Liquid biopsy of cerebrospinal fluid identifies neuronal pentraxin receptor (NPTXR) as a biomarker of progression of Alzheimer’s disease
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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CSF NPTXR can discriminate between advanced AD stages and MCI (Area under the curve = 0.799).
“Accordingly, CSF NPTXR can discriminate between advanced AD stages and MCI (Area under the curve = 0.799) (Begcevic et al. 2018; Lim et al. 2019).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Lim et al. 2019
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Self-citation
- 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.
- ORCID
- Venue
- Clinical Chemistry and Laboratory Medicine (CCLM)
- Publisher
- Walter de Gruyter GmbH
- 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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