Evidence map›Paper›PMID 26516182›Full record

ReviewHeart (British Cardiac Society)2016

Cellular and molecular basis of RV hypertrophy in congenital heart disease.

D Iacobazzi, M-S Suleiman, M Ghorbel, S J George, M Caputo, R M Tulloh

Open access · hybridAbstract readReview
In one paragraph

Review in Heart (British Cardiac Society), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Immature and mature myocardium in the pathophysiology of hypertrophic cardiomyopathy.Journal of molecular and cellular cardiology plus · 2026
    Review
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  16. Role of Inflammatory Cell Subtypes in Heart Failure.Journal of immunology research · 2019
    Review
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  18. Article
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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

6 authors at 1 institution in 1 country.

D IacobazziSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK.
M-S SuleimanSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK.
M GhorbelSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK.
S J GeorgeSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK.
M CaputoSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK Department of Congenital Heart Disease, Bristol Royal Hospital for Children, Bristol, UK.
R M TullohSchool of Clinical Sciences, Bristol Royal Infirmary, Bristol, UK Department of Congenital Heart Disease, Bristol Royal Hospital for Children, Bristol, UK.
Bristol Royal Infirmary · GB

Funding

British Heart Foundation PG/15/33/31394Department of Health PB-PG-0711-25145
6 · The paper itself

Abstract

RV hypertrophy (RVH) is one of the triggers of RV failure in congenital heart disease (CHD). Therefore, improving our understanding of the cellular and molecular basis of this pathology will help in developing strategic therapeutic interventions to enhance patient benefit in the future. This review describes the potential mechanisms that underlie the transition from RVH to RV failure. In particular, it addresses structural and functional remodelling that encompass contractile dysfunction, metabolic changes, shifts in gene expression and extracellular matrix remodelling. Both ischaemic stress and reactive oxygen species production are implicated in triggering these changes and will be discussed. Finally, RV remodelling in response to various CHDs as well as the potential role of biomarkers will be addressed.

Indexed as

Ventricular Function, RightVentricular RemodelingAnimalsBiomarkersDisease ProgressionGene Expression RegulationGenomicsHeart Defects, CongenitalHeart FailureHumansHypertrophy, Right VentricularMicroRNAsMyocardial ContractionMyocardiumProteomicsRisk FactorsBiomarkersMicroRNAs

Identifiers

PMID26516182
PMCPMC4717403
OpenAlexW2164842229

What OpenQuestion holds

Textmetadata
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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.