Evidence map›Paper›PMID 39689039›Full record

ArticleBrain : a journal of neurology2025

Alpha-synuclein seed amplification assay longitudinal outcomes in Lewy body disease spectrum.

Andrea Mastrangelo, Angela Mammana, Sara Hall, Erik Stomrud, Corrado Zenesini, Marcello Rossi, Shorena Janelidze, Alice Ticca, Sebastian Palmqvist, Franco Magliocchetti and 4 more

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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.

Andrea MastrangeloDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
Angela MammanaIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Sara HallClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.ORCID 0000-0001-6585-9105
Erik StomrudClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.
Corrado ZenesiniIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Marcello RossiIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Shorena JanelidzeClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.
Alice TiccaDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
Sebastian PalmqvistClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.ORCID 0000-0002-9267-1930
Franco MagliocchettiIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Simone BaiardiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
Niklas Mattsson-CarlgrenClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.ORCID 0000-0002-8885-7724
Oskar HanssonClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund 22002, Sweden.ORCID 0000-0001-8467-7286
Piero ParchiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.ORCID 0000-0002-9444-9524

Funding

Alzheimer's Association SG-23-1061717Alzheimer's Association ZEN24-1069572Cure Alzheimer's fundEuropean Research Council ADG-101096455GHR FoundationKnut and Alice Wallenberg Foundation 2022-0231Ministero della SaluteMinistry of University and ResearchNational Recovery and Resilience Plan PE0000006#NextGenerationEUParkinson foundation of Sweden 1412/22Regionalt Forskningsstöd 2022-1259Regionalt Forskningsstöd 2022-Projekt0080Regionalt Forskningsstöd 2022-Projekt0107Ricerca CorrenteRönström Family Foundation WASP/DDLS22-066Skåne University Hospital Foundation 2020-O000028Strategic Research Area MultiParkSwedish Alzheimer Foundation AF-980907Swedish Alzheimer Foundation AF-994229Swedish Brain Foundation FO2021-0293Swedish Brain Foundation FO2023-0163Swedish Research Council 2021-02219Swedish Research Council 2022-00775
6 · The paper itself

Abstract

Evidence from neuropathological cohorts indicates that a CSF α-synuclein (α-syn) seed amplification assay (SAA) might provide quantitative kinetic parameters correlating with α-syn pathology burden in patients with Lewy body disease (LBD). Studies are needed to assess their longitudinal trend during the presymptomatic and clinical disease phases and their correlation with measures of disease progression. We aimed to assess the baseline α-syn CSF SAA kinetic parameters, their longitudinal variations and associations with clinical outcomes in a longitudinal cohort of repeatedly sampled LBD patients, including clinically unimpaired (asymptomatic LBD) and neurologically impaired individuals. Participants from the prospective BioFINDER-1 study with longitudinal CSF collections (n = 718) were screened by α-syn SAA. CSF samples were tested in four replicates blinded to clinical diagnoses. The number of positive replicates (Nrep), the time needed by the fluorescence signal to reach the threshold (Lag) and the highest intensity of the fluorescent signal were analysed at baseline (time of first positive SAA) in all participants and longitudinally in those with at least two α-syn-positive CSF samples available. One hundred and ninety-six individuals (whole cohort) showing α-syn seeding activity were included. Of those, 170 participants tested positive by SAA in all available samples, while 26 converted from a negative to a positive test result during follow-up (LBD-converters), suggesting an early LBD stage. At baseline, LBD-converters showed lower Nrep (P = 0.001) and a longer Lag (P = 0.001) than subjects displaying α-syn seeding activity from the first available sample. The Nrep increased longitudinally in the whole cohort [β = 0.09, 95% confidence interval (95% CI) 0.06-0.12, P < 0.001], in asymptomatic LBD (β = 0.15, 95% CI 0.09-0.21, P < 0.001) and in Parkinson's disease individuals without dementia (β = 0.07, 95% CI 0.02-0.12, P = 0.01). The Lag decreased longitudinally in asymptomatic LBD (β = -0.24, 95% CI -0.42 to -0.06, P = 0.008). Baseline Nrep predicted the subsequent appearance of dementia in the whole cohort [hazard ratio (HR) 1.57, 95% CI 1.19-2.07, P = 0.001] and the Parkinson's disease subgroup (HR 1.83, 95% CI 1.17-2.85, P = 0.008). The difference between the Lag at each sampling and that at baseline was negatively associated with the appearance of dementia in the whole cohort (HR 0.76, 95% CI 0.59-0.99, P = 0.04) and in the Parkinson's disease subgroup (HR 0.69, 95% CI 0.50-0.95, P = 0.02). The α-syn SAA parameters Nrep and Lag showed associations with the LBD stage and the development of dementia. Furthermore, their longitudinal variation is coherent with progression of pathology over time. These data support the use of SAA kinetic parameters to monitor disease progression and therapeutic response.

Indexed as

alpha-SynucleinLewy Body DiseaseAgedAged, 80 and overBiomarkersDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective Studiesalpha-SynucleinBiomarkersdisease progressionkinetic parametersLewy body diseaselongitudinal studyprionseed amplification assay

Identifiers

PMID39689039
PMCPMC12129724

What OpenQuestion holds

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LicenceCC BY-NC
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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.