Evidence map›Paper›PMID 26784932›Full record

ArticlePloS one2016

Widespread Myocardial Delivery of Heart-Derived Stem Cells by Nonocclusive Triple-Vessel Intracoronary Infusion in Porcine Ischemic Cardiomyopathy: Superior Attenuation of Adverse Remodeling Documented by Magnetic Resonance Imaging and Histology.

Eleni Tseliou, Hideaki Kanazawa, James Dawkins, Romain Gallet, Michelle Kreke, Rachel Smith, Ryan Middleton, Jackelyn Valle, Linda Marbán, Saibal Kar and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04703751 (Evaluation of the CIRCULATE Catheter for Transcoronary Administration of Pharmacologic and Cell-based Agents), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.8field-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.

NCT04703751 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Evaluation of the CIRCULATE Catheter for Transcoronary Administration of Pharmacologic and Cell-based Agents

TypeinterventionalSponsorJohn Paul II Hospital, KrakowRan2022 to 2022Enrolled10ConditionsDilated CardiomyopathyArmsTranscoronary delivery of a pharmacological agent (nitroglycerin) and cell based agent (Cardiocell) using the CIRCULATE Catheter
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 33 citations in OpenAlex.

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  14. Is Cardioprotection Dead?Circulation · 2017
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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 at 2 institutions in 2 countries.

Eleni TseliouCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Hideaki KanazawaKeio University School of Medicine, Tokyo, Japan.
James DawkinsCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Romain GalletCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Michelle KrekeCapricor Inc., Los Angeles, CA, United States of America.
Rachel SmithCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Ryan MiddletonCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Jackelyn ValleCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Linda MarbánCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Saibal KarCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Rajendra MakkarCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Eduardo MarbánCedars-Sinai Heart Institute, Los Angeles, CA, United States of America.
Capricor Therapeutics (United States) · USKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-vessel, intracoronary infusion of stem cells under stop-flow conditions has proven safe but achieves only limited myocardial coverage. Continuous flow intracoronary delivery to one or more coronary vessels may achieve broader coverage for treating cardiomyopathy, but has not been investigated. Using nonocclusive coronary guiding catheters, we infused allogeneic cardiosphere-derived cells (CDCs) either in a single vessel or sequentially in all three coronary arteries in porcine ischemic cardiomyopathy and used magnetic resonance imaging (MRI) to assess structural and physiological outcomes. Vehicle-infused animals served as controls. Single-vessel stop-flow and continuous-flow intracoronary infusion revealed equivalent effects on scar size and function. Sequential infusion into each of the three major coronary vessels under stop-flow or continuous-flow conditions revealed equal efficacy, but less elevation of necrotic biomarkers with continuous-flow delivery. In addition, multi-vessel delivery resulted in enhanced global and regional tissue function compared to a triple-vessel placebo-treated group. The functional benefits after global cell infusion were accompanied histologically by minimal inflammatory cellular infiltration, attenuated regional fibrosis and enhanced vessel density in the heart. Sequential multi-vessel non-occlusive delivery of CDCs is safe and provides enhanced preservation of left ventricular function and structure. The current findings provide preclinical validation of the delivery method currently undergoing clinical testing in the Dilated cardiomYopathy iNtervention With Allogeneic MyocardIally-regenerative Cells (DYNAMIC) trial of CDCs in heart failure patients.

Indexed as

Stem Cell TransplantationAnimalsCardiomyopathy, HypertrophicCell- and Tissue-Based TherapyDisease Models, AnimalImmunohistochemistryMagnetic Resonance ImagingMyoblasts, CardiacMyocardial InfarctionMyocardial IschemiaPhenotypeStem CellsStroke VolumeSwineVentricular Remodeling

Identifiers

PMID26784932
PMCPMC4718597
OpenAlexW2337936917

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.