Evidence map›Paper›PMID 41787549›Full record

ArticleAlzheimer's research & therapy2026

Evaluating the real-world performance of plasma pTau217 and pTau181 in a Southeast Asian tertiary memory clinic.

Yi Jayne Tan, Raziyeh Mohammadi, Seyed Ehsan Saffari, Nicole Isabella Tan, Louis Ss Lim, Shermine Hl Low, Louis Cs Tan, Hui Jin Chiew, Kok Pin Ng, Shahul Hameed and 2 more

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yi Jayne TanDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Raziyeh MohammadiCenter for Quantitative Medicine, Duke-NUS Medical School, National University of Singapore, 8 College Road, Singapore, S169857, Singapore.
Seyed Ehsan SaffariDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Nicole Isabella TanDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Louis Ss LimDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Shermine Hl LowDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Louis Cs TanDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Hui Jin ChiewDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Kok Pin NgDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore.
Shahul HameedDepartment of Neurology, National Neuroscience Institute, Singapore General Hospital, Outram Road, Singapore, S169608, Singapore.
Simon Ks TingDepartment of Neurology, National Neuroscience Institute, Singapore General Hospital, Outram Road, Singapore, S169608, Singapore.
Adeline Sl NgDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, S308433, Singapore. adeline.ng.s.l@singhealth.com.sg.

Funding

National Medical Research Council MOH-CNIG22jul-0006National Medical Research Council MOH-CSAINV21-0005, NMRC/CG2/005a/2022-NNINational Medical Research Council MOH-OFLCG18May-0002SingHealth Fund- NNI Fund SHF(U)/22/GC-5C/007(EC), SHF(U)/23/GC-2C/002(EC)
6 · The paper itself

Abstract

backgroundRecent advancements in plasma pTau217 have shown its potential as a reliable biomarker for detecting brain amyloid pathology (Aβ) in Alzheimer’s disease (AD). However, its application in real-world settings remains limited, particularly in non-Caucasian populations such as those in Asia. While plasma pTau217 has demonstrated high accuracy in research cohorts, most studies have been conducted in Western populations. We evaluated the performance of plasma pTau217 and pTau181 with longitudinal cognition in a real-world tertiary memory clinic setting.

methodsPlasma ptau217 was measured using ALZpath SIMOA assay in 291 participants [68 healthy controls (HC), 100 mild cognitive impairment (MCI), 86 AD dementia (ADD), 37 non-AD dementia] from National Neuroscience Institute, Singapore. Performances of pTau217, derived reference ranges (low-, intermediate-, high-) for amyloid positivity and associations with cognitive decline over 4 years was evaluated.

resultsPlasma pTau217 [(area under the curve (AUC) = 0.942)] outperformed pTau181 (AUC = 0.909) in differentiating ADD from other disease groups. Amongst patients with known amyloid status (n = 40), pTau217 identified Aβ + with AUC = 0.961 vs. pTau181 with AUC = 0.917. Using a two cut-point approach, a 95% sensitivity and specificity for Aβ + corresponded to pTau217 > 0.66 pg/ml and < 0.38 pg/ml, respectively. With these two cut-points, patients in the total cohort were stratified into low-, intermediate-, and high-risk groups for Aβ + . The high-risk group exhibited the steepest annual decline in both MoCA (-2.382) and MMSE (-1.580) scores; while the low-risk group demonstrated relatively stable cognitive performance over time. By applying a k-means clustering analysis, we identified three clusters of participants representing stable, slow, and fast progressors. Fast progressors exhibit the most pronounced cognitive decline and the highest pTau217 levels. DISCUSSION: Plasma pTau217 demonstrates high diagnostic accuracy and effectively predicts cognitive decline even in individuals without known Aβ + status, potentially reducing reliance on amyloid PET confirmation. Our findings reinforce the clinical utility of plasma pTau217 as a prognostic biomarker for AD progression, offering a practical, non-invasive tool for assessing cognitive decline in real-world Southeast Asian memory clinics.

Indexed as

Alzheimer DiseaseCognitive DysfunctionPeptide Fragmentstau ProteinsAgedAmyloid beta-PeptidesBiomarkersFemaleHumansMaleMiddle AgedNeuropsychological TestsSingaporeTertiary Care CentersAmyloid beta-PeptidesBiomarkersMAPT protein, humanPeptide Fragmentstau ProteinsAlzheimer’s diseaseBlood biomarkerscut-offsPlasma phosphorylated tau217Simoa ALZpath

Identifiers

PMID41787549
PMCPMC13069703

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.