Evidence map›Paper›PMID 42850495›Full record

ArticleJournal of cardiovascular translational research2026

Higher Myocardial miR-1-3p, miR-30a-5p, miR-34a-5p, and Lower miR208a-3p Levels are Associated with Lower Age at the Time of Heart Transplantation.

Vid Mirosevic, Tanja Blagus, Tomo Svagusa, Ana Livun, Petra Bakovic, Ana Sepac, Ana Kulic, Vita Dolzan, Filip Sedlic

Abstract read
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In one paragraph

Article in Journal of cardiovascular translational research, 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

9 authors.

Vid MirosevicDepartment of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia.
Tanja BlagusPharmacogenetics Laboratory, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, 1000, Slovenia.
Tomo SvagusaDepartment of Cardiovascular Diseases, Dubrava University Hospital, Zagreb, Croatia.
Ana LivunDepartment of Scientific Research and Translational Medicine, University Hospital Dubrava, Zagreb, 10000, Croatia.
Petra BakovicDepartment of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia.
Ana SepacDepartment of Pathology, School of Medicine, University of Zagreb, Salata 10, Zagreb, 10 000, Croatia. ana.sepac@mef.hr.
Ana KulicDepartment of Oncology, University Hospital Centre Zagreb, Zagreb, Croatia.
Vita DolzanPharmacogenetics Laboratory, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, 1000, Slovenia.
Filip SedlicDepartment of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia.

Funding

Javna Agencija za Raziskovalno Dejavnost RS P1-0170Ministry of Science and Technology, Croatia 10106-25-3006
6 · The paper itself

Abstract

Expression of microRNAs (miR-1-3p, miR-21-3p, miR-30a-5p, miR-34a-5p, miR-133a-3p, miR-208a-3p, and miR-423-5p) and mitochondrial unfolded protein response (UPRmt) genes (HSPA9, HSPD1, LONP1, OMA1, and YME1L) was investigated by qRT-PCR in six controls and 65 failing human hearts (33 ischemic cardiomyopathy (ICM), 28 dilated cardiomyopathy (DCM), 2 hypertrophic cardiomyopathy, and 1 non-compaction and restrictive cardiomyopathy each). Failing hearts had higher expression of miR-208a-3p, HSPA9, HSPD1, OMA1, YME1L and lower miR-1-3p expression compared to controls. Patients with higher miR-1-3p, miR-30a-5p, miR-34a-5p, (miR-423-5p exhibited a trend) and lower miR-208a-3p expression underwent heart transplantation or LVAD implantation earlier in life. DCM group had higher expression of miR-1-3p, miR-30a-5p, HSPD1, and LONP1 compared to the ICM group. Thus, myocardial expression of miR-1-3p, miR-30a-5p, miR-34a-5p, and miR-208a-3p could be associated with the HF progression; miR-208a-3p, HSPA9, HSPD1, OMA1, YME1L, and miR-1-3p could discriminate HF form control; and miR-1-3p, miR-30a-5p, HSPD1, and LONP1 could discriminate DCM from ICM.

Indexed as

Heart FailureHeart TransplantationMicroRNAsMyocardiumAdultAgedAge FactorsCase-Control StudiesFemaleHumansMaleMiddle AgedTime FactorsUnfolded Protein ResponseMicroRNAsMIRN208 microRNA, humanMIRN30b microRNA, humanMIRN34 microRNA, humanCardiomyopathyHeart failureMiRNAMitochondrial unfolded protein responseMyocardium

Identifiers

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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.