Cited by 25Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

Liquid biopsy of cerebrospinal fluid identifies neuronal pentraxin receptor (NPTXR) as a biomarker of progression of Alzheimer’s disease

Lim, Bryant, Tsolaki, Magda, Soosaipillai, Antoninus, Brown, Marshall, Zilakaki, Maria, Tagaraki, Fani, Fotiou, Dimitrios, Koutsouraki, Effrosyni +3 more·2019·Clinical Chemistry and Laboratory Medicine (CCLM)

Abstract

Background Alzheimer's disease (AD) is the most prevalent form of dementia. Currently, the most studied biomarkers of AD are cerebrospinal fluid (CSF) amyloid β 1-42, total tau and phosphorylated tau. However, misdiagnosis can exceed 20%. Recently, we found that CSF amyloid β precursor-like protein-1 (APLP1) and neuronal pentraxin receptor (NPTXR) are promising biomarkers of AD. The aim of the present study is to validate CSF APLP1 and NPTXR as biomarkers of AD severity. Methods APLP1 and NPTXR concentrations were measured in the CSF of patients with mild cognitive impairment (MCI) (n = 14), mild AD (n = 21), moderate AD (n = 43) and severe AD (n = 30) using enzyme-linked immunosorbent assays (ELISAs). Results CSF APLP1 and NPTXR were not associated with age or sex. CSF APLP1 was not different between any of the AD severity groups (p = 0.31). CSF NPTXR was significantly different between MCI and mild AD (p = 0.006), mild and moderate AD (p = 0.016), but not between moderate and severe AD (p = 0.36). NPTXR concentration progressively declined from MCI to mild, to moderate and to severe AD patients (p < 0.0001, Kruskal-Wallis test). CSF NPTXR positively correlated with the Mini-Mental Status Examination (MMSE) score (p < 0.001). Conclusions NPTXR concentration in CSF is a promising biomarker of AD severity and could inform treatment success and disease progression in clinical settings.

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Crossref · 10.1515/cclm-2019-0428

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Authors
Lim, B., Tsolaki, M., Soosaipillai, A., Brown, M., Zilakaki, M., Tagaraki, F., Fotiou, D., Koutsouraki, E., Grosi, E., Prassas, I., & Diamandis, E. P.
Affiliations
  • University of Toronto (CA)
  • Aristotle University of Thessaloniki (GR)
  • Mount Sinai Hospital (CA)
  • Fred Hutch Cancer Center (US)
  • 1st Department of Neurology, Medical School , Aristotle University of Thessaloniki , Thessaloniki , Greece
Corresponding author
  • Tsolaki, Magda
  • Diamandis, Eleftherios P.
Venue
Clinical Chemistry and Laboratory Medicine (CCLM)
Published
2019-08-15
Volume
57
Issue
12
Pages
1875-1881
ISSN
  • 1434-6621 (ISSN-L)
  • 1437-4331
OpenAlex
W2968734721
Cited by
25
References
29
Citations by year
2026: 1 · 2025: 3 · 2024: 3 · 2023: 5 · 2022: 5 · 2021: 2 · 2020: 6
FWCI
2.58
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Chemistry and Laboratory Medicine (CCLM) (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
Keywords
Alzheimer's disease, liquid biopsy, cerebrospinal fluid biomarkers, disease progression, mild cognitive impairment, disease severity, Mini-Mental State Examination
MeSH terms
Liquid Biopsy, Pentraxins, Aged, Alzheimer Disease, C-Reactive Protein, Female, Greece, Humans, Male, Middle Aged, Nerve Tissue Proteins, Peptide Fragments, Biomarkers, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, tau Proteins, Disease Progression, Cognitive Dysfunction

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