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Effects of age, amyloid, sex, and APOE ε4 on the CSF proteome in normal cognition
Alzheimer Center Amsterdam, Department of Neurology, Amsterdam, the Netherlands; Neuroscience, Amsterdam UMC Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Clinical Neurochemistry Lab, Institute of Neuroscience and Physiology, Sahlgrenska University Hospital, Mölndal, Sweden; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Mölndal, Sweden.
Nivel, the Netherlands.
Alzheimer Center Limburg, School for Mental Health and Neuroscience, Maastricht University, Maastricht, the Netherlands.
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2022 (English)In: Alzheimer's & dementia (Amsterdam, Netherlands), E-ISSN 2352-8729, Vol. 14, no 1, article id e12286Article in journal (Refereed) Published
Abstract [en]

Introduction: It is important to understand which biological processes change with aging, and how such changes are associated with increased Alzheimer's disease (AD) risk. We studied how cerebrospinal fluid (CSF) proteomics changed with age and tested if associations depended on amyloid status, sex, and apolipoprotein E Ɛ4 genotype.

Methods: We included 277 cognitively intact individuals aged 46 to 89 years from Alzheimer's Disease Neuroimaging Initiative, European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery, and Metabolic Syndrome in Men. In total, 1149 proteins were measured with liquid chromatography mass spectrometry with multiple reaction monitoring/Rules-Based Medicine, tandem mass tag mass spectrometry, and SOMAscan. We tested associations between age and protein levels in linear models and tested enrichment for Reactome pathways.

Results: Levels of 252 proteins increased with age independently of amyloid status. These proteins were associated with immune and signaling processes. Levels of 21 proteins decreased with older age exclusively in amyloid abnormal participants and these were enriched for extracellular matrix organization.

Discussion: We found amyloid-independent and -dependent CSF proteome changes with older age, perhaps representing physiological aging and early AD pathology.

Place, publisher, year, edition, pages
John Wiley & Sons, 2022. Vol. 14, no 1, article id e12286
National Category
Neurosciences
Identifiers
URN: urn:nbn:se:oru:diva-99029DOI: 10.1002/dad2.12286ISI: 000791447400001PubMedID: 35571963Scopus ID: 2-s2.0-85137030832OAI: oai:DiVA.org:oru-99029DiVA, id: diva2:1658624
Funder
Swedish Research Council, 2018-02532European Commission, 681712EU, European Research Council
Note

Funding Agencies:

ZonMW Memorabel grant programme 733050824

Innovative Medicines Initiative Joint Undertaking under EMIF-AD MBD grant 115372

Swedish State Support for Clinical Research

Available from: 2022-05-17 Created: 2022-05-17 Last updated: 2023-03-15Bibliographically approved

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Freund-Levi, Yvonne

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