Evidence map›Paper›PMID 23355885›Full record

Trial reportPloS one2013

Gender differences in electrophysiological gene expression in failing and non-failing human hearts.

Christina M Ambrosi, Kathryn A Yamada, Jeanne M Nerbonne, Igor R Efimov

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.8field-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

33 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Connexin43 Deficiency Leads to Ventricular Arrhythmias by Reprogramming Proline Metabolism.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Enhanced CaJACC. Clinical electrophysiology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. ESC working group on cardiac cellular electrophysiology position paper: relevance, opportunities, and limitations of experimental models for cardiac electrophysiology research.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2021
    Review
  14. Review
  15. Article
  16. Circadian Pattern of Ion Channel Gene Expression in Failing Human Hearts.Circulation. Arrhythmia and electrophysiology · 2021
    Article
  17. Review
  18. BlindedFrontiers in pharmacology · 2019
    Article
  19. Review
  20. Sex Differences in Metabolic Cardiomyopathy.Cardiovascular research · 2017
    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

4 authors at 1 institution in 1 country.

Christina M AmbrosiDepartment of Biomedical Engineering, Washington University in St. Louis, St. Louis, Missouri, United States of America.
Kathryn A Yamada
Jeanne M Nerbonne
Igor R Efimov
Washington University in St. Louis · US

Funding

ARRHYTHMOGENIC REMODELING IN HUMAN HEART FAILURER01HL114395 · NHLBI · WASHINGTON UNIVERSITY · PI EFIMOV, IGOR R · 2012 to 2015
$2.1M
STRUCTURE/FUNCTION OF THE PACEMAKING AND CONDUCTION SYSTEM OF THE HEARTR01HL085369 · NHLBI · WASHINGTON UNIVERSITY · PI EFIMOV, IGOR R · 2008 to 2011
$1.5M
NHLBI NIH HHS R01 HL085369NHLBI NIH HHS R01-HL085369NHLBI NIH HHS R01 HL114395NHLBI NIH HHS R01-HL114395
6 · The paper itself

Abstract

The increasing availability of human cardiac tissues for study are critically important in increasing our understanding of the impact of gender, age, and other parameters, such as medications and cardiac disease, on arrhythmia susceptibility. In this study, we aimed to compare the mRNA expression of 89 ion channel subunits, calcium handling proteins, and transcription factors important in cardiac conduction and arrhythmogenesis in the left atria (LA) and ventricles (LV) of failing and nonfailing human hearts of both genders. Total RNA samples, prepared from failing male (n = 9) and female (n = 7), and from nonfailing male (n = 9) and female (n = 9) hearts, were probed using custom-designed Taqman gene arrays. Analyses were performed to explore the relationships between gender, failure state, and chamber expression. Hierarchical cluster analysis revealed chamber specific expression patterns, but failed to identify disease- or gender-dependent clustering. Gender-specific analysis showed lower expression levels in transcripts encoding for K(v)4.3, KChIP2, K(v)1.5, and K(ir)3.1 in the failing female as compared with the male LA. Analysis of LV transcripts, however, did not reveal significant differences based on gender. Overall, our data highlight the differential expression and transcriptional remodeling of ion channel subunits in the human heart as a function of gender and cardiac disease. Furthermore, the availability of such data sets will allow for the development of disease-, gender-, and, most importantly, patient-specific cardiac models, with the ability to utilize such information as mRNA expression to predict cardiac phenotype.

Indexed as

Electrophysiological PhenomenaGene Expression RegulationHeart FailureSex CharacteristicsAdultAgedFemaleGene Expression ProfilingHumansMaleMiddle AgedModels, CardiovascularMuscle ProteinsMyocardiumMuscle Proteins

Identifiers

PMID23355885
PMCPMC3552854
OpenAlexW2011730969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.