Evidence map›Paper›PMID 31239508›Full record

ArticleScientific reports2019

A comprehensive, multiscale framework for evaluation of arrhythmias arising from cell therapy in the whole post-myocardial infarcted heart.

Joseph K Yu, William Franceschi, Qinwen Huang, Farhad Pashakhanloo, Patrick M Boyle, Natalia A Trayanova

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

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  19. Editorial: Modeling of cardiovascular systems.Frontiers in physiology · 2022
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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

6 authors at 1 institution in 1 country.

Joseph K YuInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA.
William FranceschiInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA.
Qinwen HuangInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA.
Farhad PashakhanlooInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA.
Patrick M BoyleInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA.ORCID http://orcid.org/0000-0001-9048-1239
Natalia A TrayanovaInstitute for Computational Medicine, Johns Hopkins University, 3400 N Charles St, 216 Hackerman Hall, Baltimore, Maryland, 21218, USA. ntrayanova@jhu.edu.
Johns Hopkins University · US

Funding

Virtual Electrophysiology LaboratoryDP1HL123271 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TRAYANOVA, NATALIA A. · 2013 to 2017
$4.0M
Infarct-related Ventricular Tachycardia Mechanisms: From Micro to ClinicalR01HL142496 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TRAYANOVA, NATALIA A. · 2019 to 2022
$3.1M
Exploration of Arrhythmogenic Triggers and Substrates in Heart FailureR01HL126802 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI EFIMOV, IGOR R, GORELIK, JULIA · 2016 to 2019
$2.8M
Resynchronizing the Failing Heart: Insights from a Multiscale Cardiac ModelR01HL103428 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TRAYANOVA, NATALIA A. · 2011 to 2014
$2.3M
NHLBI NIH HHS DP1 HL123271NHLBI NIH HHS R01 HL103428NHLBI NIH HHS R01 HL126802NHLBI NIH HHS R01 HL142496
6 · The paper itself

Abstract

Direct remuscularization approaches to cell-based heart repair seek to restore ventricular contractility following myocardial infarction (MI) by introducing new cardiomyocytes (CMs) to replace lost or injured ones. However, despite promising improvements in cardiac function, high incidences of ventricular arrhythmias have been observed in animal models of MI injected with pluripotent stem cell-derived cardiomyocytes (PSC-CMs). The mechanisms of arrhythmogenesis remain unclear. Here, we present a comprehensive framework for computational modeling of direct remuscularization approaches to cell therapy. Our multiscale 3D whole-heart modeling framework integrates realistic representations of cell delivery and transdifferentiation therapy modalities as well as representation of spatial distributions of engrafted cells, enabling simulation of clinical therapy and the prediction of emergent electrophysiological behavior and arrhythmogenensis. We employ this framework to explore how varying parameters of cell delivery and transdifferentiation could result in three mechanisms of arrhythmogenesis: focal ectopy, heart block, and reentry.

Indexed as

Models, TheoreticalAnimalsArrhythmias, CardiacCell- and Tissue-Based TherapyCell DifferentiationMyocardial InfarctionMyocytes, CardiacPluripotent Stem CellsRabbitsRegenerationStem Cell Transplantation

Identifiers

PMID31239508
PMCPMC6592890
OpenAlexW2955574854

What OpenQuestion holds

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LicenceCC BY
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.