Evidence map›Paper›PMID 42737847›Full record

ArticleInternational journal of molecular sciences2026

Left Ventricular Molecular Signature in Chronic Aortic Regurgitation.

Bachar El Oumeiri, Laurence Dewachter, Philippe Van de Borne, Géraldine Hubesch, Pascale Jespers, Constantin Stefanidis, Kathleen Mc Entee, Frédéric Vanden Eynden

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

8 authors.

Bachar El OumeiriDepartment of Cardiac Surgery, H.U.B.-Erasme University Hospital, Route de Lennik 808, 1070 Brussels, Belgium.
Laurence DewachterLaboratory of Physiology and Pharmacology, Faculty of Medicine, Université Libre de Bruxelles, 1070 Brussels, Belgium.
Philippe Van de BorneDepartment of Cardiology, H.U.B.-Erasme University Hospital, Route de Lennik 808, 1070 Brussels, Belgium.
Géraldine HubeschLaboratory of Physiology and Pharmacology, Faculty of Medicine, Université Libre de Bruxelles, 1070 Brussels, Belgium.
Pascale JespersLaboratory of Physiology and Pharmacology, Faculty of Medicine, Université Libre de Bruxelles, 1070 Brussels, Belgium.
Constantin StefanidisDepartment of Cardiac Surgery, H.U.B.-Erasme University Hospital, Route de Lennik 808, 1070 Brussels, Belgium.
Kathleen Mc EnteeLaboratory of Physiology and Pharmacology, Faculty of Medicine, Université Libre de Bruxelles, 1070 Brussels, Belgium.
Frédéric Vanden EyndenDepartment of Cardiac Surgery, H.U.B.-Erasme University Hospital, Route de Lennik 808, 1070 Brussels, Belgium.

Funding

Foundation for Cardiac Surgery 489639
6 · The paper itself

Abstract

Molecular mechanisms underlying the progression from compensated eccentric hypertrophy to heart failure in chronic aortic regurgitation (AR) remain poorly understood. We investigated associated transcriptional changes induced by chronic volume overload in an experimental model of severe AR. AR was induced in male Wistar rats (n = 10) by retrograde aortic valve perforation and compared with age-matched control rats (n = 8). Sixty days after surgery, cardiac remodeling was evaluated by echocardiography, invasive hemodynamics and myocardial gene-expression profiling using RT-qPCR. Chronic AR induced marked left ventricular dilatation and systolic dysfunction, consistent with decompensated eccentric hypertrophy. These functional alterations were accompanied by coordinated transcriptional changes involving pathways related to apoptosis, oxidative balance, metabolic regulation and calcium handling. AR hearts exhibited an increased

Indexed as

Aortic Valve InsufficiencyHeart VentriclesAnimalsApoptosisChronic DiseaseDisease Models, AnimalGene Expression ProfilingGene Expression RegulationMaleMyocardiumOxidative StressRatsRats, WistarSarcoplasmic Reticulum Calcium-Transporting ATPasesTranscriptomeVentricular RemodelingSarcoplasmic Reticulum Calcium-Transporting ATPasesaortic regurgitationcalcium handlinggene expressionkallikrein–kinin systemleft ventricular decompensationmetabolic remodelingoxidative stress

Identifiers

PMID42737847
PMCPMC13566205

What Socratic holds

Textmetadata
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 Socratic graph.