Evidence map›Paper›PMID 39553198›Full record

ArticleFrontiers in veterinary science2024

Assessing the use of blood microRNA expression patterns for predictive diagnosis of myxomatous mitral valve disease in dogs.

Javier Palarea-Albaladejo, Elizabeth F Bode, Catheryn Partington, Mattia Basili, Elzbieta Mederska, Hannah Hodgkiss-Geere, Paul Capewell, Caroline Chauché, Robert M Coultous, Eve Hanks and 1 more

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Recent advances in omics-based research of mitral valve disease.Frontiers in cardiovascular medicine · 2026
    Review
  5. Review
  6. Article
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.

Javier Palarea-AlbaladejoDepartment of Computer Science, Applied Mathematics and Statistics, University of Girona, Girona, Spain.
Elizabeth F BodeDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Catheryn PartingtonDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Mattia BasiliDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Elzbieta MederskaDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Hannah Hodgkiss-GeereDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Paul CapewellSchool of Molecular Biosciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Caroline ChauchéCentre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Robert M CoultousMI:RNA Ltd, Edinburgh, United Kingdom.
Eve HanksMI:RNA Ltd, Edinburgh, United Kingdom.
Joanna Dukes-McEwanDepartment of Small Animal Clinical Science, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myxomatous mitral valve disease (MMVD) is a common, acquired, and progressive canine heart disease. The presence of heart murmur and current cardiac biomarkers are useful in MMVD cases but are not sufficiently discriminatory for staging an individual patient. Objectives: This study aimed to conduct a preliminary assessment of canine serum and plasma expression profiles of 15 selected miRNA markers for accurate discrimination between MMVD patients and healthy controls. Additionally, we aim to evaluate the effectiveness of this method in differentiating between pre-clinical (stage B1/B2) and clinical (stage C/D) MMVD patients. Animals: Client-owned dogs ( Methods: A multicenter, cross-sectional, prospective investigation was conducted. MicroRNA expression profiles were compared among dogs, and these profiles were used as input for predictive modeling. This approach aimed to distinguish between healthy controls and MMVD patients, as well as to achieve a more fine-grained differentiation between pre-clinical and clinical MMVD patients. Results: Performance metrics revealed a compelling ability of the method to differentiate healthy controls from dogs with MMVD (sensitivity 0.85; specificity 0.82; and accuracy 0.83). For the discrimination between the pre-clinical ( Conclusion and clinical importance: The use of miRNA expression profiles in combination with customized probabilistic predictive modeling shows good scope to devise a reliable diagnostic tool to distinguish healthy controls from MMVD cases (stages B1 to D). Investigation into the ability to discriminate between the pre-clinical and clinical MMVD cases using the same method yielded promising early results, which could be further enhanced with data from an increased study population.

Indexed as

biomarkerscaninechronic valvular diseasemiRNAMMVDpredictive modeling

Identifiers

PMID39553198
PMCPMC11565599

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.