Evidence map›Paper›PMID 42254957›Full record

ArticleInnovation (Cambridge (Mass.))2026

Plasma p-Tau217 improves diagnostic accuracy and clinician confidence in cognitive disorder classification.

Yu-Yuan Huang, Ling-Ling Li, Rui-Xin Yao, Jay Zengjun Dong, Yi-Han Gan, Yi-Lin Chen, Ke-Liang Chen, Shu-Fen Chen, Ming-Yang Yuan, Jia-Wei Xin and 7 more

Abstract read
In one paragraph

Article in Innovation (Cambridge (Mass.)), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Yu-Yuan HuangDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Ling-Ling LiDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Rui-Xin YaoDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Jay Zengjun DongUltraDx Biotechnology (Shanghai) Co., Ltd., Shanghai 201203, China.
Yi-Han GanDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Yi-Lin ChenDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Ke-Liang ChenDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Shu-Fen ChenDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Ming-Yang YuanDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Jia-Wei XinDepartment of Neurology, Fujian Medical University Union Hospital, Fujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, Fujian Medical University, Fuzhou 350001, China.
Jun WangDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, Chongqing 400038, China.
Ya-Ru ZhangDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
YuJing WangUltraDx Biotechnology (Shanghai) Co., Ltd., Shanghai 201203, China.
Tzu-Chen YenAPRINOIA Therapeutics Co., Ltd., Suzhou 215000, China.
Mei CuiDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Yu GuoDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Jin-Tai YuDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Shanghai Academy of Natural Sciences, New Cornerstone Science Laboratory, Shanghai Medical College, Fudan University, Shanghai 200040, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical utility of plasma phosphorylated tau at threonine 217 (p-tau217) levels as a diagnostic tool for cognitive disorders in real-world settings remains uncertain. In this cross-sectional retrospective study, 738 consecutive subjects presenting with cognitive complaints at a memory clinic underwent diagnostic evaluation incorporating plasma p-tau217 alongside standard clinical assessments ("tier 2": routine neuroimaging and cognitive testing) and advanced biomarker testing ("tier 1": amyloid positron emission tomography [PET] imaging or cerebrospinal fluid [CSF] analysis). Diagnostic impact and confidence were assessed using clinician surveys. Incorporating plasma p-tau217 into the routine tier 2 diagnostic workup significantly influenced clinical decision-making, leading to diagnostic revisions in 30.2% of cases and improving overall diagnostic confidence from 65.1% to 79.4%. Plasma p-tau217 demonstrated high diagnostic accuracy for Alzheimer's disease (AD), with a sensitivity of 0.88 and a specificity of 0.84. Notably, its specificity was superior to tier 2 diagnoses, whereas its sensitivity did not differ significantly. Plasma p-tau217 also exhibited non-inferior performance to tier 1 approaches in the diagnostic distribution of AD, though with marginally lower diagnostic confidence. For non-AD diagnoses, plasma p-tau217 significantly impacted the classification of synucleinopathies and performed comparably to tier 1 methods. In conclusion, plasma p-tau217 meaningfully impacted diagnostic precision and confidence in subjects presenting to a real-world memory clinic, offering a minimally invasive, cost-effective, and accessible alternative to state-of-the-art examinations. As the global population ages and cognitive disorders become more prevalent, the integration of plasma p-tau217 into routine practice has the potential to streamline diagnostic workflows and enhance the efficient utilization of medical resources.

Indexed as

Alzheimer’s diseaseblood markerscerebrospinal fluidplasma p-tau217positron emission tomography

Identifiers

PMID42254957
PMCPMC13237847

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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.