Evidence map›Paper›PMID 41048081›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

A Biomarker-Based Classification of Corticobasal Syndrome.

Carla Palleis, Alexander Maximilian Bernhardt, Endy Weidinger, Urban M Fietzek, Alexander Jäck, Sabrina Katzdobler, Johannes Gnörich, Theresa Bauer, Nicolai Franzmeier, Robert Perneczky and 4 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Toward the prevention of clinically manifest Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
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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

14 authors.

Carla Palleis *Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.ORCID https://orcid.org/0000-0002-4331-8145
Alexander Maximilian Bernhardt *Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.ORCID https://orcid.org/0000-0002-2572-5062
Endy WeidingerDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Urban M FietzekDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Alexander JäckDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Sabrina KatzdoblerDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.ORCID https://orcid.org/0000-0002-3512-5984
Johannes GnörichDepartment of Nuclear Medicine, LMU University Hospital, LMU Munich, Munich, Germany.
Theresa BauerDepartment of Nuclear Medicine, LMU University Hospital, LMU Munich, Munich, Germany.
Nicolai FranzmeierMunich Cluster for Systems Neurology (SyNergy), Munich, Germany.
Robert PerneczkyMunich Cluster for Systems Neurology (SyNergy), Munich, Germany.
German Imaging Initiative for Tauopathies (GII4T)
Matthias Brendel *Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.ORCID https://orcid.org/0000-0002-9247-2843
Johannes Levin *Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Günter U Höglinger *Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.

Funding

Alzheimer Forschung Initiative 19063pAlzheimer Forschung Initiative e.V. 19063pDeutsche Forschungsgemeinschaft BR4580/1-1/RO5194/1-1Deutsche Forschungsgemeinschaft EXC 2145 SyNergy: ID 390857198German Center for Neurodegenerative DiseasesGerman Ministry of Research and Education FKZ161L0214BGerman Ministry of Research and Education FKZ161L0214C CLINSPECT-MGerman Parkinson's AssociationMichael J. Fox FoundationMunich Cluster for Systems Neurology 390857198NOMIS FoundationThiemann Stiftung and Else-Kröner-Fresenius-StiftungVolkswagen Stiftung/Lower Saxony Ministry for Science/Petermax-Müller Foundation
6 · The paper itself

Abstract

backgroundCorticobasal syndrome (CBS) is a clinically defined syndrome with progressive movement and cortical dysfunction, caused by various underlying pathologies, most commonly tau-predominant pathologies such as progressive supranuclear palsy and corticobasal degeneration, or Alzheimer's disease (AD). Lewy-type α-synucleinopathies (LTS), TDP-43 proteinopathies, and mixed pathologies may also underlie CBS. The clinical impact of these pathologies remains poorly understood.

objectivesTo subclassify CBS patients in vivo using biomarkers for amyloid-β (Aβ), Tau, and α-synuclein (αSyn), and assess the clinical relevance of this stratification.

methodsWe conducted a prospective cohort study of 50 CBS patients at LMU University Hospital Munich. Biomarker analysis included cerebrospinal fluid (CSF) Aβ42 and Aβ42/40, [

resultsTau positivity was found in 90% of CBS cases, Aβ in 28%, and αSyn in 24%. Stratification identified: 52% consistent with tau-predominant pathology, 18% with AD, 10% with AD+LTS, 10% with tau-predominant+LTS, 4% with isolated LTS, and 6% unclassified. αSyn positivity was more frequent in AD-CBS (36%) than in tau-predominant-CBS (16%). Aβ-positive cases showed greater cognitive impairment; Tau positivity correlated with worse motor symptoms; αSyn-positive patients had milder motor symptoms, slower progression, and lower NfL levels.

conclusionsCBS is molecularly heterogeneous. Biomarker-based classification may enhance diagnostic precision and support personalized therapeutic strategies. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Corticobasal DegenerationAgedAged, 80 and overalpha-SynucleinAmyloid beta-PeptidesBiomarkersFemaleHumansMaleMiddle AgedPeptide FragmentsPositron-Emission TomographyProspective Studiestau Proteinsalpha-SynucleinAmyloid beta-Peptidesamyloid beta-protein (1-42)BiomarkersPeptide Fragmentstau Proteinsproteinopathiestau‐PETα‐synuclein seed amplification assayβ‐amyloid

Identifiers

PMID41048081
PMCPMC12882055

What OpenQuestion 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 OpenQuestion graph.