Evidence map›Paper›PMID 24315764›Full record

ArticleJournal of the American Society of Echocardiography : official publication of the American Society of Echocardiography2014

Echocardiographic evaluation of the effects of stem cell therapy on perfusion and function in ischemic cardiomyopathy.

Yoichi Inaba, Brian P Davidson, Sajeevani Kim, Ya Ni Liu, William Packwood, J Todd Belcik, Aris Xie, Jonathan R Lindner

Open access · greenAbstract readEvaluation StudyValidation Study
In one paragraph

Article in Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. A novel method for quantitative myocardial contrast echocardiography in mice.American journal of physiology. Heart and circulatory physiology · 2018
    Article
  6. Ischemic memory imaging in nonhuman primates with echocardiographic molecular imaging of selectin expression.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2014
    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

8 authors at 1 institution in 1 country.

Yoichi InabaKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Brian P DavidsonKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Sajeevani KimKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Ya Ni LiuKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
William PackwoodKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
J Todd BelcikKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Aris XieKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Jonathan R LindnerKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon. Electronic address: linderj@ohsu.edu.
Oregon Health & Science University · US

Funding

Targeted CEU Imaging of Atherosclerosis and AngiogenesisR01HL078610 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2022
$6.8M
Biomarkers of Inflammation and Vaso-occlusion in Sickle Cell DiseaseR01HL111969 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI FIELD, JOSHUA JEFFREY, LINDEN, JOEL M. · 2012 to 2016
$4.0M
Training in Translational Science and Cardiovascular MedicineT32HL094294 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ALKAYED, NABIL J · 2009 to 2018
$3.5M
Ultrasound Assessment of Microvascular Function in Insulin Resistant PrimatesR01DK063508 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2002 to 2011
$2.7M
Contrast-enhanced Ultrasound Assessment of AngiogenesisR01HL074443 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2007
$1.5M
Molecular Imaging of Ischemic Memory with Ultrasound - Transition to HumansRC1HL100659 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LINDNER, JONATHAN R · 2009 to 2010
$979k
NHLBI NIH HHS R01 HL074443NHLBI NIH HHS R01 HL078610NHLBI NIH HHS R01-HL-078610NHLBI NIH HHS R01 HL111969NHLBI NIH HHS R01-HL111969NHLBI NIH HHS RC1 HL100659NHLBI NIH HHS RC1-HL-100659NHLBI NIH HHS T32 HL094294NHLBI NIH HHS T32-HL094294NIDDK NIH HHS R01 DK063508
6 · The paper itself

Abstract

backgroundSmall animal models of ischemic left ventricular (LV) dysfunction are important for the preclinical optimization of stem cell therapy. The aim of this study was to test the hypothesis that temporal changes in LV function and regional perfusion after cell therapy can be assessed in mice using echocardiographic imaging.

methodsWild-type mice (n = 25) were studied 7 and 28 days after permanent ligation of the left anterior descending coronary artery. Animals were randomized to receive closed-chest ultrasound-guided intramyocardial delivery of saline (n = 13) or 5 × 10(5) multipotential adult progenitor cells (MAPCs; n = 12) on day 7. LV end-diastolic and end-systolic volumes, LV ejection fraction, and stroke volume were measured using high-frequency echocardiography. Multiplanar assessments of perfusion and defect area size were made using myocardial contrast echocardiography.

resultsBetween days 7 and 28, MAPC-treated animals had 40% to 50% reductions in defect size (P < .001) and 20% to 30% increases in total perfusion (P < .01). Perfusion did not change in nontreated controls. Both LV end-diastolic and end-systolic volumes increased between days 7 and 28 in both groups, but LV end-systolic volume increased to a lesser degree in MAPC-treated compared with control mice (+4.2 ± 7.9 vs +19.2 ± 22.0 μL, P < .05). LV ejection fraction increased in the MAPC-treated mice and decreased in control mice (+3.0 ± 4.3% vs -5.6 ± 5.9%, P < .01). There was a significant linear relation between the change in LV ejection fraction and the change in either defect area size or total perfusion.

conclusionsHigh-frequency echocardiography and myocardial contrast echocardiography in murine models of ischemic LV dysfunction can be used to assess the response to stem cell therapy and to characterize the relationship among spatial flow, ventricular function, and ventricular remodeling.

Indexed as

EchocardiographyStem Cell TransplantationAnimalsDisease Models, AnimalMiceMice, NudeMultipotent Stem CellsMyocardial IschemiaMyocardial Perfusion ImagingRandom AllocationRatsVentricular Dysfunction, LeftVentricular RemodelingContrast echocardiographyEchocardiographyLADLeft anterior descending coronary arteryLeft ventricularLeft ventricular ejection fractionLeft ventricular end-diastolic volumeLeft ventricular end-systolic volumeLVLVEDVLVEFLVESVMAPCMCEMicrobubblesMultipotential adult progenitor cellMyocardial contrast echocardiographyStem cells

Identifiers

PMID24315764
PMCPMC3946830
OpenAlexW1984532873

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.