Affiliation:
1. Department of Neurology, The Catholic University of Korea Eunpyeong St. Mary’s Hospital, Seoul, Republic of Korea
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 neurofilament
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 evaluations
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 dementia,
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.
Publisher
Bentham Science Publishers Ltd.
Cited by
1 articles.
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