Evidence map›Paper›PMID 40745193›Full record

ArticleScientific reports2025

Profiling of the microRNA transcriptome in feline whole blood.

Åsa Ohlsson, Sofia Hanås, Bodil S Holst, Julie Lorent, Göran Andersson, Katja Höglund, Anna Tidholm, Ingrid Ljungvall, Jens Häggström

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Åsa OhlssonDepartment of Animal Biosciences, Swedish University of Agricultural Sciences, Uppsala, Sweden. asa.ohlsson@slu.se.
Sofia HanåsDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Bodil S HolstDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Julie LorentNational Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
Göran AnderssonDepartment of Animal Biosciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Katja HöglundDepartment of Animal Biosciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Anna TidholmDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Ingrid LjungvallDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Jens HäggströmDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating microRNAs (miRNAs) are potential biomarkers for numerous diseases. Characterization of the whole blood (WB) miRNA-transcriptome (miRNome) in cats is lacking, which limits the potential use of miRNAs as biomarkers for diseases such as feline cardiovascular disease. The aims of the present study were to profile and evaluate circulating miRNAs in feline WB by high-throughput sequencing of the total miRNome in WB from twelve domestic mixed breed (DOM) and Norwegian Forest (NFO) cats stringently diagnosed with or without preclinical hypertrophic cardiomyopathy (HCM). A total of 459 mature miRNAs were identified in feline WB, of which 40 were potential novel feline miRNAs. A majority, 85.3%, of the miRNAs showed sequence similarity with human miRNAs. An effect of breed was found, with up to thirteen WB miRNAs being differentially abundant between breeds. The majority of the significant breed-specific miRNAs in feline WB could be associated with regulation of haematopoietic cells. One miRNA, miR-204-5p, was potentially associated with preclinical HCM in NFO cats, but the results need to be confirmed in a larger and sex-unbiased cohort. In conclusion, here we used miRNome-sequencing to identify hundreds of circulating miRNAs in feline WB. Breed should be considered when evaluating the miRNome in feline WB.

Indexed as

Cardiomyopathy, HypertrophicCirculating MicroRNAGene Expression ProfilingMicroRNAsTranscriptomeAnimalsBiomarkersCatsFemaleHigh-Throughput Nucleotide SequencingMaleBiomarkersCirculating MicroRNAMicroRNAs

Identifiers

PMID40745193
PMCPMC12313912

What OpenQuestion holds

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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.