Evidence map›Paper›PMID 35568889›Full record

ArticleAlzheimer's research & therapy2022

Diagnostic and prognostic performance to detect Alzheimer's disease and clinical progression of a novel assay for plasma p-tau217.

Colin Groot, Claudia Cicognola, Divya Bali, Gallen Triana-Baltzer, Jeffrey L Dage, Michael J Pontecorvo, Hartmuth C Kolb, Rik Ossenkoppele, Shorena Janelidze, Oskar Hansson

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 84 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 5 pooled it
13.1field-weighted citation impact, top 1% of its field
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

84 citing papers in PubMed, 5 syntheses or guidelines pooled it, 94 citations in OpenAlex.

  1. Pooled it
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  13. Head-to-head comparison of brain-derived pTau217 and total pTau217 for brain amyloid and tau pathology classification.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  20. Enhancing Alzheimer's Diagnosis: Leveraging Anatomical Landmarks in Graph Convolutional Neural Networks on Tetrahedral Meshes.Information processing in medical imaging : proceedings of the ... conference · 2026
    Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 3 countries.

Colin Groot *Clinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden. colin.groot@med.lu.se.
Claudia Cicognola *Clinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden.
Divya BaliClinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden.
Gallen Triana-BaltzerNeuroscience Biomarkers, Janssen Research & Development, La Jolla, CA, USA.
Jeffrey L DageStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Michael J PontecorvoAvid Radiopharmaceuticals, Philadelphia, PA, USA.
Hartmuth C KolbNeuroscience Biomarkers, Janssen Research & Development, La Jolla, CA, USA.
Rik OssenkoppeleClinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden.
Shorena JanelidzeClinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden.
Oskar HanssonClinical Memory Research Unit, Department of Clinical Sciences, Skånes universitetssjukhus, VE Minnessjukdomar, Lund University, 205 02, Malmö, Sweden. oskar.hansson@med.lu.se.
Lund University · SEJanssen (United States) · USSkåne University Hospital · SEAmsterdam University Medical Centers · NLEli Lilly (United States) · USIndiana University School of Medicine

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent advances in disease-modifying treatments highlight the need for accurately identifying individuals in early Alzheimer's disease (AD) stages and for monitoring of treatment effects. Plasma measurements of phosphorylated tau (p-tau) are a promising biomarker for AD, but different assays show varying diagnostic and prognostic accuracies. The objective of this study was to determine the clinical performance of a novel plasma p-tau217 (p-tau217) assay, p-tau217+

resultsBoth assays showed similar performance in detecting amyloid-β status in CSF (plasma p-tau217+

conclusionsTaken together, our results indicate good diagnostic and prognostic performance of the plasma p-tau217+

Indexed as

Alzheimer DiseaseCognitive DysfunctionAmyloid beta-PeptidesBiomarkersDisease ProgressionHumansPrognosistau ProteinsAmyloid beta-PeptidesBiomarkerstau ProteinsAlzheimer’s diseaseAssayMild cognitive impairmentPlasma biomarkersp-tau

Identifiers

PMID35568889
PMCPMC9107269
OpenAlexW4280572081

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.