Evidence map›Paper›PMID 20719564›Full record

ArticleHeart, lung & circulation2010

Acute myocardial rescue with endogenous endothelial progenitor cell therapy.

Pavan Atluri, Corinna M Panlilio, George P Liao, William Hiesinger, David Andrew Harris, Ryan C McCormick, Jeffrey E Cohen, Tao Jin, Wei Feng, Rebecca D Levit and 2 more

Abstract read
In one paragraph

Article in Heart, lung & circulation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact, top 96% 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

11 citing papers in PubMed, 1 citations in OpenAlex.

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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

12 authors.

Pavan AtluriDivision of Cardiovascular Surgery, Department of Surgery, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, United States.
Corinna M Panlilio
George P Liao
William Hiesinger
David Andrew Harris
Ryan C McCormick
Jeffrey E Cohen
Tao Jin
Wei Feng
Rebecca D Levit
Nianguo Dong
Y Joseph Woo

Funding

ANGIOGENIC TISSUE ENGINEERING TO LIMIT POST-INFARCTION VENTRICULAR REMODELINGR01HL089315 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI WOO, Y JOSEPH · 2008 to 2023
$6.4M
Angiogenesis and Cardiac Growth as Heart Failure TherapyK08HL072812 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI WOO, Y JOSEPH · 2004 to 2008
$662k
EPC mediated Neovascularization in Ischemic MyocardiumF32HL079769 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ATLURI, PAVAN · 2005 to 2006
$72k
NHLBI NIH HHS 1 F32 HL79769-01NHLBI NIH HHS F32 HL079769NHLBI NIH HHS HL072812NHLBI NIH HHS K08 HL072812NHLBI NIH HHS R01 HL089315
6 · The paper itself

Abstract

purposePost-myocardial infarction heart failure is a major health concern with limited therapy. Molecular revascularisation utilising granulocyte-macrophage colony stimulating factor (GMCSF) mediated endothelial progenitor cell (EPC) upregulation and stromal cell derived factor-1α (SDF) mediated myocardial EPC chemokinesis, may prevent myocardial loss and adverse remodelling. Vasculogenesis, viability, and haemodynamic improvements following therapy were investigated. PROCEDURES: Lewis rats (n=91) underwent LAD ligation and received either intramyocardial SDF and subcutaneous GMCSF or saline injections at the time of infarction. Molecular and haemodynamic assessments were performed at pre-determined time points following ligation.

findingsSDF/GMCSF therapy upregulated EPC density as shown by flow cytometry (0.12±0.02% vs. 0.06±0.01% circulating lymphocytes, p=0.005), 48hours following infarction. A marked increase in perfusion was evident eight weeks after therapy, utilising confocal angiography (5.02±1.7×10(-2)μm(3)blood/μm(3)myocardial tissue vs. 2.03±0.710(-2)μm(3)blood/μm(3)myocardial tissue, p=0.00004). Planimetric analysis demonstrated preservation of wall thickness (0.98±0.09mm vs. 0.67±0.06mm, p=0.003) and ventricular diameter (7.81±0.99mm vs. 9.41±1.1mm, p=0.03). Improved haemodynamic function was evidenced by echocardiography and PV analysis (ejection fraction: 56.4±18.1% vs. 25.3±15.6%, p=0.001; pre-load adjusted maximal power: 6.6±2.6mW/μl(2) vs. 2.7±1.4mW/μl(2), p=0.01).

conclusionNeovasculogenic therapy with GMCSF-mediated EPC upregulation and SDF-mediated EPC chemokinesis maybe an effective therapy for infarct modulation and preservation of myocardial function following acute myocardial infarction.

Indexed as

AnimalsApoptosisChemokine CXCL12EchocardiographyEndothelial CellsFlow CytometryGranulocyte-Macrophage Colony-Stimulating FactorHeartHeart VentriclesHematopoietic Stem CellsHemodynamicsMaleModels, AnimalMyocardial InfarctionMyocardiumNeovascularization, PhysiologicChemokine CXCL12Granulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID20719564
PMCPMC3235678
OpenAlexW947843062

What OpenQuestion holds

Textmetadata
LicenceTDM
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.