Evidence map›Paper›PMID 41303301›Full record

ArticleInternational journal of molecular sciences2025

Molecular Network Analysis of Circulating microRNAs Highlights miR-17-5p and miR-29a-3p as Potential Biomarkers of Aortic Valve Calcification.

Antonella Galeone, Arianna Minoia, Michele Braggio, Mattia Cominacini, Maria Grazia Romanelli, Luca Dalle Carbonare, Giuseppe Faggian, Giovanni Battista Luciani, Maria Teresa Valenti

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. The role of microRNAs in calcific aortic valve disease.Frontiers in cardiovascular medicine · 2025
    Review
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.

Antonella GaleoneDepartment of Surgery, Dentistry, Pediatrics and Gynecology, Division of Cardiac Surgery, University of Verona, 37126 Verona, Italy.ORCID 0000-0001-5965-6571
Arianna MinoiaDepartment of Engineering for the Innovation Medicine, University of Verona, 37100 Verona, Italy.ORCID 0000-0003-4610-1168
Michele BraggioDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37100 Verona, Italy.ORCID 0000-0001-7163-6194
Mattia CominaciniDepartment of Engineering for the Innovation Medicine, University of Verona, 37100 Verona, Italy.ORCID 0000-0002-4315-0282
Maria Grazia RomanelliDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37100 Verona, Italy.ORCID 0000-0002-7360-1195
Luca Dalle CarbonareDepartment of Engineering for the Innovation Medicine, University of Verona, 37100 Verona, Italy.ORCID 0000-0003-3263-6671
Giuseppe FaggianDepartment of Surgery, Dentistry, Pediatrics and Gynecology, Division of Cardiac Surgery, University of Verona, 37126 Verona, Italy.ORCID 0000-0001-5371-5761
Giovanni Battista LucianiDepartment of Surgery, Dentistry, Pediatrics and Gynecology, Division of Cardiac Surgery, University of Verona, 37126 Verona, Italy.ORCID 0000-0003-0931-018X
Maria Teresa ValentiDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37100 Verona, Italy.ORCID 0000-0003-1166-8033

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcific aortic valve disease (CAVD) is characterized by progressive valve remodeling and calcification. Moreover, microRNAs (miRNAs) are emerging as key regulators of cardiovascular pathology and potential circulating biomarkers. We performed high-throughput miRNA profiling in calcified aortic valve tissue and matched patient serum samples using an array that included 98 human miRNAs. Expression data were log10-transformed and filtered to identify biologically relevant miRNAs. Shared miRNAs between tissue and serum were further validated by quantitative real-time polymerase chain reaction (qRT-PCR) in patients and healthy controls. Of the 49 actively expressed miRNAs, 18 were shared between valve tissue and serum. Thus, qRT-PCR validation revealed significant downregulation of miR-17-5p and miR-29a-3p in CAVD patient serum compared to controls. These results indicate that disease-associated miRNA alterations in calcified valves are mirrored in circulation. miR-17-5p and miR-29a-3p represent promising circulating biomarkers for CAVD, reflecting underlying pathological remodeling and extracellular matrix dysregulation. Our findings provide a framework for non-invasive monitoring of valve calcification and highlight miRNA-mediated pathways as potential therapeutic targets.

Indexed as

Aortic ValveAortic Valve StenosisCalcinosisCirculating MicroRNAGene Regulatory NetworksMicroRNAsAgedBiomarkersCase-Control StudiesFemaleGene Expression ProfilingHumansMaleMiddle AgedBiomarkersCirculating MicroRNAMicroRNAsMIRN17 microRNA, humanMIRN29a microRNA, humanbiomarkercalcific aortic valve diseasemicro-RNA

Identifiers

PMID41303301
PMCPMC12652765

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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.