Evidence map›Paper›PMID 24959119›Full record

ArticleFrontiers in cellular neuroscience2014

Identification of circulating microRNAs for the differential diagnosis of Parkinson's disease and Multiple System Atrophy.

Annamaria Vallelunga, Marco Ragusa, Stefania Di Mauro, Tommaso Iannitti, Manuela Pilleri, Roberta Biundo, Luca Weis, Cinzia Di Pietro, Angela De Iuliis, Alessandra Nicoletti and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 4 pooled it
9.1field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 4 syntheses or guidelines pooled it, 173 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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  16. Fluid biomarkers in atypical Parkinsonism: current state and future perspectives.Journal of neural transmission (Vienna, Austria : 1996) · 2025
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46 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 2 countries.

Annamaria VallelungaMolecular Neurobiology Laboratory, Department for Parkinson's Disease, IRCCS Hospital San Camillo Venice, Italy.
Marco RagusaUnit of Molecular, Genome and Complex Systems BioMedicine, Department Gian Filippo Ingrassia, University of Catania Catania, Italy.
Stefania Di MauroUnit of Molecular, Genome and Complex Systems BioMedicine, Department Gian Filippo Ingrassia, University of Catania Catania, Italy.
Tommaso IannittiSchool of Biomedical Sciences, University of Leeds Leeds, UK.
Manuela PilleriMolecular Neurobiology Laboratory, Department for Parkinson's Disease, IRCCS Hospital San Camillo Venice, Italy.
Roberta BiundoMolecular Neurobiology Laboratory, Department for Parkinson's Disease, IRCCS Hospital San Camillo Venice, Italy.
Luca WeisMolecular Neurobiology Laboratory, Department for Parkinson's Disease, IRCCS Hospital San Camillo Venice, Italy.
Cinzia Di PietroUnit of Molecular, Genome and Complex Systems BioMedicine, Department Gian Filippo Ingrassia, University of Catania Catania, Italy.
Angela De IuliisDepartment of Medicine, University of Padua Padua, Italy.
Alessandra NicolettiSection of Neuroscience University of Catania, Department GF Ingrassia, University of Catania Catania, Italy.
Mario ZappiaSection of Neuroscience University of Catania, Department GF Ingrassia, University of Catania Catania, Italy.
Michele PurrelloUnit of Molecular, Genome and Complex Systems BioMedicine, Department Gian Filippo Ingrassia, University of Catania Catania, Italy.
Angelo AntoniniMolecular Neurobiology Laboratory, Department for Parkinson's Disease, IRCCS Hospital San Camillo Venice, Italy.
University of Catania · ITIRCCS San Camillo Hospital · ITUniversity of Leeds · GBUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is a progressive neurodegenerative disorder which may be misdiagnosed with atypical conditions such as Multiple System Atrophy (MSA), due to overlapping clinical features. MicroRNAs (miRNAs) are small non-coding RNAs with a key role in post-transcriptional gene regulation. We hypothesized that identification of a distinct set of circulating miRNAs (cmiRNAs) could distinguish patients affected by PD from MSA and healthy individuals. Results. Using TaqMan Low Density Array technology, we analyzed 754 miRNAs and found 9 cmiRNAs differentially expressed in PD and MSA patients compared to healthy controls. We also validated a set of 4 differentially expressed cmiRNAs in PD and MSA patients vs. controls. More specifically, miR-339-5p was downregulated, whereas miR-223(*), miR-324-3p, and mir-24 were upregulated in both diseases. We found cmiRNAs specifically deregulated in PD (downregulation of miR-30c and miR-148b) and in MSA (upregulation of miR-148b). Finally, comparing MSA and PD, we identified 3 upregulated cmiRNAs in MSA serum (miR-24, miR-34b, miR-148b). Conclusions. Our results suggest that cmiRNA signatures discriminate PD from MSA patients and healthy controls and may be considered specific, non-invasive biomarkers for differential diagnosis.

Indexed as

atypical parkinsonian disorderscirculating microRNAsearly diagnosismicroRNAsMultiple System AtrophyParkinson's disease

Identifiers

PMID24959119
PMCPMC4051126
OpenAlexW2118614725

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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.