Evidence map›Paper›PMID 18022084›Full record

ArticleThe Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation2007

Assist devices fail to reverse patterns of fetal gene expression despite beta-blockers.

Brian D Lowes, Ronald Zolty, Simon F Shakar, Andreas Brieke, Norman Gray, Michael Reed, Mihail Calalb, Wayne Minobe, JoAnn Lindenfeld, Eugene E Wolfel and 3 more

Open access · greenAbstract readControlled Clinical Trial
In one paragraph

Article in The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  5. DNA methylation reprograms cardiac metabolic gene expression in end-stage human heart failure.American journal of physiology. Heart and circulatory physiology · 2019
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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

13 authors at 1 institution in 1 country.

Brian D LowesDivision of Cardiology, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA. Brian.Lowes@UCHSC.edu
Ronald Zolty
Simon F Shakar
Andreas Brieke
Norman Gray
Michael Reed
Mihail Calalb
Wayne Minobe
JoAnn Lindenfeld
Eugene E Wolfel
Mark Geraci
Michael R Bristow
Joseph Cleveland
University of Colorado Health · US

Funding

Gene expression profiles in the failing human heartK23HL068875 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI LOWES, BRIAN D · 2003 to 2007
$653k
NHLBI NIH HHS K23 HL068875
6 · The paper itself

Abstract

backgroundHeart failure is associated with reversal to a fetal gene expression pattern of contractile and metabolic genes. Substantial recovery of ventricular function with assist devices is rare. Our goal was to evaluate the effects of assist devices on fetal gene expression and hypoxia inducible factor-1 alpha (HIF-1 alpha), a transcriptional factor in hypoxic signaling.

methodsHuman heart tissue was obtained from the left ventricular apex at the time of assist device implantation and again from the left ventricular free wall during cardiac transplantation. Non-failing tissue was obtained from unused hearts from human donors. Gene expression was measured with the Affymetrix 133 plus 2 Array. HIF-1 alpha was measured by Western blotting with commercially available antibodies.

resultsHeart failure was associated with a decrease in alpha-myosin heavy chain and sarcoplasmic reticulum-Ca(2+) adenosine triphosphatase messenger RNA expression along with an increase in skeletal tropomyosin. This pattern persisted after assist device therapy. Heart failure was also associated with abnormalities in regulatory metabolic genes including glucose transporter 1 (GLUT1). These patterns also persisted after assist device therapy despite a reduction in atrial natriuretic peptide expression and normalization of HIF-1 alpha.

conclusionsFailure of assist devices to produce sustained recovery of myocardial contractile function may be due in part to persistent fetal transcriptional patterns of contractile and metabolic genes.

Indexed as

Gene Expression ProfilingHeart-Assist DevicesAdrenergic beta-AntagonistsAdultAngiotensin-Converting Enzyme InhibitorsAtrial Natriuretic FactorGene Expression RegulationGene Expression Regulation, DevelopmentalGlucose Transporter Type 1Heart FailureHumansHypoxia-Inducible Factor 1, alpha SubunitMiddle AgedMineralocorticoid Receptor AntagonistsMyocardial ContractionMyosin Heavy ChainsAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAtrial Natriuretic FactorGlucose Transporter Type 1HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMineralocorticoid Receptor AntagonistsMyosin Heavy ChainsProtein Serine-Threonine KinasesPyruvate Dehydrogenase Acetyl-Transferring KinaseSarcoplasmic Reticulum Calcium-Transporting ATPasesSLC2A1 protein, humanTropomyosin

Identifiers

PMID18022084
PMCPMC2768343
OpenAlexW2055606032

What OpenQuestion holds

Textmetadata
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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.