Evidence map›Paper›PMID 41814005›Full record

ArticleNature medicine2026

Blood phosphorylated tau elevation as a biomarker in immunoglobulin light chain and transthyretin amyloidosis.

Stephan A Kaeser, Stephanie A Schultz, Anna Hofmann, Lisa M Häsler, Ying Xu, Marius Lambert, Ulrike Obermüller, Kathrin Brockmann, Johan Bijzet, Hans Nienhuis and 6 more

Abstract read
In one paragraph

Article in Nature medicine, 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. Alzheimer's & dementia (Amsterdam, Netherlands)
    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

16 authors.

Stephan A Kaeser *German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0000-0002-4188-5111
Stephanie A Schultz *Department of Neurology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8460-4415
Anna Hofmann *German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Lisa M HäslerGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Ying XuGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0009-0002-3728-6519
Marius LambertGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Ulrike ObermüllerGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Kathrin BrockmannGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0000-0002-7515-8596
Johan BijzetDepartment of Laboratory Medicine, Groningen Amyloidosis Center of Expertise Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID http://orcid.org/0000-0002-0375-4460
Hans NienhuisDepartment of Internal Medicine, Groningen Amyloidosis Center of Expertise, University Medical Centre Groningen, Groningen, the Netherlands. h.l.a.nienhuis@umcg.nl.ORCID http://orcid.org/0000-0003-3974-6830
Mario NuvoloneDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.ORCID http://orcid.org/0000-0001-8334-1684
Laura ObiciAmyloidosis Research and Treatment Center, IRCCS Fondazione Policlinico San Matteo, Pavia, Italy.
Giovanni PalladiniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy. giovanni.palladini@unipv.it.ORCID http://orcid.org/0000-0001-5994-5138
Ute HegenbartAmyloidosis Center, Medical Department V, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-1917-6746
Stefan O SchönlandAmyloidosis Center, Medical Department V, University Hospital Heidelberg, Heidelberg, Germany. stefan.schoenland@med.uni-heidelberg.de.ORCID http://orcid.org/0000-0002-4853-5579
Mathias JuckerGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany. mathias.jucker@uni-tuebingen.de.ORCID http://orcid.org/0000-0001-9045-1072

Funding

Identifying variations in gamma-secretase function that are critical determinants of clinical and biomarker progression of Autosomal Dominant Alzheimer's disease: From mechanism to clinical trialsK01AG084816 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Stephanie Schultz · 2024 to 2026
$387k
NIA NIH HHS K01 AG084816
6 · The paper itself

Abstract

Elevated blood levels of phosphorylated tau (p-tau) are diagnostic of Alzheimer disease and are associated with the deposition of amyloid-β in the cerebral neuropil. Elevated p-tau levels have also been associated with cerebral deposition of Danish amyloid and prion protein amyloid. Here we analyzed p-tau in serum from four different cohorts of people with the most common types of systemic amyloidosis, transthyretin (ATTR) amyloidosis and immunoglobulin light chain (AL) amyloidosis. We found higher levels of serum p-tau181 in the AL and ATTR groups than in controls. Subsequent analyses revealed that these effects were more pronounced in the presence of polyneuropathy (PNP) and in AL compared to ATTR amyloidosis. Individuals with different forms of PNP that were not due to amyloidosis did not exhibit elevated p-tau181 levels. In cases of presymptomatic (genetic) ATTR, p-tau181 levels increased as a function of predicted years from symptom onset. Additional measurement of p-tau217 in one cohort revealed similar increases, and discriminated people with AL and those with ATTR from controls equally as well as p-tau181. These findings suggest that elevated serum p-tau levels are not specific to Alzheimer disease and may also serve as a diagnostic tool of ATTR and AL amyloidosis, with potential utility in distinguishing amyloidosis-related PNP from PNP of other etiologies.

Indexed as

Amyloid Neuropathies, FamilialAmyloidosisImmunoglobulin Light Chainstau ProteinsAgedBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedPhosphorylationPolyneuropathiesPrealbuminBiomarkersImmunoglobulin Light ChainsPrealbumintau Proteins

Identifiers

PMID41814005
PMCPMC13190286

What OpenQuestion holds

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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.