Evidence map›Paper›PMID 28850583›Full record

ArticlePloS one2017

Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease.

Kolsoum InanlooRahatloo, Grace Liang, Davis Vo, Antje Ebert, Ivy Nguyen, Patricia K Nguyen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  5. Review
  6. Review
  7. Article
  8. New role for cardiomyocytebioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Seeking clarity on sex differences in cardiovascular complications of Down syndrome.American journal of physiology. Heart and circulatory physiology · 2023
    Article
  11. Article
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  13. Article
  14. Article
  15. Review
  16. Article
  17. Sex-Related Differences in Genetic Cardiomyopathies.Journal of the American Heart Association · 2022
    Review
  18. Review
  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

6 authors at 1 institution in 2 countries.

Kolsoum InanlooRahatlooStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.ORCID http://orcid.org/0000-0002-5316-8259
Grace LiangStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.
Davis VoStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.
Antje EbertStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.
Ivy NguyenStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.ORCID http://orcid.org/0000-0001-5612-8159
Patricia K NguyenStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, United States of America.
Cardiovascular Institute of the South · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sex differences in the development of the normal heart and the prevalence of cardiomyopathies have been reported. The molecular basis of these differences remains unclear. Sex differences in the human heart might be related to patterns of gene expression. Recent studies have shown that sex specific differences in gene expression in tissues including the brain, kidney, skeletal muscle, and liver. Similar data is limited for the heart. Herein we address this issue by analyzing donor and post-mortem adult human heart samples originating from 46 control individuals to study whole-genome gene expression in the human left ventricle. Using data from the genotype tissue expression (GTEx) project, we compared the transcriptome expression profiles of male and female hearts. We found that genes located on sex chromosomes were the most abundant ones among the sexually dimorphic genes. The majority of differentially expressed autosomal genes were those involved in the regulation of inflammation, which has been found to be an important contributor to left ventricular remodeling. Specifically, genes on autosomal chromosomes encoding chemokines with inflammatory functions (e.g. CCL4, CX3CL1, TNFAIP3) and a gene that regulates adhesion of immune cells to the endothelium (e.g., VCAM1) were identified with sex-specific expression levels. This study underlines the relevance of sex as an important modifier of cardiac gene expression. These results have important implications in the understanding of the differences in the physiology of the male and female heart transcriptome and how they may lead to different sex specific difference in human cardiac health and its control.

Indexed as

Gene ExpressionTissue DonorsTranscriptomeAdultAgedChemokinesFemaleGene Expression ProfilingHumansMaleMiddle AgedMyocardiumSex CharacteristicsChemokines

Identifiers

PMID28850583
PMCPMC5574577
OpenAlexW2751978230

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.