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ABSTRACT: Introduction
This study evaluated whether plasma phosphorylated tau-217 (p-tau217), amyloid beta (Aβ)42/40, and their combination could serve as biomarkers of Aβ co-pathology across the Lewy body continuum, where Aβ is frequently observed from prodromal to symptomatic stages.Methods
Individuals with dementia with Lewy bodies (DLB), Parkinson's disease (PD), and their shared prodromal stage, isolated rapid eye movement (REM) sleep behavior disorder (iRBD) underwent plasma sampling, Aβ-PET, and cognitive testing.Results
Higher plasma p-tau217, lower Aβ42/40, and their interaction were associated with greater Aβ-PET uptake. Individuals with higher-than-median p-tau217 and lower-than-median Aβ42/40 showed the highest Aβ burden. Both biomarkers predicted Aβ-PET positivit
SUBMITTER: Woo KA
PROVIDER: S-EPMC12515049 | biostudies-literature | 2025 Oct
REPOSITORIES: biostudies-literature