Evidence map›Paper›PMID 39822296›Full record

ArticleAlzheimer's & dementia (Amsterdam, Netherlands)

Toward alpha-synuclein seed amplification assay in clinical practice.

Mathieu Verdurand, Flora Kaczorowski, Sophie Dautricourt, Virginie Desestret, Maïté Formaglio, Hélène Mollion, Gil Petitnicolas, Ali Afifi, Anthony Fourier, Antoine Garnier-Crussard and 1 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia (Amsterdam, Netherlands). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Intrinsic capacity in Lewy body dementia: a review.The Journal of frailty & aging · 2025
    Review
  10. Implications and opportunities regarding biological frameworks in overt and prodromal dementia with Lewy bodies.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Review
  11. Review
  12. Late-onset dementia with leukoencephalopathy and aCerebral circulation - cognition and behavior · 2025
    Article
  13. Cerebrospinal fluidAlzheimer's & dementia (New York, N. Y.)
    Article
  14. Toward alpha-synuclein seed amplification assay in clinical practice.Alzheimer's & dementia (Amsterdam, Netherlands)
    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

11 authors.

Mathieu VerdurandBiochemistry and Molecular Biology Department Neurodegenerative Pathologies LBMMS Hospices Civils de Lyon Lyon France.ORCID https://orcid.org/0000-0003-2619-3907
Flora KaczorowskiBiochemistry and Molecular Biology Department Neurodegenerative Pathologies LBMMS Hospices Civils de Lyon Lyon France.
Sophie DautricourtLyon Memory Resources and Research Center Hospices Civils de Lyon Lyon France.
Virginie DesestretLyon Memory Resources and Research Center Hospices Civils de Lyon Lyon France.
Maïté FormaglioLyon Memory Resources and Research Center Hospices Civils de Lyon Lyon France.
Hélène MollionLyon Memory Resources and Research Center Hospices Civils de Lyon Lyon France.
Gil PetitnicolasToulon Memory Clinic Hôpital Sainte Musse Toulon-La Seyne Sur Mer France.
Ali AfifiMâcon Memory Clinic Hôpital de Mâcon Mâcon France.
Anthony FourierBiochemistry and Molecular Biology Department Neurodegenerative Pathologies LBMMS Hospices Civils de Lyon Lyon France.
Antoine Garnier-CrussardLyon Memory Resources and Research Center Hospices Civils de Lyon Lyon France.
Isabelle QuadrioBiochemistry and Molecular Biology Department Neurodegenerative Pathologies LBMMS Hospices Civils de Lyon Lyon France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSeed amplification assays (SAAs) demonstrate remarkable diagnostic performance in alpha-synucleinopathies. However, existing protocols lack accessibility in routine laboratories, mainly due to the requirement for in-house production of recombinant alpha-synuclein (aSyn). This study proposes a cerebrospinal fluid (CSF) aSyn-SAA protocol using solely commercial reagents to facilitate its clinical implementation.

methodsRoutine clinical care CSF samples from 126 patients, comprising 47 with Lewy body diseases (LBD) (41 with dementia with Lewy bodies, six with Parkinson's disease), 37 without alpha-synucleinopathy, and 42 with Alzheimer's disease (AD), underwent assessment for aSyn-SAA activity.

resultsCSF aSyn-SAA showed a sensitivity of 72.3% and a specificity of 100% when distinguishing clinically diagnosed LBD patients from those without alpha-synucleinopathy. In AD patients, 14.3% were tested positive for aSyn. DISCUSSION: The commercial-only CSF aSyn-SAA protocol exhibited excellent specificity when applied to a real-life cohort, signaling progress toward the accessibility of an aSyn biomarker in clinical settings. Highlights: Diagnosis of LBD through aSyn-SAA lacks accessibility.This commercial-only aSyn-SAA has satisfactory performance in a real-life cohort.A negative aSyn-SAA does not completely exclude a synucleinopathy.Some technical points must be considered when developing aSyn-SAA.aSyn-SAA must be confined to expert laboratories due to prion-like risk management.

Indexed as

alpha‐synuclein (α‐synuclein)aSynbiomarkerbrain homogenate (BH)cerebrospinal fluid (CSF)dementia with Lewy bodies (DLB)Lewy body disease (LBD)neurodegenerative diseasesParkinson's disease (PD)proteinopathiesreal‐life cohortreal‐time quaking‐induced conversion (RT‐QuIC)seed amplification assay (SAA)synucleinopathies

Identifiers

PMID39822296
PMCPMC11736632

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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.