Evidence map›Paper›PMID 28130338›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2017

Exosomes from pediatric dilated cardiomyopathy patients modulate a pathological response in cardiomyocytes.

Xuan Jiang, Juliana Sucharov, Brian L Stauffer, Shelley D Miyamoto, Carmen C Sucharov

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Circulating and Cardiac Tissue miRNAs in Children with Dilated Cardiomyopathy.Journal of cardiovascular development and disease · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Influence of microRNAs and exosomes in muscle health and diseases.Journal of muscle research and cell motility · 2020
    Article
  18. Article
  19. Review
  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

5 authors at 4 institutions in 1 country.

Xuan JiangDivision of Cardiology, Department of Medicine, University of Colorado Denver, Aurora, Colorado.
Juliana SucharovDivision of Cardiology, Department of Medicine, University of Colorado Denver, Aurora, Colorado.
Brian L StaufferDivision of Cardiology, Department of Medicine, University of Colorado Denver, Aurora, Colorado.ORCID http://orcid.org/0000-0003-3418-7750
Shelley D MiyamotoDepartment of Pediatrics, University of Colorado School of Medicine, Children's Hospital, Aurora, Colorado.
Carmen C SucharovDivision of Cardiology, Department of Medicine, University of Colorado Denver, Aurora, Colorado; kika.sucharov@ucdenver.edu.
University of Colorado Denver · USChildren's Hospital Colorado · USDenver Health Medical Center · USUniversity of Colorado Boulder · US

Funding

Translational Pulmonary Vascular Biology ProgramT32HL007171 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Sonia Castro Flores, Tim Lahm · 1985 to 2026
$9.4M
Molecular and Functional Mechanisms of Pediatric Heart FailureR01HL107715 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STAUFFER, BRIAN L · 2012 to 2016
$2.8M
NHLBI NIH HHS R01 HL107715NHLBI NIH HHS T32 HL007171
6 · The paper itself

Abstract

Stimulation of the renin-angiotensin-aldosterone system (RAAS) and β-adrenergic receptors plays an important role in adult heart failure (HF). Despite the demonstrated benefits of RAAS inhibition and β-adrenergic receptor blockade in adult HF patients, no substantial improvement in survival rate has been observed in children with HF. This suggests that the underlying disease mechanism is uniquely regulated in pediatric HF. Here, we show that treatment of human-induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) and neonatal rat ventricular myocytes (NRVMs) with serum from pediatric dilated cardiomyopathy (DCM) patients induces pathological changes in gene expression, which occur independently of the RAAS and adrenergic systems, suggesting that serum circulating factors play an important role in cardiac remodeling. Furthermore, exosomes purified from DCM serum induced pathological changes in gene expression in NRVMs and iPSC-CMs. Our results suggest that DCM serum exosomes mediate pathological responses in cardiomyocytes and may propagate the pediatric HF disease process, representing a potential novel therapeutic target specific to this population.

Indexed as

AnimalsAnimals, NewbornCardiomyopathy, DilatedCells, CulturedCell SizeChildChild, PreschoolExosomesFemaleGene ExpressionHeart VentriclesHumansInduced Pluripotent Stem CellsInfantMaleMyocytes, Cardiaccellular hypertrophyexosomesfetal gene programpediatric dilated cardiomyopathy

Identifiers

PMID28130338
PMCPMC5407162
OpenAlexW2579928900

What OpenQuestion holds

Textmetadata
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.