Evidence map›Paper›PMID 23437060›Full record

ArticlePloS one2013

Intravenous glial growth factor 2 (GGF2) isoform of neuregulin-1β improves left ventricular function, gene and protein expression in rats after myocardial infarction.

Michael F Hill, Amish V Patel, Abigail Murphy, Holly M Smith, Cristi L Galindo, Laura Pentassuglia, Xuyang Peng, Carrie G Lenneman, Oghenerukevwe Odiete, David B Friedman and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.6field-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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

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  18. New medical therapies for heart failure.Nature reviews. Cardiology · 2015
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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

21 authors at 2 institutions in 1 country.

Michael F HillDivision of Cardiovascular Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Amish V Patel
Abigail Murphy
Holly M Smith
Cristi L Galindo
Laura Pentassuglia
Xuyang Peng
Carrie G Lenneman
Oghenerukevwe Odiete
David B Friedman
Marvin W Kronenberg
Siyuen Zheng
Zhongming Zhao
Yanna Song
Frank E Harrell
Maya Srinivas
Anindita Ganguly
Jennifer Iaci
Tom J Parry
Anthony O Caggiano
Douglas B Sawyer
Vanderbilt University Medical Center · USAcorda Therapeutics (United States) · US

Funding

Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Optimizing Cardiovascular Stem Cells for Cardiac Repair and RegenerationU01HL100398 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HATZOPOULOS, ANTONIS · 2009 to 2015
$8.0M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
Role of Neuregulin/erbB Signaling in the Adult HeartR01HL068144 · NHLBI · VANDERBILT UNIVERSITY · PI SAWYER, DOUGLAS B · 2001 to 2009
$2.5M
Recombinant Neuregulin for the treatment of Heart FailureP20HL101425 · NHLBI · VANDERBILT UNIVERSITY · PI BROWN, NANCY J., CAGGIANO, ANTHONY O · 2010 to 2011
$1.3M
NHLBI NIH HHS P20 HL101425NHLBI NIH HHS R01 HL068144NHLBI NIH HHS U01 HL100398NIDDK NIH HHS DK59637NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

aimsRecombinant Neuregulin (NRG)-1β has multiple beneficial effects on cardiac myocytes in culture, and has potential as a clinical therapy for heart failure (HF). A number of factors may influence the effect of NRG-1β on cardiac function via ErbB receptor coupling and expression. We examined the effect of the NRG-1β isoform, glial growth factor 2 (GGF2), in rats with myocardial infarction (MI) and determined the impact of high-fat diet as well as chronicity of disease on GGF2 induced improvement in left ventricular systolic function. Potential mechanisms for GGF2 effects on the remote myocardium were explored using microarray and proteomic analysis. METHODS AND

resultsRats with MI were randomized to receive vehicle, 0.625 mg/kg, or 3.25 mg/kg GGF2 in the presence and absence of high-fat feeding beginning at day 7 post-MI and continuing for 4 weeks. Residual left ventricular (LV) function was improved in both of the GGF2 treatment groups compared with the vehicle treated MI group at 4 weeks of treatment as assessed by echocardiography. High-fat diet did not prevent the effects of high dose GGF2. In experiments where treatment was delayed until 8 weeks after MI, high but not low dose GGF2 treatment was associated with improved systolic function. mRNA and protein expression analysis of remote left ventricular tissue revealed a number of changes in myocardial gene and protein expression altered by MI that were normalized by GGF2 treatment, many of which are involved in energy production.

conclusionsThis study demonstrates that in rats with MI induced systolic dysfunction, GGF2 treatment improves cardiac function. There are differences in sensitivity of the myocardium to GGF2 effects when administered early vs. late post-MI that may be important to consider in the development of GGF2 in humans.

Indexed as

AnimalsDiet, High-FatElectrocardiographyFibrosisGene Expression RegulationGlucoseHeart VentriclesHumansInjections, IntravenousMaleMyocardial InfarctionMyocardiumNeuregulin-1Organ SizeOxidative StressPositron-Emission TomographyGlucoseNeuregulin-1neuregulin betaProtein IsoformsProteomeReceptor Protein-Tyrosine Kinases

Identifiers

PMID23437060
PMCPMC3578842
OpenAlexW2085374859

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Registered trials

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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.