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Follow-up Comparisons of Two Plasma Biomarkers of Alzheimer’s Disease, Neurofilament Light Chain, and Oligomeric Aβ: A Pilot Study

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    5 Scopus citations

    Abstract

    Background and Objective: Recent evidence suggests that blood-based biomarkers might be useful for Alzheimer’s disease (AD). Among them, we intend to investigate whether neu-rofilament light (NfL) and multimer detection system-oligomeric Aβ (MDS-OAβ) values can be useful in screening, predicting, and monitoring disease progression and how the relationship between NfL and MDS-OAβ values changes. Methods: Eighty participants with probable AD dementia, 50 with mild cognitive impairment (MCI), and 19 with subjective cognitive decline (SCD) underwent baseline and follow-up evalua-tions of the Mini-Mental Status Examination (MMSE) and both plasma biomarkers. Results: Baseline MDS-OAß (p = 0.016) and NfL (p = 0.002) plasma concentrations differed significantly among groups, but only NfL correlated with baseline MMSE scores (r =-0.278, p = 0.001). In follow-up, neither correlated with MMSE changes overall. However, in SCD and MCI participants (n = 32), baseline MDS-OAß correlated with follow-up MMSE scores (r = 0.532, p = 0.041). Linear regression revealed a relationship between baseline MDS-OAβ and follow-up MMSE scores. In SCD and MCI participants, plasma NfL changes correlated with MMSE changes (r = 0.564, p = 0.028). Conclusion: This study shows that only in participants with SCD and MCI, not including AD de-mentia, can MDS-OAß predict the longitudinal cognitive decline measured by follow-up MMSE. Changes of NfL, not MDS-OAß, parallel the changes of MMSE. Further studies with larger samples and longer durations could strengthen these results.

    Original languageEnglish
    Pages (from-to)715-724
    Number of pages10
    JournalCurrent Alzheimer Research
    Volume20
    Issue number10
    DOIs
    StatePublished - 2023

    Bibliographical note

    Publisher Copyright:
    © 2023 The Author(s).

    Keywords

    • Alzheimer’s disease
    • biomarker
    • mild cognitive impairment
    • multimer detection system-oligomeric Aβ
    • neurofilament light protein
    • plasma

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