The effect of lumbar puncture on the neurodegeneration biomarker neurofilament light in macaque monkeys.

amyloid beta biomarkers cerebrospinal fluid cisterna magna puncture lumbar puncture neurofilament light non‐human primate models tau

Journal

Alzheimer's & dementia (Amsterdam, Netherlands)
ISSN: 2352-8729
Titre abrégé: Alzheimers Dement (Amst)
Pays: United States
ID NLM: 101654604

Informations de publication

Date de publication:
2020
Historique:
received: 03 04 2020
revised: 20 06 2020
accepted: 22 06 2020
entrez: 23 7 2020
pubmed: 23 7 2020
medline: 23 7 2020
Statut: epublish

Résumé

Neurofilament light (NFL) in cerebrospinal fluid (CSF) is elevated in neurodegenerative disease patients, and may track disease progression and treatment. Macaque monkeys are emerging as important translational models of neurodegeneration, and NFL may be a useful biomarker. To determine the influence of a previous lumbar puncture (LP) on NFL, we collected CSF at multiple time points in macaque monkeys via LP or cisterna magna puncture. NFL, amyloid beta (Aβ40, Aβ42), and tau (tTau, pTau) in CSF were measured by standard enzyme-linked immunosorbent assay and multiplex. NFL was significantly elevated at 14 to 23 days after an LP (median increase: 162%). Aβ and tau biomarkers remained stable. NFL peaked and decayed over 1 to 2 months after LP. NFL was not elevated after cisterna magna puncture. Results suggest damage of the cauda equina during LP may increase NFL. Caution should be taken in interpreting NFL concentration in studies in which repeat LPs are performed.

Identifiants

pubmed: 32695873
doi: 10.1002/dad2.12069
pii: DAD212069
pmc: PMC7366296
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12069

Informations de copyright

© 2020 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, Inc. on behalf of Alzheimer's Association.

Déclaration de conflit d'intérêts

The authors have no financial disclosures to declare.

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Auteurs

Susan E Boehnke (SE)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.
Department of Biomedical and Molecular Sciences Queen's University Kingston Ontario Canada.

Emma L Robertson (EL)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.

Brittney Armitage-Brown (B)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.

Robert G Wither (RG)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.

Natalia M Lyra E Silva (NM)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.

Andrew Winterborn (A)

Animal Care Services Queen's University Kingston Ontario Canada.

Ron Levy (R)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.
Department of Surgery Kingston General Hospital Kingston Ontario Canada.

Douglas J Cook (DJ)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.
Department of Surgery Kingston General Hospital Kingston Ontario Canada.

Fernanda G De Felice (FG)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.
Department of Psychiatry Providence Care Hospital Kingston Ontario Canada.
Institute of Medical Biochemistry Leopoldo de Meis Federal University of Rio de Janeiro Rio de Janeiro Brazil.

Douglas P Munoz (DP)

Centre for Neuroscience Studies Queen's University Kingston Ontario Canada.
Department of Biomedical and Molecular Sciences Queen's University Kingston Ontario Canada.

Classifications MeSH