Evidence map›Paper›PMID 39268580›Full record

ArticleDisease models & mechanisms2024

Functional cardiac consequences of β-adrenergic stress-induced injury in a model of Duchenne muscular dystrophy.

Conner C Earl, Areli J Javier, Alyssa M Richards, Larry W Markham, Craig J Goergen, Steven S Welc

Abstract read
In one paragraph

Article in Disease models & mechanisms, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Conner C EarlWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.ORCID 0000-0002-7916-3165
Areli J JavierMusculoskeletal Health Sciences Program, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-9056-9887
Alyssa M RichardsWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.
Larry W MarkhamDivision of Pediatric Cardiology, Riley Children's Hospital at Indiana University Health, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-2804-4641
Craig J GoergenWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.ORCID 0000-0001-8883-7953
Steven S WelcDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-2353-0325

Funding

Comprehensive Training Program in Musculoskeletal ResearchT32AR065971 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ALEXANDER G ROBLING · 2015 to 2026
$4.4M
Indiana Medical Scientist/Engineer Training ProgramT32GM148382 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI Benjamin Gaston, Emily K Sims · 2023 to 2026
$3.9M
Paracrine actions of fibroblasts promote pathologic cardiac myocyte remodeling in Duchenne muscular dystrophyR01HL158647 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI WELC, STEVEN S · 2021 to 2025
$2.6M
Spatiotemporal and Deep Learning Analysis of Cardiac Imaging for Predictive Risk Stratification in Duchenne Muscular DystrophyF30HL162452 · NHLBI · PURDUE UNIVERSITY · PI EARL, CONNER · 2022 to 2025
$220k
Indiana UniversityIndiana University-Purdue University IndianapolisIndiana University School of Medicine and Purdue University College of Engineering in Medicine Pilot Project InitiativeNHLBI NIH HHS F30 HL162452NHLBI NIH HHS F30HL162452NHLBI NIH HHS R01 HL158647NIAMS NIH HHS T32 AR065971NIAMS NIH HHS T32AR065971Purdue UniversityRiley Children's Foundation
6 · The paper itself

Abstract

Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD); however, in the mdx mouse model of DMD, the cardiac phenotype differs from that seen in DMD-associated cardiomyopathy. Although some have used pharmacologic stress to stimulate injury and enhance cardiac pathology in the mdx model, many methods lead to high mortality with variable cardiac outcomes, and do not recapitulate the structural and functional cardiac changes seen in human disease. Here, we describe a simple and effective method to enhance the cardiac phenotype model in mdx mice using advanced 2D and 4D high-frequency ultrasound to monitor cardiac dysfunction progression in vivo. mdx and wild-type mice received daily low-dose (2 mg/kg/day) isoproterenol injections for 10 days. Histopathological assessment showed that isoproterenol treatment increased myocyte injury, elevated serum cardiac troponin I levels and enhanced fibrosis in mdx mice. Ultrasound revealed reduced ventricular function, decreased wall thickness, increased volumes and diminished cardiac reserve in mdx compared to wild-type mice. Our findings highlight the utility of challenging mdx mice with low-dose isoproterenol as a valuable model for exploring therapies targeting DMD-associated cardiac pathologies.

Indexed as

Disease Models, AnimalFibrosisIsoproterenolMice, Inbred mdxMuscular Dystrophy, DuchenneAdrenergic beta-AgonistsAnimalsHeartMaleMiceMice, Inbred C57BLMyocardiumMyocytes, CardiacReceptors, Adrenergic, betaStress, PhysiologicalTroponin IAdrenergic beta-AgonistsIsoproterenolReceptors, Adrenergic, betaTroponin I4DUSCardiac strainDuchenne muscular dystrophyIsoproterenolmdxMouse model

Identifiers

PMID39268580
PMCPMC11488649

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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.