Evidence map›Paper›PMID 38331996›Full record

ArticleNPJ Parkinson's disease2024

Large-scale proteomics analysis of five brain regions from Parkinson's disease patients with a GBA1 mutation.

Shani Blumenreich, Tamar Nehushtan, Meital Kupervaser, Tali Shalit, Alexandra Gabashvili, Tammar Joseph, Ivan Milenkovic, John Hardy, Anthony H Futerman

Open access · goldAbstract read
In one paragraph

Article in NPJ Parkinson's disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  9. Proteomic insights into the biology of dopaminergic neurons.Frontiers in molecular neuroscience · 2025
    Review
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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

9 authors at 3 institutions in 3 countries.

Shani BlumenreichDepartment of Biomolecular Sciences, Rehovot, 76100, Israel.
Tamar NehushtanDepartment of Biomolecular Sciences, Rehovot, 76100, Israel.
Meital KupervaserNancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, 76100, Israel.
Tali ShalitNancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, 76100, Israel.ORCID http://orcid.org/0009-0005-2651-1591
Alexandra GabashviliNancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, 76100, Israel.
Tammar JosephDepartment of Biomolecular Sciences, Rehovot, 76100, Israel.
Ivan MilenkovicDepartment of Biomolecular Sciences, Rehovot, 76100, Israel.ORCID http://orcid.org/0000-0002-2990-0243
John HardyDepartment of Neurogenerative Disease, UCL Dementia Research Institute, University College London, London, WC1N 3BG, UK.
Anthony H FutermanDepartment of Biomolecular Sciences, Rehovot, 76100, Israel. tony.futerman@weizmann.ac.il.ORCID http://orcid.org/0000-0003-0013-0115
Weizmann Institute of Science · ILMedical University of Vienna · ATUK Dementia Research Institute · GB

Funding

Austrian Science Fund FWF J 4493
6 · The paper itself

Abstract

Despite being the second most common neurodegenerative disorder, little is known about Parkinson's disease (PD) pathogenesis. A number of genetic factors predispose towards PD, among them mutations in GBA1, which encodes the lysosomal enzyme acid-β-glucosidase. We now perform non-targeted, mass spectrometry based quantitative proteomics on five brain regions from PD patients with a GBA1 mutation (PD-GBA) and compare to age- and sex-matched idiopathic PD patients (IPD) and controls. Two proteins were differentially-expressed in all five brain regions whereas significant differences were detected between the brain regions, with changes consistent with loss of dopaminergic signaling in the substantia nigra, and activation of a number of pathways in the cingulate gyrus, including ceramide synthesis. Mitochondrial oxidative phosphorylation was inactivated in PD samples in most brain regions and to a larger extent in PD-GBA. This study provides a comprehensive large-scale proteomics dataset for the study of PD-GBA.

Identifiers

PMID38331996
PMCPMC10853186
OpenAlexW4391648198

What OpenQuestion holds

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LicenceCC BY
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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.