Evidence map›Paper›PMID 39957200›Full record

ArticleJournal of Parkinson's disease2024

CSF GPNMB in Parkinson's disease: A potential association with age and microglial activation.

Xi-Chen Zhu, Yasuaki Mizutani, Reiko Ohdake, Harutsugu Tatebe, Toshiki Maeda, Sayuri Shima, Akihiro Ueda, Mizuki Ito, Shinji Ito, Takahiko Tokuda and 1 more

Abstract read
In one paragraph

Article in Journal of Parkinson's disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

11 authors.

Xi-Chen ZhuDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0001-8468-876X
Yasuaki MizutaniDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0002-5709-8526
Reiko OhdakeDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Harutsugu TatebeDepartment of Functional Brain Imaging, Institute for Quantum Medical Science, National Institutes for Quantum Science and Technology, Chiba, Chiba, Japan.
Toshiki MaedaDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Sayuri ShimaDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0003-1761-0123
Akihiro UedaDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0002-9636-3011
Mizuki ItoDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Shinji ItoDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Takahiko TokudaDepartment of Functional Brain Imaging, Institute for Quantum Medical Science, National Institutes for Quantum Science and Technology, Chiba, Chiba, Japan.
Hirohisa WatanabeDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent evidence suggests a link between glycoprotein non-metastatic melanoma protein B (GPNMB) and Parkinson's disease (PD) pathogenesis. Although elevated plasma GPNMB levels associated with disease severity have been reported in PD, cerebrospinal fluid (CSF) alterations remain elusive.

objectiveTo explore CSF GPNMB alterations and its clinical significance in PD.

methodsThis study enrolled 118 sporadic PD patients and 40 controls. We examined the potential associations between CSF GPNMB levels and the clinical characteristics or biomarkers of neurodegenerative pathogenesis.

resultsPD patients had higher CSF GPNMB levels than controls (

conclusionsElevated CSF GPNMB levels, linked with age and microglial activation, may be a valuable marker for understanding the interplay between aging, neuroinflammation, and PD pathology.

Indexed as

Cognitive DysfunctionMembrane GlycoproteinsMicrogliaParkinson DiseaseAgedAge FactorsBiomarkersFemaleGPI-Linked ProteinsHumansMaleMiddle AgedSeverity of Illness IndexBiomarkersGPI-Linked ProteinsGPNMB protein, humanMembrane Glycoproteinsagecerebrospinal fluidglycoprotein non-metastatic melanoma protein Bparkinson's diseasesoluble triggering receptor expressed on myeloid cells 2

Identifiers

PMID39957200
PMCPMC13348315

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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.