Evidence map›Paper›PMID 39546628›Full record

ArticleBrain : a journal of neurology2025

Single-nucleus transcriptomics reveals disease- and pathology-specific signatures in α-synucleinopathies.

Gonzalo S Nido, Martina Castelli, Sepideh Mostafavi, Anna Rubiolo, Omnia Shadad, Guido Alves, Ole-Bjørn Tysnes, Irene H Flønes, Christian Dölle, Charalampos Tzoulis

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

10 authors.

Gonzalo S NidoNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Martina CastelliNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Sepideh MostafaviNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Anna RubioloNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Omnia ShadadNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Guido AlvesThe Norwegian Centre for Movement Disorders and Department of Neurology, Stavanger University Hospital, 4068 Stavanger, Norway.
Ole-Bjørn TysnesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Irene H FlønesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Christian DölleNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Charalampos TzoulisNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0003-0341-5191

Funding

Bergen Research Foundation BFS2017REK05Research Council of Norway 288164Western Norway Regional Health Authority F-10229-D11661
6 · The paper itself

Abstract

α-Synucleinopathies are progressive neurodegenerative disorders characterized by intracellular aggregation of α-synuclein, but their molecular pathogenesis remains unknown. Here, we explore cell-specific changes in gene expression across different α-synucleinopathies. We perform single-nucleus RNA sequencing on nearly 300 000 nuclei from the prefrontal cortex of individuals with idiopathic Parkinson's disease (PD, n = 20), Parkinson's disease caused by LRRK2 mutations (LRRK2-PD, n = 7), multiple system atrophy (n = 6) and healthy controls (n = 13). Idiopathic PD and LRRK2-PD exhibit a largely overlapping cell type-specific signature, which is distinct from that of multiple system atrophy and includes an overall decrease of the transcriptional output in neurons. Notably, most of the differential expression signal in idiopathic PD and LRRK2-PD is concentrated in a specific deep cortical neuronal subtype expressing adrenoceptor alpha 2A. Although most differentially expressed genes are highly cell type and disease specific, PDE10A is found to be downregulated consistently in most cortical neurons and across all three diseases. Finally, exploiting the variable presence and/or severity of α-synuclein pathology in LRRK2-PD and idiopathic PD, we identify cell type-specific signatures associated with α-synuclein pathology, including a neuronal upregulation of SNCA itself, encoding α-synuclein. Our findings provide new insights into the cell-specific transcriptional landscape of the α-synucleinopathy spectrum.

Indexed as

Parkinson DiseaseSynucleinopathiesTranscriptomeAgedalpha-SynucleinFemaleGene Expression ProfilingHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MaleMiddle AgedMultiple System AtrophyMutationNeuronsPrefrontal Cortexalpha-SynucleinLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanLewy pathologyLRRK2multiple system atrophynuclear transcriptomicsParkinson’s diseasesingle cell

Identifiers

PMID39546628
PMCPMC12073976

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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.