Evidence map›Paper›PMID 41720889›Full record

ArticleScientific reports2026

Identification of altered salivary microRNAs in Cavalier King Charles Spaniels affected by mitral valve disease at different ACVIM stages.

Sara Ghilardi, Gaspare Salvi, Mara Bagardi, Ombretta Balbi, Asia Balgera, Yasmine Dadi, Giovanni Romito, Michele Polli, Maddalena Arigoni, Raffaele Calogero and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Sara GhilardiDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Gaspare SalviDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Mara BagardiDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Ombretta BalbiDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Asia BalgeraDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Yasmine DadiDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Giovanni RomitoDepartment of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
Michele PolliDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Maddalena ArigoniDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Raffaele CalogeroDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Paola G BrambillaDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy.
Cristina LecchiDepartment of Veterinary Medicine and Animal Science, University of Milan, Lodi, Italy. cristina.lecchi@unimi.it.

Funding

Seed4Innovation Scouting Program 2023 of the Università degli Studi di Milano MOOVET - Molecular Diagnostic Tools in Veterinary MedicineUniversity of Milan Piano di Sostegno alla Ricerca (PSR 2023) Linea 2 - Dotazione annuale per attività istituzionali
6 · The paper itself

Abstract

Myxomatous mitral valve disease (MMVD) in Cavalier King Charles Spaniels (CKCSs) can be diagnosed at a young age. Early and sensitive biomarkers related to the disease are currently lacking. MicroRNAs (miRNAs) are involved in the onset and progression of canine MMVD. This study aimed to profile the salivary miRNAs associated with MMVD severity in CKCSs and to identify their target genes. This was a pilot prospective, cross-sectional study. Saliva was collected from twenty-five CKCSs belonging to the American College of Veterinary Internal Medicine (ACVIM) stages A (n. 6), B1 (n. 13), and B2 (n. 6), and salivary miRNAs’ expression was profiled by Next Generation Sequencing. miRNAs’ target genes were identified using bioinformatic tools. Results showed that 25 miRNAs were differentially expressed (DE) between ACVIM A and B1 dogs; 35 DE-miRNAs were modulated in ACVIM B2 compared to B1 CKCSs; 4 miRNAs were up-regulated in ACVIM stage B1 patients compared to both ACVIM stages A and B2. These findings confirm that salivary miRNAs can be successfully quantified in CKCSs and that their expression differs across MMVD severity groups. The DE-miRNAs were associated with signalling pathways related to cellular metabolism, survival, and early inflammatory remodeling. Given the exploratory and cross-sectional design, these miRNAs should be considered candidate, non-invasive indicators associated with disease severity rather than established biomarkers. Further longitudinal and validation studies are needed to assess their diagnostic potential.

Indexed as

Dog DiseasesHeart Valve DiseasesMicroRNAsMitral ValveSalivaAnimalsBiomarkersCross-Sectional StudiesDogsFemaleGene Expression ProfilingMalePilot ProjectsProspective StudiesBiomarkersMicroRNAsBiomarkersCavalier King Charles SpanielsDogmicroRNAMyxomatous mitral valve diseaseSaliva

Identifiers

PMID41720889
PMCPMC13022349

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.