Evidence map›Paper›PMID 40568761›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Evaluation of Induced Pluripotent Stem Cell-Derived Dopaminergic Neurons from Siblings with Gaucher Disease Discordant for Parkinsonism.

Ellen Hertz, Krystyna Rytel, Gani Perez, Ying Hao, Ziyi Li, Charis Ma, Kate Andersh, Yue Andy Qi, Emory Ryan, Grisel Lopez and 3 more

Erratum issuedAbstract 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. An erratum has been issued. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Ellen HertzMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Krystyna RytelMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Gani PerezMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Ying HaoCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Ziyi LiCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Charis MaMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Kate AndershCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-7709-4111
Yue Andy QiCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Emory RyanMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Grisel LopezMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Nahid TayebiMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Ellen SidranskyMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-3019-8500
Yu ChenMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-5438-7309

Funding

Aligning Science Across Parkinson's ASAP-000458NHGRI NIH HHSNIA NIH HHS ZO1 AG000534NINDS NIH HHS
6 · The paper itself

Abstract

backgroundIn Gaucher disease (GD), glucocerebrosidase (GCase) deficiency results from biallelic pathogenic GBA1 variants. While GBA1 variants are a major risk factor for Parkinson's disease (PD), most patients with GD never develop parkinsonism.

objectivesTo understand factors impacting PD penetrance in patients with GD by comparing induced pluripotent stem cell (iPSC)-derived dopaminergic neurons (DANs) from GD siblings discordant for PD.

methodsiPSCs, reprogrammed from two different sibling pairs where both siblings had GD but only one developed PD, were differentiated into DANs. In one family, DAN enrichment was achieved via geneticin selection and proteomic evaluations were performed.

resultsGCase and lipid substrate levels were similar in GD and GD/PD DANs. After geneticin selection, proteomic analysis of the enriched DANs showed upregulation of molecular chaperones in the GD/PD line.

conclusionPD discordance in both sets of GD siblings did not correlate with GCase or lipid substrate levels in DANs, implicating the involvement of other modifiers. Published 2025. This article is a U.S. Government work and is in the public domain in the USA. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Dopaminergic NeuronsGaucher DiseaseInduced Pluripotent Stem CellsParkinson DiseaseParkinsonian DisordersAdultFemaleGlucosylceramidaseHumansMaleMiddle AgedSiblingsGlucosylceramidasedopaminergic neuron differentiationGaucher diseaseGBA1neurodegenerationParkinson's disease

Identifiers

PMID40568761
PMCPMC12371625

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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.