Evidence map›Paper›PMID 40610281›Full record

ArticleThe journal of prevention of Alzheimer's disease2025

A modelling approach to derive population-specific cutoff for plasma p-Tau217.

Tau Ming Liew, Alzheimer's Disease Neuroimaging Initiative

Abstract read
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Article in The journal of prevention of Alzheimer's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Tau Ming LiewDepartment of Psychiatry, Singapore General Hospital, Outram Road, Singapore 169608; SingHealth Duke-NUS Medicine Academic Clinical Programme, Duke-NUS Medical School, 8 College Road, Singapore 169857; Health Services and Systems Research, Duke-NUS Medical School, 8 College Road, Singapore 169857; Saw Swee Hock School of Public Health, National University of Singapore, 12 Science Drive 2,#10-01, Singapore 117549. Electronic address: liew.tau.ming@singhealth.com.sg.
Alzheimer's Disease Neuroimaging Initiative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma pTau-217 shows promise for detecting Alzheimer's disease, but needs population-specific cutoffs for effective use. Conventional cutoff determination relies on invasive or costly gold-standards, limiting scalability. This study evaluated Finite Mixture Modelling (FMM) for establishing cutoffs without gold-standards. FMM was applied to derive cutoffs for Lumipulse plasma p-Tau217 and p-Tau217/Aβ42 ratio among 1039 ADNI participants, with validation conducted in a subset with amyloid PET data (n = 711). Additionally, simulations were conducted to determine the minimum sample size for reliable FMM estimation. The results showed that FMM-derived cutoffs effectively classified participants into brain amyloid-negative, -positive, and -indeterminate groups, with an indeterminate proportion <20 %, negative and positive predictive values near or above 90 %, and with p-Tau217/Aβ42 outperforming p-Tau217. These FMM-derived cutoffs demonstrated test performance that surpassed several previously-established cutoffs, including the recent FDA-approved cutoff. At least 900 samples were needed for reliable cutoff estimation. In conclusion, this study demonstrated the effectiveness of a modelling approach for estimating plasma p-Tau217 cutoffs without reliance on gold-standards. This approach simplifies the determinating of population-specific cutoffs and facilitates adoption of plasma p-Tau217 in communities lacking access to gold-standards, including some LMICs.

Indexed as

Alzheimer Diseasetau ProteinsAgedAged, 80 and overAmyloid beta-PeptidesBiomarkersFemaleHumansMalePeptide FragmentsPositron-Emission TomographyAmyloid beta-PeptidesBiomarkersMAPT protein, humanPeptide Fragmentstau ProteinsAlzheimer’s diseaseLower- and middle-income countriesOptimal cutoffPlasma biomarkersp-Tau217/Aβ42 ratio

Identifiers

PMID40610281
PMCPMC12413718

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.