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1000 Titel
  • Evaluation of cerebrospinal fluid glycoprotein NMB (GPNMB) as a potential biomarker for Alzheimer’s disease
1000 Autor/in
  1. Aichholzer, Freyja |
  2. Klafki, Hans-Wolfgang |
  3. Ogorek, Isabella |
  4. Vogelgsang, Jonathan |
  5. Wiltfang, Jens |
  6. Scherbaum, Norbert |
  7. Weggen, Sascha |
  8. Wirths, Oliver |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-05-04
1000 Erschienen in
1000 Quellenangabe
  • 13(1):94
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13195-021-00828-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097817/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Alzheimer's disease (AD) is a neurodegenerative disorder associated with extracellular amyloid-β peptide deposition and progressive neuron loss. Strong evidence supports that neuroinflammatory changes such as the activation of astrocytes and microglia cells are important in the disease process. Glycoprotein nonmetastatic melanoma protein B (GPNMB) is a transmembrane glycoprotein that has recently been associated with an emerging role in neuroinflammation, which has been reported to be increased in post-mortem brain samples from AD and Parkinson's disease patients.!##!Methods!#!The present study describes the partial 'fit for purpose' validation of a commercially available immunoassay for the determination of GPNMB levels in the cerebrospinal fluid (CSF). We further assessed the applicability of GPNMB as a potential biomarker for AD in two different cohorts that were defined by biomarker-supported clinical diagnosis or by neuroimaging with amyloid positron emission tomography, respectively.!##!Results!#!The results indicated that CSF GPNMB levels could not distinguish between AD or controls with other neurological diseases but correlated with other parameters such as aging and CSF pTau levels.!##!Conclusions!#!The findings of this study do not support GPNMB in CSF as a valuable neurochemical diagnostic biomarker of AD but warrant further studies employing healthy control individuals.
1000 Sacherschließung
lokal Membrane Glycoproteins [MeSH]
lokal Humans [MeSH]
lokal Inflammation
lokal Amyloid beta-Peptides [MeSH]
lokal Alzheimer Disease/diagnostic imaging [MeSH]
lokal Cerebrospinal fluid
lokal Immunoassay
lokal Peptide Fragments [MeSH]
lokal Biomarker
lokal Alzheimer’s disease
lokal GPNMB
lokal Research
lokal tau Proteins [MeSH]
lokal Glycoproteins [MeSH]
lokal Microglia [MeSH]
lokal Biomarkers [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/QWljaGhvbHplciwgRnJleWph|https://frl.publisso.de/adhoc/uri/S2xhZmtpLCBIYW5zLVdvbGZnYW5n|https://frl.publisso.de/adhoc/uri/T2dvcmVrLCBJc2FiZWxsYQ==|https://frl.publisso.de/adhoc/uri/Vm9nZWxnc2FuZywgSm9uYXRoYW4=|https://frl.publisso.de/adhoc/uri/V2lsdGZhbmcsIEplbnM=|https://frl.publisso.de/adhoc/uri/U2NoZXJiYXVtLCBOb3JiZXJ0|https://frl.publisso.de/adhoc/uri/V2VnZ2VuLCBTYXNjaGE=|https://orcid.org/0000-0002-4115-0334
1000 Hinweis
  • DeepGreen-ID: 6e9625a1e8bf425cb40191bfc28af2df ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 @id frl:6464017.rdf
1000 Erstellt am 2023-11-15T23:36:01.937+0100
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1000 Zuletzt bearbeitet 2023-11-30T22:50:44.414+0100
1000 Objekt bearb. Thu Nov 30 22:50:44 CET 2023
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