Evidence map›Paper›PMID 25814625›Full record

ArticleJournal of the American Heart Association2015

Myocardial fibrosis burden predicts left ventricular ejection fraction and is associated with age and steroid treatment duration in duchenne muscular dystrophy.

Animesh Tandon, Chet R Villa, Kan N Hor, John L Jefferies, Zhiqian Gao, Jeffrey A Towbin, Brenda L Wong, Wojciech Mazur, Robert J Fleck, Joshua J Sticka and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 1 pooled it
10.4field-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

92 citing papers in PubMed, 1 synthesis or guideline pooled it, 189 citations in OpenAlex.

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  14. Late Gadolinium Enhancement and Electrocardiographic Associations in Hypertrophic Cardiomyopathy.Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc · 2025
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Animesh TandonHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Chet R VillaHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Kan N HorThe Heart Center, Nationwide Children's Hospital, Columbus, OH (K.N.H.).
John L JefferiesHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Zhiqian GaoHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Jeffrey A TowbinHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Brenda L WongDivision of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (B.L.W.).
Wojciech MazurThe Heart and Vascular Center at the Christ Hospital, Cincinnati, OH (W.M.).
Robert J FleckThe Department of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (R.J.F.).
Joshua J StickaHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
D Woodrow BensonHerma Heart Center, Children's Hospital of Wisconsin, Milwaukee, WI (W.B.).
Michael D TaylorHeart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH (A.T., C.R.V., J.L.J., Z.G., J.A.T., J.J.S., M.D.T.).
Cincinnati Children's Hospital Medical Center · USChildren's Hospital of Wisconsin · USChrist Hospital · USNationwide Children's Hospital · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
NCATS NIH HHS UL1 TR000077NCATS NIH HHS UL1 TR001425NCRR NIH HHS 5UL1RR026314NCRR NIH HHS UL1 RR026314
6 · The paper itself

Abstract

backgroundPatients with Duchenne muscular dystrophy exhibit progressive cardiac and skeletal muscle dysfunction. Based on prior data, cardiac dysfunction in Duchenne muscular dystrophy patients may be influenced by myocardial fibrosis and steroid therapy. We examined the longitudinal relationship of myocardial fibrosis and ventricular dysfunction using cardiac magnetic resonance in a large Duchenne muscular dystrophy cohort. METHODS AND

resultsWe reviewed 465 serial cardiac magnetic resonance studies (98 Duchenne muscular dystrophy patients with ≥4 cardiac magnetic resonance studies) for left ventricular ejection fraction (LVEF) and presence of late gadolinium enhancement (LGE), a marker for myocardial fibrosis. LVEF was modeled by examining LGE status, myocardial fibrosis burden (as assessed by the number of LGE-positive left ventricular segments), patient age, and steroid treatment duration. An age-only model demonstrated that LVEF declined 0.58 ± 0.10% per year. In patients with both LGE-negative and LGE-positive studies (n=51), LVEF did not decline significantly over time if LGE was absent but declined 2.2 ± 0.31% per year when LGE was present. Univariate modeling showed significant associations between LVEF and steroid treatment duration, presence of LGE, and number of LGE-positive left ventricular segments; multivariate modeling showed that LVEF declined by 0.93 ± 0.09% for each LGE-positive left ventricular segment, whereas age and steroid treatment duration were not significant. The number of LGE-positive left ventricular segments increased with age, and longer steroid treatment duration was associated with lower age-related increases.

conclusionProgressive myocardial fibrosis, as detected by LGE, was strongly correlated with the LVEF decline in Duchenne muscular dystrophy patients. Longer steroid treatment duration was associated with a lower age-related increase in myocardial fibrosis burden.

Indexed as

AdolescentAdultAge FactorsChildDisease ProgressionFibrosisGlucocorticoidsHeartHumansMagnetic Resonance ImagingMaleMuscular Dystrophy, DuchenneMyocardiumPrednisonePregnenedionesRetrospective StudiesdeflazacortGlucocorticoidsPrednisonePregnenedionescardiomyopathymagnetic resonance imagingmorbidity

Identifiers

PMID25814625
PMCPMC4579941
OpenAlexW2024852223

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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.