Evidence map›Paper›PMID 41610380›Full record

ArticleNeurology2026

Postmortem Associations Between Alzheimer Disease Pathology and Plasma pTau217, GFAP, and NfL in AD and AD-Related Dementias.

Pia Kivisäkk, Hadia Fatima, Chao-Yi Wu, Nikhil Padmanabhan, Daniel Romero, Taron Gorham, Molly Weik, Hiroko H Dodge, Clemens R Scherzer, Sudeshna Das and 11 more

Abstract read
In one paragraph

Article in Neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

21 authors.

Pia KivisäkkAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0001-9708-7509
Hadia FatimaAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Chao-Yi WuAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0002-2187-6509
Nikhil PadmanabhanMeso Scale Diagnostics, LLC., Rockville, MD.
Daniel RomeroMeso Scale Diagnostics, LLC., Rockville, MD.
Taron GorhamMeso Scale Diagnostics, LLC., Rockville, MD.
Molly WeikAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Hiroko H DodgeAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0001-7290-8307
Clemens R ScherzerStephen & Denise Adams Center for Parkinson's Disease Research, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-0567-9193
Sudeshna DasMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.
Lori B ChibnikMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.ORCID 0000-0001-6293-806X
Deborah L BlackerMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.ORCID 0000-0001-6107-7376
Teresa Gomez-IslaMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.
Derek H OakleyMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.ORCID 0000-0002-6998-9510
Matthew P FroschMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.
Bradley T HymanMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.ORCID 0000-0002-7959-9401
Catherine DemosMeso Scale Diagnostics, LLC., Rockville, MD.
George SigalMeso Scale Diagnostics, LLC., Rockville, MD.
Jacob N WohlstadterMeso Scale Diagnostics, LLC., Rockville, MD.
Alberto Serrano-PozoMassachusetts Alzheimer's Disease Research Center, Charlestown, MA.ORCID 0000-0003-0899-7530
Steven E ArnoldAlzheimer's Clinical and Translational Research Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0002-9487-415X

Funding

Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Christine S Ritchie · 2019 to 2026
$36.5M
Genome-Wide Prediction of Dementia in Parkinson's DiseaseR01NS115144 · NINDS · YALE UNIVERSITY · PI SCHERZER, CLEMENS R · 2019 to 2025
$4.4M
NIA NIH HHS P30 AG062421NINDS NIH HHS R01 NS115144
6 · The paper itself

Abstract

BACKGROUND AND

objectivesAlzheimer disease (AD) and its related disorders (ADRDs) are characterized by a high frequency of copathologies. We aimed to determine the specificity of plasma pTau217, glial fibrillary acidic protein (GFAP), and neurofilament light chain (NfL) for AD neuropathological change (ADNC) in the presence of common ADRD copathologies.

methodspTau217, GFAP, and NfL were measured using S-PLEX immunoassays from Meso Scale Discovery in banked plasma samples from 2 groups of participants in the Massachusetts Alzheimer's Disease Research Center (MADRC) Longitudinal Cohort study: (1) participants spanning the cognitive spectrum, who underwent brain autopsy, and blood collection within 6 years before death, and (2) participants with normal cognition and no neurologic diagnosis during 5 years of follow-up, but no autopsy data (normal controls [NCs]). Cross-sectional associations between biomarker levels and ADNC, primary neuropathologic diagnosis (NPDx1), and presence of non-AD copathologies were evaluated using linear regression models controlling for age, sex, and time to death.

resultsOne hundred eighty-seven participants with brain autopsy (NPDx1: AD n = 85; other n = 102; mean age: 74.3 years, 38.5% female; interval blood collection-death [mean ± SD]: 2.8 ± 1.6 years) and 67 NC without brain autopsy (mean age: 66.5 years, 71.6% female) were included. pTau217, but not GFAP, levels increased stepwise with increasing Thal phases (β = 0.61; 95% CI [0.24-0.97] to β = 0.91 [0.55-1.27]) and Braak stages (β = 0.59; [0.16-1.01] to β = 0.74 [0.33-1.15]). Although 23% of individuals with a non-AD NPDx1 had increased pTau217 levels using a cutoff defined by the contrast between ADNC and NC, the majority (62%) had intermediate/high ADNC copathology and the remaining pTau217+ individuals had borderline increased levels. By contrast, 48% of individuals without ADNC had increased GFAP levels. pTau217 and GFAP were not different in the presence or absence of cerebral amyloid angiopathy, α-synuclein or TDP-43 proteinopathies, or primary tauopathies. NfL was not specifically associated with ADNC. DISCUSSION: Plasma pTau217, but not GFAP or NfL, levels accurately reflect the presence of ADNC in the brain even in individuals with an NPDx1 of a non-AD dementia. Thus, a positive plasma pTau217 test in an individual with a suspected non-AD dementia should not necessarily be considered a misdiagnosis of the presumed non-AD dementia or as a false positive, but rather as evidence of ADNC copathology.

Indexed as

Alzheimer DiseaseGlial Fibrillary Acidic ProteinNeurofilament Proteinstau ProteinsAgedAged, 80 and overAutopsyBiomarkersBrainCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament Proteinstau Proteins

Identifiers

PMID41610380
PMCPMC12857747

What Socratic holds

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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.