Evidence map›Paper›PMID 38182740›Full record

ArticleScientific reports2024

Clinical evaluation of a novel plasma pTau217 electrochemiluminescence immunoassay in Alzheimer's disease.

Pia Kivisäkk, Hadia A Fatima, Danielle S Cahoon, Brunah Otieno, Leena Chacko, Farnaz Minooei, Catherine Demos, Martin Stengelin, George Sigal, Jacob Wohlstadter and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
16.7field-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

44 citing papers in PubMed, 51 citations in OpenAlex.

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  9. Biolipid Film-Fused Electrochemiluminescence for Multipurpose In Situ Bioassays.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

11 authors at 2 institutions in 1 country.

Pia KivisäkkAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, 114 16th Street, Room 2300, Charlestown, Boston, MA, 02129, USA. pkivisakk@mgh.harvard.edu.ORCID 0000-0001-9708-7509
Hadia A FatimaAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, 114 16th Street, Room 2300, Charlestown, Boston, MA, 02129, USA.
Danielle S CahoonAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, 114 16th Street, Room 2300, Charlestown, Boston, MA, 02129, USA.
Brunah OtienoMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Leena ChackoMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Farnaz MinooeiMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Catherine DemosMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Martin StengelinMeso Scale Diagnostics, LLC., Rockville, MD, USA.
George SigalMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Jacob WohlstadterMeso Scale Diagnostics, LLC., Rockville, MD, USA.
Steven E ArnoldAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, 114 16th Street, Room 2300, Charlestown, Boston, MA, 02129, USA.
Meso Scale Discovery (United States) · USHarvard University · US

Funding

Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI STEVEN E ARNOLD · 2019 to 2026
$36.5M
NIA NIH HHS P30 AG062421
6 · The paper itself

Abstract

A growing literature suggests that plasma levels of tau phosphorylated at amino acid 217 (pTau217) performs similarly to cerebrospinal fluid (CSF) biomarkers and PET imaging to detect amyloid pathology and to provide diagnostic and prognostic information in Alzheimer's disease (AD), but a significant limiting factor thus far has been a lack of widely available immunoassays. We evaluated a novel pTau217 S-PLEX® assay developed by Meso Scale Discovery (MSD; Rockville, MD) in plasma from 131 individuals with AD confirmed by CSF biomarkers and controls. Technical performance of the assay was excellent with an LLOQ of 1.84 pg/mL and intra/interplate CVs of 5.5% (0.3-15.0%) and 5.7% (range 0.3-13.4%), respectively. The pTau217 plasma assay differentiated AD and controls with an AUC of 0.98 (95% CI 0.96-1.0) and pTau217 levels were 3.9-fold higher in individuals with AD. This performance was significantly better than what was observed for plasma pTau181, performed in parallel, and comparable to published data on existing pTau217 assays. While further clinical validation and head-to-head comparisons are needed to fully establish the role for the novel pTau217 S-PLEX assay, these data demonstrate the utility of the assay to detect AD pathology.

Indexed as

Alzheimer DiseaseAmino AcidsAmyloidogenic ProteinsBiomarkersHumansImmunologic TestsAmino AcidsAmyloidogenic ProteinsBiomarkers

Identifiers

PMID38182740
PMCPMC10770381
OpenAlexW4390617552

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.