Evidence map›Paper›PMID 34905152›Full record

ArticleThe international journal of cardiovascular imaging2022

Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy.

Nicolas Lanot, Marie Vincenti, Hamouda Abassi, Charlene Bredy, Audrey Agullo, Lucie Gamon, Thibault Mura, Kathleen Lavastre, Gregoire De La Villeon, Catherine Barrea and 7 more

Registry-linked trialOpen access · greenAbstract readControlled Clinical Trial
PubMed Publisher
In one paragraph

Article in The international journal of cardiovascular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02418338 (Evaluation of Myocardial Function by Two Dimensional Speckle Tracking Echocardiography in Children With Duchenne Muscular Dystrophy Versus Healthy Children), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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.

NCT02418338 nacompletednot on this map

Evaluation of Myocardial Function by Two Dimensional Speckle Tracking Echocardiography in Children With Duchenne Muscular Dystrophy Versus Healthy Children: a Comparative Transversal Multicenter Study

TypeinterventionalSponsorUniversity Hospital, MontpellierRan2014 to 2017Enrolled99ConditionsDuchenne Muscular DystrophyArmsspeckle tracking (2D strain) echocardiography
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

17 authors at 5 institutions in 2 countries.

Nicolas LanotPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-2712-0304
Marie VincentiPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-8201-5024
Hamouda AbassiPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-1876-5701
Charlene BredyPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.
Audrey AgulloPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0001-5979-7921
Lucie GamonEpidemiology and Clinical Research Department, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-0322-3384
Thibault MuraEpidemiology and Clinical Research Department, CHU Nimes, Nimes, France.ORCID http://orcid.org/0000-0001-6420-1336
Kathleen LavastrePaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.
Gregoire De La VilleonPaediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-3495-0173
Catherine BarreaPaediatric and Congenital Cardiology Department, Cliniques Universitaires Saint-Luc, UCL University, Brussels, Belgium.ORCID http://orcid.org/0000-0001-5008-0764
Pierre MeyerPhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0001-5710-7376
François RivierPhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-3896-8792
Albano C MeliPhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-1727-3027
Jeremy FauconnierPhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.
Olivier CazorlaPhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-0775-203X
Alain Lacampagne *PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-0264-1787
Pascal Amedro *Department of Paediatric and Adult Congenital Cardiology, M3C National Reference Centre, Bordeaux University Hospital, Haut Lévêque Hospital, Avenue de Magellan, 33604, Pessac Cedex, France. pascal.amedro@chu-bordeaux.fr.ORCID http://orcid.org/0000-0003-3649-0294
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nîmes · FRCliniques Universitaires Saint-Luc · BEUniversité de Bordeaux · FR

Funding

Centre Hospitalier Régional Universitaire de Montpellier PHRC-MERRI UF 9458French Muscular Dystrophy Association AFM 20225
6 · The paper itself

Abstract

Prognosis of Duchenne muscular dystrophy (DMD) is related to cardiac dysfunction. Two dimensional-speckle tracking echocardiography (2D-STE) has recently emerged as a non-invasive functional biomarker for early detection of DMD-related cardiomyopathy. This study aimed to determine, in DMD children, the existence of left ventricle (LV) dyssynchrony using 2D-STE analysis. This prospective controlled study enrolled 25 boys with DMD (mean age 11.0 ± 3.5 years) with normal LV ejection fraction and 50 age-matched controls. Three measures were performed to assess LV mechanical dyssynchrony: the opposing-wall delays (longitudinal and radial analyses), the modified Yu index, and the time-to-peak delays of each segment. Feasibility and reproducibility of 2D-STE dyssynchrony were evaluated. All three mechanical dyssynchrony criteria were significantly higher in the DMD group than in healthy subjects: (1) opposing-wall delays in basal inferoseptal to basal anterolateral segments (61.4 ± 45.3 ms vs. 18.3 ± 50.4 ms, P < 0.001, respectively) and in mid inferoseptal to mid anterolateral segments (58.6 ± 35.3 ms vs. 42.4 ± 36.4 ms, P < 0.05, respectively), (2) modified Yu index (33.3 ± 10.1 ms vs. 28.5 ± 8.1 ms, P < 0.05, respectively), and (3) most of time-to-peak values, especially in basal and mid anterolateral segments. Feasibility was excellent and reliability was moderate to excellent, with ICC values ranging from 0.49 to 0.97. Detection of LV mechanical dyssynchrony using 2D-STE analysis is an easily and reproducible method in paediatric DMD. The existence of an early LV mechanical dyssynchrony visualized using 2D-STE analysis in children with DMD before the onset of cardiomyopathy represents a perspective for future paediatric drug trials in the DMD-related cardiomyopathy prevention.Clinical Trial Registration Clinicaltrials.gov NCT02418338. Post-hoc study, registered on April 16, 2015.

Indexed as

Muscular Dystrophy, DuchenneVentricular Dysfunction, LeftAdolescentChildEchocardiographyHeart VentriclesHumansMalePredictive Value of TestsProspective StudiesReproducibility of ResultsCardiac dyssynchronyDMDHeart failurePaediatricsSpeckle tracking

Identifiers

PMID34905152
OpenAlexW4225823743

What OpenQuestion holds

Textmetadata
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.