Evidence map›Paper›PMID 40859622›Full record

ArticleInflammatory bowel diseases2025

Tissue MicroRNA Expression Signatures as Diagnostic Biomarkers and Predictors of Residual Disease Activity and Relapse in Treatment-Naïve Pediatric Inflammatory Bowel Disease.

Tereza Deissova, Dagmar Al Tukmachi, Lenka Radova, Julia Bohosova, Tana Machackova, Leos Kren, Matej Hrunka, Tereza Pinkasova, Martina Ambrozova, Jiri Sana and 2 more

Abstract read
In one paragraph

Article in Inflammatory bowel diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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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

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2 · The registry

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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
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4 · The record

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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.

Tereza DeissovaDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0003-4853-1233
Dagmar Al TukmachiDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-1320-8180
Lenka RadovaDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0001-8103-148X
Julia BohosovaDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0003-1286-1118
Tana MachackovaDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0001-5055-7147
Leos KrenDepartment of Pathology, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-9509-1552
Matej HrunkaDepartment of Pediatrics, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-8154-1567
Tereza PinkasovaDepartment of Pediatrics, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID 0009-0008-6949-8237
Martina AmbrozovaDepartment of Pediatrics, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID 0009-0000-2846-4673
Jiri SanaDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0003-1610-2215
Ondrej SlabyDepartment of Biology, Faculty of Medicine and Central European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-8450-0584
Petr JabandzievDepartment of Pediatrics, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-4094-2364

Funding

Ministry of Health of the Czech Republic NU21-07-00285
6 · The paper itself

Abstract

backgroundIdentifying novel diagnostic and prognostic biomarkers for pediatric inflammatory bowel diseases (PIBD), including Crohn's disease (pCD) and ulcerative colitis (pUC), is essential for enhancing treatment outcomes. MicroRNAs (miRNAs) have been recognized for their broader relevance in PIBD pathogenesis. This study investigates their diagnostic potential and clinical utility in PIBD.

methodsThis prospective, monocentric study, with retrospective validation, involved 119 PIBD patients (58 pCD, 61 pUC) and 39 non-IBD controls. Small RNA next-generation sequencing was performed on fresh-frozen gut biopsies, targeting histopathologically confirmed inflamed areas. Twenty-five dysregulated miRNA candidates were validated via RT-qPCR in formalin-fixed, paraffin-embedded gut biopsies. Logistic regression was used to establish diagnostic and prognostic miRNA expression signatures.

resultsA diagnostic signature of 5 miRNAs (miR-223-3p, miR-34a-5p, miR-194-5p, miR-215-5p, miR-338-3p) distinguished pCD from non-IBD with 96.49% accuracy. Two miRNAs (miR-223-3p, miR-194-5p) differentiated pUC from non-IBD with 100% accuracy, and miR-215-5p distinguished pCD from pUC specimens with 83.54% accuracy. For treatment-naïve pCD patients, 7 miRNAs predicted residual disease activity at 3 months with 100% accuracy. Additionally, a distinct signature predicted the risk of relapse within 12 months with an accuracy of 84.21%.

conclusionsIn this study, we have established tissue miRNA expression signatures with significant diagnostic and prognostic potential for use in PIBD. These findings aid in stratifying disease severity and risk, paving the way for more precise and personalized management of pediatric IBD.

Indexed as

BiomarkersColitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesMicroRNAsAdolescentCase-Control StudiesChildChild, PreschoolFemaleFollow-Up StudiesGene Expression ProfilingHumansMalePrognosisProspective StudiesBiomarkersMicroRNAsinflammatory bowel diseasemicroRNA markerspediatric

Identifiers

PMID40859622
PMCPMC12638064

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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.