Evidence map›Paper›PMID 39596076›Full record

ReviewInternational journal of molecular sciences2024

Epigenetics in Heart Failure.

Jamie Sin Ying Ho, Eric Jou, Pek-Lan Khong, Roger S Y Foo, Ching-Hui Sia

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Nuclear m6A Methylase METTL3 Drives Production of ITGβ4E to Exacerbate Heart Failure via SRSF3-Mediated Alternative Splicing of ITGβ4.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

5 authors.

Jamie Sin Ying HoDepartment of Cardiology, National University Heart Centre, Singapore 119228, Singapore.
Eric JouDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.
Pek-Lan KhongDepartment of Diagnostic Imaging, National University Hospital, National University Health System, Singapore 119074, Singapore.ORCID 0000-0002-9280-6778
Roger S Y FooDepartment of Cardiology, National University Heart Centre, Singapore 119228, Singapore.
Ching-Hui SiaDepartment of Cardiology, National University Heart Centre, Singapore 119228, Singapore.ORCID 0000-0002-2764-2869

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure is a clinical syndrome with rising global incidence and poor prognosis despite improvements in medical therapy. There is increasing research interest in epigenetic therapies for heart failure. Pathological cardiac remodelling may be driven by stress-activated cardiac signalling cascades, and emerging research has shown the involvement of epigenetic signals that regulate transcriptional changes leading to heart failure. In this review, we appraise the current evidence for the role of epigenetic modifications in heart failure. These include DNA methylation and histone modifications by methylation, acetylation, phosphorylation, ubiquitination and sumoylation, which are critical processes that establish an epigenetic pattern and translate environmental stress into genetic expression, leading to cardiac remodeling. We summarize the potential epigenetic therapies currently in development, including the limited clinical trials of epigenetic therapies in heart failure. The dynamic changes in the epigenome in the disease process require further elucidation, and so does the impact of this process on the development of therapeutics. Understanding the role of epigenetics in heart failure may pave the way for the identification of novel biomarkers and molecular targets, and facilitate the development of personalized therapies for this important condition.

Indexed as

DNA MethylationEpigenesis, GeneticHeart FailureAnimalsHistonesHumansHistonesDNA methylationepigenetic modificationheart failurehistone modificationspersonalized medicine

Identifiers

PMID39596076
PMCPMC11593553

What OpenQuestion holds

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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.