Evidence map›Paper›PMID 39692283›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Association between the Amplification Parameters of the α-Synuclein Seed Amplification Assay and Clinical and Genetic Subtypes of Parkinson's Disease.

Piergiorgio Grillo, Luis Concha-Marambio, Antonio Pisani, Giulietta Maria Riboldi, Un Jung Kang

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 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

5 authors.

Piergiorgio GrilloThe Marlene and Paolo Fresco Institute for Parkinson's and Movement Disorders, Department of Neurology, NYU Langone Health, New York City, New York, USA.ORCID 0000-0001-8196-3914
Luis Concha-MarambioAmprion, R&D Unit, San Diego, California, USA.ORCID 0000-0002-9454-8389
Antonio PisaniDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.ORCID 0000-0002-8432-594X
Giulietta Maria RiboldiThe Marlene and Paolo Fresco Institute for Parkinson's and Movement Disorders, Department of Neurology, NYU Langone Health, New York City, New York, USA.ORCID 0000-0003-0322-5718
Un Jung KangThe Marlene and Paolo Fresco Institute for Parkinson's and Movement Disorders, Department of Neurology, NYU Langone Health, New York City, New York, USA.ORCID 0000-0002-5970-6839

Funding

Study in Parkinson Disease of Exercise Phase 3 Clinical Trial: SPARX3U01NS113851 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniel M. Corcos · 2019 to 2026
$29.6M
Clinical Trial Readiness for Multiple System Atrophy - Resubmission - 1U01NS122419 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HORACIO KAUFMANN · 2022 to 2026
$4.8M
The Role of Myeloid Cells in Parkinson's DiseaseR01NS116006 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Towfique Raj · 2021 to 2026
$4.0M
Early Onset Parkinson’s disease subtypes and pathogenic mechanismsR01NS133742 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Giulietta Maria Riboldi · 2023 to 2026
$2.7M
Biomarkers for parkinsonian disorders in CNS-originating extracellular vesiclesRF1NS126406 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BITAN, GAL · 2023 to 2024
$2.6M
Single Cell Transcriptomic Profiling of Multiple System Atrophy BrainR01NS131658 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Un Jung Kang · 2024 to 2026
$2.0M
Single Cell Transcriptomic Profiling of Multiple System Atrophy BrainR56NS131658 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KANG, UN JUNG · 2023 to 2023
$593k
Michael J Fox Foundation, Parkinson's Foundation, Department of Defense PD210038Ministry of University and Research (MUR)National Recovery and Resilience Plan (NRRP) MNESYS (PE0000006)NEXTGENERATIONEU (NGEU)NIH HHS R01 NS116006NIH HHS R01 NS131658NIH HHS R01 NS133742NIH HHS RF1 NS126406NIH HHS U01 NS113851NIH HHS U01 NS122419NINDS NIH HHS R01 NS116006NINDS NIH HHS R01 NS131658NINDS NIH HHS R01 NS133742NINDS NIH HHS R56 NS131658NINDS NIH HHS RF1 NS126406NINDS NIH HHS U01 NS113851NINDS NIH HHS U01 NS122419The Marlene and Paolo Fresco Institute Post-doctoral Clinical Fellowship
6 · The paper itself

Abstract

backgroundα-Synuclein seed amplification assay on cerebrospinal fluid (CSF-αSyn-SAA) has shown high accuracy for Parkinson's disease (PD) diagnosis. The analysis of CSF-αSyn-SAA parameters may provide useful insight to dissect the heterogeneity of synucleinopathies.

objectiveTo assess differences in CSF-αSyn-SAA amplification parameters in participants with PD stratified by rapid eye movement (REM) sleep behavior disorder (RBD), dysautonomia, GBA, and LRRK2 variants.

methodsClinical and CSF-αSyn-SAA data from the Parkinson's Progression Marker Initiative dataset were used. CSF-αSyn-SAA parameters included maximum fluorescence (F

resultsCSF-αSyn-SAA was positive in 77% of LRRK2-PD, 92.3% of GBA-PD, and 93.8% of sporadic PD. The LRRK2-PD cohort showed longer T50 and TTT, and smaller AUC than GBA-PD (P = 0.029, P = 0.029, P = 0.016, respectively) and sporadic PD (P = 0.034, P = 0.033, P = 0.014, respectively). In the sporadic cohort, CSF-αSyn-SAA parameters were similar between PD with (n = 157) and without (n = 190) RBD, whereas participants with DysA (n = 193) presented shorter T50 (P = 0.026) and larger AUC (P = 0.029) than those without (n = 150).

conclusionCSF-αSyn-SAA parameters vary across genetic and non-genetic PD subtypes at the group level. These differences are mostly driven by the presence of LRRK2 variants and DysA. Significant overlaps in the amplification parameter values exist between groups and limit their use at the individual level. Further studies are necessary to understand the mechanisms of CSF-αSyn-SAA parameter differences. © 2024 International Parkinson and Movement Disorder Society.

Indexed as

alpha-SynucleinParkinson DiseaseAgedBiomarkersFemaleGlucosylceramidaseHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MaleMiddle AgedPrimary DysautonomiasREM Sleep Behavior Disorderalpha-SynucleinBiomarkersGBA protein, humanGlucosylceramidaseLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanSNCA protein, humanGBA1LRRK2Parkinson's diseaseRBDα‐synuclein seed amplification assay

Identifiers

PMID39692283
PMCPMC11904876

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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.