Evidence map›Paper›PMID 32860338›Full record

ArticleAnnals of clinical and translational neurology2020

Validation of differentially expressed brain-enriched microRNAs in the plasma of PD patients.

Stylianos Ravanidis, Anastasia Bougea, Nikolaos Papagiannakis, Christos Koros, Athina Maria Simitsi, Ioanna Pachi, Marianthi Breza, Leonidas Stefanis, Epaminondas Doxakis

Open access · goldAbstract readValidation Study
In one paragraph

Article in Annals of clinical and translational neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 3 pooled it
2.6field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 3 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. The Role of miRNAs in Parkinson's Disease: A Systematic Review.International journal of molecular sciences · 2025
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  10. Unlocking Parkinson's disease: the role of microRNAs in regulation, diagnosis, and therapy.Apoptosis : an international journal on programmed cell death · 2025
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  14. Exosomal microRNAs in Parkinson's disease: insights into biomarker potential and disease pathology.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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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 2 institutions in 1 country.

Stylianos RavanidisCenter of Basic Research, Biomedical Research Foundation, Academy of Athens, Athens, 11527, Greece.ORCID 0000-0002-8347-218X
Anastasia BougeaCenter of Basic Research, Biomedical Research Foundation, Academy of Athens, Athens, 11527, Greece.
Nikolaos PapagiannakisCenter of Clinical Research, Biomedical Research Foundation, Academy of Athens, Athens, 11527, Greece.ORCID 0000-0002-8401-8472
Christos KorosFirst Department of Neurology, National and Kapodistrian University of Athens Medical School, Athens, 11528, Greece.
Athina Maria SimitsiFirst Department of Neurology, National and Kapodistrian University of Athens Medical School, Athens, 11528, Greece.
Ioanna PachiFirst Department of Neurology, National and Kapodistrian University of Athens Medical School, Athens, 11528, Greece.ORCID 0000-0001-7488-4425
Marianthi BrezaFirst Department of Neurology, National and Kapodistrian University of Athens Medical School, Athens, 11528, Greece.ORCID 0000-0001-9213-7941
Leonidas StefanisCenter of Clinical Research, Biomedical Research Foundation, Academy of Athens, Athens, 11527, Greece.ORCID 0000-0003-3569-8990
Epaminondas DoxakisCenter of Basic Research, Biomedical Research Foundation, Academy of Athens, Athens, 11527, Greece.ORCID 0000-0003-1305-0739
National and Kapodistrian University of Athens · GRAcademy of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is a pressing need to identify and validate, minimally invasive, molecular biomarkers that will complement current practices and increase the diagnostic accuracy in Parkinson's disease (PD). Brain-enriched miRNAs regulate all aspects of neuron development and function; importantly, they are secreted by neurons in amounts that can be readily detected in the plasma. Τhe aim of the present study was to validate a set of previously identified brain-enriched miRNAs with diagnostic potential for idiopathic PD and recognize the molecular pathways affected by these deregulated miRNAs.

methodsRT-qPCR was performed in the plasma of 92 healthy controls and 108 idiopathic PD subjects. Statistical and in silico analyses were used to validate deregulated miRNAs and pathways in PD, respectively.

resultsmiR-22-3p, miR-124-3p, miR-136-3p, miR-154-5p, and miR-323a-3p levels were found to be differentially expressed between healthy controls and PD patients. miR-330-5p, miR-433-3p, and miR-495-3p levels were overall higher in male subjects. Most of these miRNAs are clustered at Chr14q32 displaying CREB1, CEBPB, and MAZ transcription factor binding sites. Gene Ontology annotation analysis of deregulated miRNA targets revealed that "Protein modification," "Transcription factor activity," and "Cell death" terms were over-represented. Kyoto Encyclopedia of Genes and Genome analysis revealed that "Long-term depression," "TGF-beta signaling," and "FoxO signaling" pathways were significantly affected.

interpretationWe validated a panel of brain-enriched miRNAs that can be used along with other measures for the detection of PD, revealed molecular pathways targeted by these deregulated miRNAs, and identified upstream transcription factors that may be directly implicated in PD pathogenesis.

Indexed as

AgedBiomarkersFemaleHumansMaleMicroRNAsMiddle AgedParkinson DiseaseBiomarkersMicroRNAs

Identifiers

PMID32860338
PMCPMC7480914
OpenAlexW3082660258

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.