Evidence map›Paper›PMID 23757309›Full record

ArticleCirculation2013

Intracoronary delivery of autologous cardiac stem cells improves cardiac function in a porcine model of chronic ischemic cardiomyopathy.

Roberto Bolli, Xian-Liang Tang, Santosh K Sanganalmath, Ornella Rimoldi, Federico Mosna, Ahmed Abdel-Latif, Hani Jneid, Marcello Rota, Annarosa Leri, Jan Kajstura

Open access · bronzeAbstract read
In one paragraph

Article in Circulation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
14.8field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 235 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. To Repair a Broken Heart: Stem Cells in Ischemic Heart Disease.Current issues in molecular biology · 2024
    Review
  5. Review
  6. Cell Therapy in the Treatment of Coronary Heart Disease.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Effects of Heme Oxygenase-1 on c-Kit-Positive Cardiac Cells.International journal of molecular sciences · 2021
    Article

67 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Roberto BolliDivision of Cardiovascular Medicine and Institute of Molecular Cardiology, University of Louisville, Louisville, KY 40202, USA. rbolli@louisville.edu
Xian-Liang Tang
Santosh K Sanganalmath
Ornella Rimoldi
Federico Mosna
Ahmed Abdel-Latif
Hani Jneid
Marcello Rota
Annarosa Leri
Jan Kajstura
University of Louisville · USSan Raffaele University of Rome · ITLifeArc · GBInstitute of Molecular Bioimaging and Physiology · IT

Funding

Tumor Necrosis Factor Modulation of CPCsP01HL078825 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2005 to 2021
$37.6M
The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI REN, HONGMEI · 2012 to 2017
$13.7M
OXYGEN RADICALS AND CARDIAC ADAPTATIONS TO ISCHEMIAR37HL055757 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2000 to 2009
$4.9M
Stem Cells and Myocardial Aging in DogsP01AG043353 · NIA · UNIVERSITY OF ALBUQUERQUE · PI BUCHHOLZ, BRUCE A · 2013 to 2015
$4.5M
Mechanisms of CardioprotectionR01HL070897 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2003 to 2007
$2.8M
Late Preconditioning in HypercholesterolemiaR01HL074351 · NHLBI · UNIVERSITY OF LOUISVILLE · PI ROKOSH, GREGG, TANG, XIAN-LIANG · 2003 to 2012
$2.3M
MOLECULAR BASIS OF PRECONDITIONINGR01HL068088 · NHLBI · UNIVERSITY OF LOUISVILLE · PI GUO, YIRU · 2001 to 2005
$2.3M
Redefining Human Myocardial BiologyR01HL105532 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO, BUCHHOLZ, BRUCE A · 2011 to 2014
$2.2M
Hematopoietic Stem Cell Therapy for Myocardial RegenerationR01HL076794 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2004 to 2007
$1.9M
Telomeric Shortening, p53 and miR-34a Condition Senescence of Cardiac ProgenitorsR01AG037490 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA · 2010 to 2014
$1.7M
Cardiomyogenesis in the Adult HeartR01HL114346 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA, ROTA, MARCELLO · 2012 to 2015
$1.7M
Cardiac Stem Cells and AngiomyogenesisR01HL111183 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA · 2012 to 2015
$1.7M
Medical Research Council G0300395NHLBI NIH HHS HL-55757NHLBI NIH HHS HL-70897NHLBI NIH HHS HL-74351NHLBI NIH HHS HL-76794NHLBI NIH HHS HL-78825NHLBI NIH HHS HL-91202NHLBI NIH HHS P01 HL078825NHLBI NIH HHS R01 HL055757NHLBI NIH HHS R01 HL068088NHLBI NIH HHS R01 HL070897NHLBI NIH HHS R01 HL074351NHLBI NIH HHS R01 HL076794NHLBI NIH HHS R01 HL091202NHLBI NIH HHS R01 HL111183NHLBI NIH HHS R01 HL114346NHLBI NIH HHS R01-HL-68088NHLBI NIH HHS R37 HL055757NIA NIH HHS P01 AG043353NIA NIH HHS R01 AG037490NIGMS NIH HHS P20 GM103527
6 · The paper itself

Abstract

backgroundRelevant preclinical models are necessary for further mechanistic and translational studies of c-kit+ cardiac stem cells (CSCs). The present study was undertaken to determine whether intracoronary CSCs are beneficial in a porcine model of chronic ischemic cardiomyopathy. METHODS AND

resultsPigs underwent a 90-minute coronary occlusion followed by reperfusion. Three months later, autologous CSCs (n=11) or vehicle (n=10) were infused into the infarct-related artery. At this time, all indices of left ventricular (LV) function were similar in control and CSC-treated pigs, indicating that the damage inflicted by the infarct in the 2 groups was similar; 1 month later, however, CSC-treated pigs exhibited significantly greater LV ejection fraction (echocardiography) (51.7±2.0% versus 42.9±2.3%, P<0.01), systolic thickening fraction in the infarcted LV wall, and maximum LV dP/dt, as well as lower LV end-diastolic pressure. Confocal microscopy showed clusters of small α-sarcomeric actin-positive cells expressing Ki67 in the scar of treated pigs, consistent with cardiac regeneration. The origin of these cycling myocytes from the injected cells was confirmed in 4 pigs that received enhanced green fluorescent protein -labeled CSCs, which were positive for the cardiac markers troponin I, troponin T, myosin heavy chain, and connexin-43. Some engrafted CSCs also formed vascular structures and expressed α-smooth muscle actin.

conclusionsIntracoronary infusion of autologous CSCs improves regional and global LV function and promotes cardiac and vascular regeneration in pigs with old myocardial infarction (scar). The results mimic those recently reported in humans (Stem Cell Infusion in Patients with Ischemic CardiOmyopathy [SCIPIO] trial) and establish this porcine model of ischemic cardiomyopathy as a useful and clinically relevant model for studying CSCs.

Indexed as

Disease Models, AnimalAnimalsCardiomyopathiesCells, CulturedCoronary VesselsInfusions, Intra-ArterialMaleMyocardial IschemiaMyocytes, CardiacStem Cell TransplantationSwineTransplantation, Autologousangiogenesis inducersheart failuremuscle developmentmyocardial infarctionstem cells

Identifiers

PMID23757309
PMCPMC3807652
OpenAlexW1976468926

What OpenQuestion holds

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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.