With emerging amyloid therapies, documentation of the patient's amyloid status to confirm the etiology of a clinical diagnosis is warranted prior to instituting amyloid-based therapy. The Multimer Detection System-Oligomeric Amyloid- (MDS-OA) is a noninvasive blood-based biomarker utilized to measure A oligomerization tendency. We determined the difference in MDS-OA ratio across the groups: (a) no cognitive impairment or subjective cognitive impairment (NCI/SCI), (b) Alzheimer's disease (AD), (c) non-AD, and (d) mixed Alzheimer's disease-Vascular dementia (AD-VaD). MDS-OA level was not significantly different between AD and mixed AD-VaD, but both groups were significantly different from the NCI/SCI and from the non-AD group. An MDS-OA level of >1 could potentially indicate clinical variants of AD or mixed pathology (AD-VaD).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085320PMC
http://dx.doi.org/10.1155/2022/9960832DOI Listing

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