Evidence map›Paper›PMID 32664951›Full record

ArticleClinical epigenetics2020

H3K27ac acetylome signatures reveal the epigenomic reorganization in remodeled non-failing human hearts.

Jiayi Pei, Magdalena Harakalova, Thomas A Treibel, R Thomas Lumbers, Bastiaan J Boukens, Igor R Efimov, Jip T van Dinter, Arantxa González, Begoña López, Hamid El Azzouzi and 17 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2020. 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
4.1field-weighted citation impact, top 6% 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, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Cardiac epigenome in heart development and disease.Nature reviews. Cardiology · 2026
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  8. Participation of transgender and gender diverse persons in cardiovascular clinical trials.American heart journal plus : cardiology research and practice · 2024
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  11. Review
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  14. Article
  15. Sex-Related Effects on Cardiac Development and Disease.Journal of cardiovascular development and disease · 2022
    Review
  16. Oestrogenic Regulation of Mitochondrial Dynamics.International journal of molecular sciences · 2022
    Review
  17. Article
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  19. Article
  20. Article
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

27 authors at 8 institutions in 5 countries.

Jiayi PeiDepartment of Nephrology and Hypertension, DIGD, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Magdalena HarakalovaDepartment of Cardiology, Division Heart & Lungs, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Thomas A TreibelInstitute of Cardiovascular Science, University College London, London, UK.
R Thomas LumbersInstitute of Cardiovascular Science, University College London, London, UK.
Bastiaan J BoukensDepartment of Medical Biology, AMC, Amsterdam, Netherlands.
Igor R EfimovDepartment of Biomedical Engineering, GWU, Washington, D.C, USA.
Jip T van DinterDepartment of Cardiology, Division Heart & Lungs, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Arantxa GonzálezProgram of Cardiovascular Diseases, CIMA Universidad de Navarra and IdiSNA, Pamplona, Spain.
Begoña LópezProgram of Cardiovascular Diseases, CIMA Universidad de Navarra and IdiSNA, Pamplona, Spain.
Hamid El AzzouziDepartment of Cardiology, Division Heart & Lungs, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Noortje van den DungenLaboratory of Clinical Chemistry and Hematology, UMC Utrecht, Utrecht, Netherlands.
Christian G M van DijkDepartment of Nephrology and Hypertension, DIGD, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Merle M KrebberDepartment of Nephrology and Hypertension, DIGD, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Hester M den RuijterDepartment of Experimental Cardiology, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Gerard PasterkampLaboratory of Clinical Chemistry and Hematology, UMC Utrecht, Utrecht, Netherlands.
Dirk J DunckerDivision of Experimental Cardiology, Department of Cardiology, Erasmus University Medical Center, Rotterdam, Netherlands.
Edward E S NieuwenhuisDivision of Paediatrics, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Roel de WegerDepartment of Pathology, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Manon M HuibersDepartment of Pathology, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Aryan VinkDepartment of Pathology, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Jason H MooreInstitute for Biomedical Informatics, UPENN, Philadelphia, USA.
James C MoonInstitute of Cardiovascular Science, University College London, London, UK.
Marianne C VerhaarDepartment of Nephrology and Hypertension, DIGD, UMC Utrecht, University of Utrecht, Utrecht, Netherlands.
Georgios KararigasCharité - Universitätsmedizin Berlin, and DZHK (German Centre for Cardiovascular Research), partner site, Berlin, Germany.
Michal MokryRegenerative Medicine Utrecht (RMU), UMC Utrecht, University of Utrecht, Utrecht, Netherlands. M.Mokry@umcutrecht.nl.
Folkert W AsselbergsDepartment of Cardiology, Division Heart & Lungs, UMC Utrecht, University of Utrecht, Utrecht, Netherlands. F.W.Asselbergs@umcutrecht.nl.
Caroline ChengDepartment of Nephrology and Hypertension, DIGD, UMC Utrecht, University of Utrecht, Utrecht, Netherlands. K.L.Cheng-2@umcutrecht.nl.ORCID 0000-0001-9026-391X
Utrecht University · NLUniversity College London · GBInstituto de Salud Carlos III · ESErasmus MC · NLGerman Centre for Cardiovascular Research · DEGW Medical Faculty Associates · USPhiladelphia University · USUniversity of Applied Sciences Utrecht · NL

Funding

British Heart Foundation FS/19/35/34374Department of Health DRF-2013-06-102Medical Research Council MR/S003754/1
6 · The paper itself

Abstract

backgroundH3K27ac histone acetylome changes contribute to the phenotypic response in heart diseases, particularly in end-stage heart failure. However, such epigenetic alterations have not been systematically investigated in remodeled non-failing human hearts. Therefore, valuable insight into cardiac dysfunction in early remodeling is lacking. This study aimed to reveal the acetylation changes of chromatin regions in response to myocardial remodeling and their correlations to transcriptional changes of neighboring genes.

resultsWe detected chromatin regions with differential acetylation activity (DARs; P

conclusionsOur study reveals extensive novel insight on myocardial remodeling at the DNA regulatory level. Differences between the acetylation level and the transcriptional level of cell-type-specific markers suggest additional mechanism(s) between acetylome and transcriptome. By integrating these two layers of epigenetic profiles, we further provide promising TF-encoding genes that could serve as master regulators of myocardial remodeling. Combined, our findings highlight the important role of chromatin regulatory signatures in understanding disease etiology.

Indexed as

AcetylationAdultCase-Control StudiesChromatinEpigenomicsFemaleHeart FailureHistonesHumansMaleMyocardiumMyocytes, CardiacRNA, MessengerRNA Polymerase IITranscription FactorsTranscriptomeChromatinHistonesRNA, MessengerRNA Polymerase IITranscription FactorsHistone acetylationMyocardial remodelingTranscription factorTranscriptome

Identifiers

PMID32664951
PMCPMC7362435
OpenAlexW3043272558

What OpenQuestion holds

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Registered trials

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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.