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ABSTRACT: Importance
Allelic variation in the brain-derived neurotrophic factor (BDNF) Val66Met polymorphism moderates increases in cerebrospinal fluid (CSF) levels of tau and phosphorylated tau 181 (p-tau181), measured using immunoassay, and cognitive decline in presymptomatic dominantly inherited Alzheimer disease (DIAD). Advances in mass spectrometry show that CSF tau phosphorylation occupancy at threonine 181 and 217 (p-tau181/tau181, p-tau217/tau217) increases with initial β-amyloid (Aβ) aggregation, while phosphorylation occupancy at threonine 205 (p-tau205/tau205) and level of total tau increase when brain atrophy and clinical symptoms become evident.Objective
To determine whether site-specific tau phosphorylation occupancy (ratio of phosphorylated to unphosphorylated tau) is
SUBMITTER: Lim YY
PROVIDER: S-EPMC8804973 | biostudies-literature | 2022 Mar
REPOSITORIES: biostudies-literature