Geriatric Medicine Oslo University Hospital Oslo Norway.
  • Selbæk G; Department of Geriatric Medicine Oslo Delirium Research Group Oslo University Hospital Oslo Norway.
  • Engedal K; Department of Dementia Research Norwegian National Advisory Unit on Ageing and Health Vestfold Hospital Trust Tønsberg Norway.
  • Strand BH; Department of Geriatric Medicine Oslo University Hospital Oslo Norway.
  • Knapskog AB; Department of Neuromedicine and Movement Science Norwegian University of Science and Technology Trondheim Norway.
Alzheimers Dement (Amst) ; 12(1): e12128, 2020.
Article em En | MEDLINE | ID: mdl-33313376
ABSTRACT

INTRODUCTION:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2020 Tipo de documento: Article