Evidence map›Paper›PMID 23341106›Full record

ArticleEMBO molecular medicine2013

Alterations in cardiac DNA methylation in human dilated cardiomyopathy.

Jan Haas, Karen S Frese, Yoon Jung Park, Andreas Keller, Britta Vogel, Anders M Lindroth, Dieter Weichenhan, Jennifer Franke, Simon Fischer, Andrea Bauer and 18 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 3 pooled it
12.1field-weighted citation impact, top 1% 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

115 citing papers in PubMed, 3 syntheses or guidelines pooled it, 242 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.Clinical research in cardiology : official journal of the German Cardiac Society · 2017
    Pooled it
  4. Article
  5. Cardiac epigenome in heart development and disease.Nature reviews. Cardiology · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Regulatory roles of PIWI-interacting RNAs in cardiovascular disease.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Using Omics to Identify Novel Therapeutic Targets in Heart Failure.Circulation. Genomic and precision medicine · 2024
    Review
  20. Review

55 more citing papers are in PubMed but not listed here.

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

28 authors at 7 institutions in 2 countries.

Jan HaasDepartment of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
Karen S Frese
Yoon Jung Park
Andreas Keller
Britta Vogel
Anders M Lindroth
Dieter Weichenhan
Jennifer Franke
Simon Fischer
Andrea Bauer
Sabine Marquart
Farbod Sedaghat-Hamedani
Elham Kayvanpour
Doreen Köhler
Nadine M Wolf
Sarah Hassel
Rouven Nietsch
Thomas Wieland
Philipp Ehlermann
Jobst-Hendrik Schultz
Andreas Dösch
Derliz Mereles
Stefan Hardt
Johannes Backs
Jörg D Hoheisel
Christoph Plass
Hugo A Katus
Benjamin Meder
Heidelberg University · DEEpigenomics (Germany) · DEGerman Cancer Research Center · DEUniversity Hospital Heidelberg · DEGerman Centre for Cardiovascular Research · DESaarland University · DEUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dilated cardiomyopathies (DCM) show remarkable variability in their age of onset, phenotypic presentation, and clinical course. Hence, disease mechanisms must exist that modify the occurrence and progression of DCM, either by genetic or epigenetic factors that may interact with environmental stimuli. In the present study, we examined genome-wide cardiac DNA methylation in patients with idiopathic DCM and controls. We detected methylation differences in pathways related to heart disease, but also in genes with yet unknown function in DCM or heart failure, namely Lymphocyte antigen 75 (LY75), Tyrosine kinase-type cell surface receptor HER3 (ERBB3), Homeobox B13 (HOXB13) and Adenosine receptor A2A (ADORA2A). Mass-spectrometric analysis and bisulphite-sequencing enabled confirmation of the observed DNA methylation changes in independent cohorts. Aberrant DNA methylation in DCM patients was associated with significant changes in LY75 and ADORA2A mRNA expression, but not in ERBB3 and HOXB13. In vivo studies of orthologous ly75 and adora2a in zebrafish demonstrate a functional role of these genes in adaptive or maladaptive pathways in heart failure.

Indexed as

DNA MethylationEpigenesis, GeneticAdultAgedAnimalsAntigens, CDBiopsyCardiomyopathy, DilatedCase-Control StudiesCluster AnalysisFemaleGene Expression RegulationGene Knockdown TechniquesGenetic Predisposition to DiseaseHEK293 CellsHumansAntigens, CDDEC-205 receptorLectins, C-TypeMinor Histocompatibility AntigensReceptor, Adenosine A2AReceptors, Cell SurfaceRNA, MessengerZebrafish Proteins

Identifiers

PMID23341106
PMCPMC3598081
OpenAlexW1815197835

What OpenQuestion holds

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LicenceCC BY
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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.