Quantification of cerebrospinal fluid α-synuclein seeds by endpoint dilution seed amplification assay in Parkinson’s disease

Quantitative pathology-specific biomarkers are needed for patients with Parkinson's disease (PD). We estimated the α-syn seeding dose giving 50% of positive seed amplification assay (SAA) reactions (SD50) in serially diluted samples from 260 PD participants, of whom 54 had longitudinal samples. We then evaluated the associations between SD50 values and demographic and clinical parameters, including motor and cognitive scales, REM sleep behaviour disorder (RBD), and hyposmia. Higher SD50 values were significantly associated with older age, longer disease duration, worse motor and cognitive scores, and presence of RBD and visual hallucinations. Baseline SD50 values predicted the development of motor wearing-off and severe cognitive impairment. In participants with longitudinal samples, SD50 values remained substantially stable over time. Quantification of α-syn through endpoint dilution SAA may serve as a potential surrogate marker of LB pathological burden, which may support prognostication and patient stratification.

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Publication Details

Journal
npj Parkinson s Disease
Published
2025-12-01
DOI
https://doi.org/10.1038/s41531-025-01221-7
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
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article

Quantification of cerebrospinal fluid α-synuclein seeds by endpoint dilution seed amplification assay in Parkinson’s disease

Kathrin Brockmann, Simone Baiardi, Stefanie Lerche, Angela Mammana et al.
npj Parkinson s Disease
Parkinson's Disease Mechanisms and Treatments
article

Quantification of cerebrospinal fluid α-synuclein seeds by endpoint dilution seed amplification assay in Parkinson’s disease

Kathrin Brockmann, Simone Baiardi, Stefanie Lerche, Angela Mammana, Piero Parchi, Thomas Gasser, Claudia Schulte, Benjamin Röeben, Ann‐Kathrin Hauser, Christian Deuschle, Isabel Wurster, Andrea Mastrangelo, Alice Ticca, Erica Vittoriosi
article en

Abstract

Quantitative pathology-specific biomarkers are needed for patients with Parkinson's disease (PD). We estimated the α-syn seeding dose giving 50% of positive seed amplification assay (SAA) reactions (SD50) in serially diluted samples from 260 PD participants, of whom 54 had longitudinal samples. We then evaluated the associations between SD50 values and demographic and clinical parameters, including motor and cognitive scales, REM sleep behaviour disorder (RBD), and hyposmia. Higher SD50 values were significantly associated with older age, longer disease duration, worse motor and cognitive scores, and presence of RBD and visual hallucinations. Baseline SD50 values predicted the development of motor wearing-off and severe cognitive impairment. In participants with longitudinal samples, SD50 values remained substantially stable over time. Quantification of α-syn through endpoint dilution SAA may serve as a potential surrogate marker of LB pathological burden, which may support prognostication and patient stratification.

npj Parkinson s DiseaseVol. 12(1)
German Center for Neurodegenerative Diseases (DE), Centre for Movement Disorders (CA), Istituto delle Scienze Neurologiche di Bologna (IT), Hertie Institute for Clinical Brain Research (DE), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Tübingen (DE), University of Bologna (IT)
Bundesministerium für Bildung und Forschung, Ministero della Salute, Deutsches Zentrum für Neurodegenerative Erkrankungen
Openalex Percentile: Top 49%
Parkinson's Disease Mechanisms and Treatments
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