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  4. Multicenter Alzheimer's and Parkinson's disease immune biomarker verification study
 
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2020
Journal Article
Title

Multicenter Alzheimer's and Parkinson's disease immune biomarker verification study

Abstract
Introduction: Multiple immunity biomarkers have been suggested as tracers of neuroinflammation in neurodegeneration. This study aimed to verify findings in cerebrospinal fluid (CSF) samples of Alzheimer's disease (AD) and Parkinson's disease (PD) subjects from the network of the European, Innovative Medicines Initiative-funded project AETIONOMY. Methods: A total of 227 samples from the studies/centres AETIONOMY, ICEBERG, and IDIBAPS were used to analyse 21 selected immunity biomarkers in CSF. Results were compared to data of an independent cohort of 399 subjects previously published. Results: Immunity markers were predominantly and reproducibly associated with pathological levels of tau isoforms, but also with amyloid levels, aging, sex, APOE genotype, and center-specific factors. Discussion: Immunity biomarker levels in CSF reflect molecular and cellular pathology rather than diagnosis in neurodegenerative disorders. Assay standardization and stratification for age and other covariates could improve the power of such markers in clinical applications or intervention studies targeting immune responses in neurodegeneration.
Author(s)
Brosseron, Frederic
Kolbe, Carl-Christian
Santarelli, Francesco
Carvalho, Stephanie
Antonell, Anna
Castro-Gomez, Sergio
Tacik, Pawel
Namasivayam, Aishwarya Alex
Mangone, Graziella
Schneider, Reinhard
Latz, Eicke
Wüllner, Ullrich
Svenningsson, Per
Sánchez-Valle, Raquel
Molinuevo, José Luis
Corvol, Jean-Christophe
Heneka, Michael T.
Hofmann-Apitius, Martin  
Springstubbe, Stephan  
Fröhlich, Holger  
et al.
Journal
Alzheimer's & dementia  
Open Access
DOI
10.1016/j.jalz.2019.07.018
File(s)
N-614392.pdf (8.33 MB)
Rights
CC BY-NC-ND 4.0: Creative Commons Attribution-NonCommercial-NoDerivatives
Language
English
Fraunhofer-Institut für Algorithmen und Wissenschaftliches Rechnen SCAI  
Keyword(s)
  • Alzheimer's disease

  • Parkinson's disease

  • mild cognitive impairment

  • cerebrospinal fluid

  • Biomarker

  • inflammation

  • amyloid

  • tau

  • aging

  • multicenter

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