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Related Experiment Video

Updated: Jul 12, 2026

In Vitro Aggregation Assays Using Hyperphosphorylated Tau Protein
09:22

In Vitro Aggregation Assays Using Hyperphosphorylated Tau Protein

Published on: January 2, 2015

Prognostic value of plasma brain-derived pTau.

Valentina Ghisays1, Marisa N Denkinger2, Alpana Singh2

  • 1Banner Alzheimer's Institute, Phoenix, AZ, USA.

Medrxiv : the Preprint Server for Health Sciences
|July 10, 2026
PubMed
Summary

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Plasma brain-derived pTau217 (BD-pTau217) shows promise for predicting Alzheimer's disease progression. BD-pTau217 better predicts amyloid PET positivity in early stages than total pTau217.

Area of Science:

  • Neurodegenerative diseases
  • Biomarker discovery
  • Alzheimer's disease research

Background:

  • Plasma biomarkers are crucial for Alzheimer's disease (AD) diagnosis and prognosis.
  • Brain-derived pTau217 (BD-pTau217) may offer greater AD specificity than total pTau217.
  • The prognostic value of BD-pTau217 for predicting clinical and amyloid progression remains unclear.

Purpose of the Study:

  • To compare the prognostic value of BD-pTau217 versus total plasma pTau217.
  • To assess their ability to predict clinical and amyloid PET progression in cognitively unimpaired (CU) individuals.
  • To evaluate biomarker performance in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort.

Main Methods:

  • Utilized plasma biomarker data from 1,427 ADNI participants, including 529 CU individuals.
Keywords:
Alzheimer’s disease progressionBrain-derived pTau217amyloid PET progressionplasma biomarkersplasma phosphorylated tau

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Last Updated: Jul 12, 2026

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Published on: January 2, 2015

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  • Assessed amyloid PET progression in baseline CU amyloid-negative participants using longitudinal PET imaging.
  • Employed Cox models and time-dependent AUC to evaluate associations between biomarkers and progression.
  • Main Results:

    • BD-pTau217 did not significantly outperform total pTau217 in predicting progression to mild cognitive impairment or dementia.
    • However, BD-pTau217 demonstrated superior prediction of amyloid PET positivity at 2.5 and 4 years in amyloid-negative participants (tdAUC 0.82 vs 0.69 and 0.77 vs 0.64, respectively).
    • Hazard ratios indicated a significantly higher risk of progression with elevated BD-pTau217.

    Conclusions:

    • BD-pTau217 enhances the prediction of near-term amyloid PET progression in cognitively unimpaired individuals.
    • The advantage of BD-pTau217 for predicting clinical progression is less pronounced.
    • Plasma BD-pTau217 shows potential as a sensitive biomarker for early AD-related changes.