Evidence map›Paper›PMID 40791093›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Plasma tau biomarkers are distinctly associated with tau tangles and decreased with Lewy body pathology.

Laia Montoliu-Gaya, Elizabeth Valeriano-Lorenzo, Nicholas J Ashton, Francisco J López-González, Juan Lantero-Rodriguez, Alicia Ruiz-González, Ana Belén Pastor, Belen Frades, María Ascensión Zea-Sevilla, Meritxell Valentí and 11 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Plasma P-tau217 for detecting amyloid clearance after donanemab in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Trial
  2. Post mortem MRI of cholinergic white matter pathways across neurodegenerative diseases.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  3. Article
  4. Article
  5. Analytical and clinical validation of the Lumipulse G plasma p-tau217 assay for clinical implementation.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  6. Article
  7. Article
  8. Plasma tau biomarkers are distinctly associated with tau tangles and decreased with Lewy body pathology.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    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.

Laia Montoliu-GayaDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.ORCID 0000-0001-7684-6318
Elizabeth Valeriano-LorenzoReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Nicholas J AshtonDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Francisco J López-GonzálezReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Juan Lantero-RodriguezDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Alicia Ruiz-GonzálezReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Ana Belén PastorReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Belen FradesReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
María Ascensión Zea-SevillaReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Meritxell ValentíReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Paloma Ruiz-ValderreyReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Laura SaizReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Iván Burgueño-GarcíaReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Maria José López-MartínezReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Teodoro Del SerReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Gunnar BrinkmalmDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Alberto RábanoReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.
Johan GobomDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Kaj BlennowDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Pascual Sánchez-JuanReina Sofia Foundation Alzheimer Center, CIEN Foundation, ISCIII, Madrid, Spain.

Funding

The effects of iron on oxidative stress and Alzheimer's biomarkers in amyloid-positive and negative elderly normalR01AG068398 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHIANG, GLORIA CHIA-YI · 2020 to 2024
$2.8M
AD Strategic Fund and the Alzheimer's Association #ADSF-21-831376-CAD Strategic Fund and the Alzheimer's Association #ADSF-21-831377-CAD Strategic Fund and the Alzheimer's Association #ADSF-21-831381-CAD Strategic Fund and the Alzheimer's Association #ADSF-24-1284328-CÅhlén-stifelsenAlzheimer Drug Discovery Foundation #RDAPB-201809-2016615Alzheimerfonden AF-968621Alzheimer's Association 2021 Zenith Award ZEN-21-848495Bluefield ProjectBrightfocus Foundation A2022015FCare Research University College London Hospitals Biomedical Research CentreCure Alzheimer's FundErling-Persson Family FoundationEuropean Union Joint Program for Neurodegenerative Disorders JPND2019-466-236European Union Joint Programme - Neurodegenerative Disease Research JPND2021-00694Familjen Rönströms StiftelseGamla Tjänarinnor FoundationGun and Bertil Stohnes FoundationHjärnfonden, Sweden #FO2017-0243Hjärnfonden, Sweden #FO2022-0270NEuroBioStand #22HLT07NIA NIH HHS R01 AG068398NIH HHS #1R01AG068398-01Olav Thon FoundationQueen Sofia FoundationStiftelsen för Gamla TjänarinnorSwedish Alzheimer Foundation #AF-742881Swedish Dementia FoundationSwedish Research Council #2017-00915Swedish State Support for Clinical Research #ALFGBG-71320UK Dementia Research Institute at UCL UKDRI-1003
6 · The paper itself

Abstract

introductionPlasma-to-autopsy studies are essential to understand how tau blood biomarkers change in relation to Alzheimer's disease (AD) brain pathology and how they are influenced by brain co-pathologies and comorbidities.

methodsPlasma samples from 102 brain donors of the Vallecas Alzheimer Reina Sofia cohort were analyzed using a mass spectrometry method to measure the levels of six phosphorylated and two non-phosphorylated tau biomarkers.

resultsIn cases with high pathological burden of AD, phosphorylated tau (p-tau)217 showed associations with neurofibrillary tangle counts across all regions, while p-tau205 was primarily linked to the frontal cortex, and the non-phosphorylated tau peptides were linked to the temporal cortex. Plasma tau levels decreased as Lewy body pathology progressed, even among individuals at the same tau Braak stage. All plasma biomarkers correlated with creatinine levels, as a marker of renal dysfunction, but this effect was mitigated when using the ratios phospho/non-phospho. DISCUSSION: Understanding how plasma tau biomarkers are influenced by co-pathologies and comorbidities is crucial for their accurate implementation. HIGHLIGHTS: The plasma phosphorylated tau (p-tau)217 ratio, followed by the p-tau205 ratio and p-tau217, were the best-performing biomarkers for detecting neuropathologically confirmed Alzheimer's disease (AD). In high AD cases, p-tau217 showed associations with neurofibrillary tangle (NFT) counts across all regions, while p-tau205 was primarily linked to the frontal cortex, and non-phosphorylated tau peptides were linked to the temporal cortex. We observed a decline in plasma tau levels as Lewy body pathology progressed, even among individuals at the same tau Braak stage. All plasma biomarkers correlated with creatinine levels, as a marker of renal dysfunction, but this effect was mitigated when using the ratios. Plasma p-tau199 displayed a distinct behavior compared to other p-tau species, showing no association with NFT counts in any brain region, but demonstrating significant correlations with brain volume and an effect on survival time.

Indexed as

Alzheimer DiseaseLewy BodiesLewy Body DiseaseNeurofibrillary Tanglestau ProteinsAgedAged, 80 and overBiomarkersBrainCohort StudiesFemaleHumansMalePhosphorylationBiomarkersMAPT protein, humantau Proteinsbloodmass spectrometryneuropathological examinationtau phosphorylation

Identifiers

PMID40791093
PMCPMC12340429

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.