Evidence map›Paper›PMID 33458574›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2020

Impaired myocardial strain in early stage of Duchenne muscular dystrophy: its relation with age and motor performance.

Lilia Oreto, Gian Luca Vita, Giuseppe Mandraffino, Scipione Carerj, Maria Pia Calabrò, Roberta Manganaro, Maurizio Cusmà-Piccione, Maria Chiara Todaro, Maria Sframeli, Maria Cinquegrani and 4 more

Open access · greenAbstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Global longitudinal strain detects subtle left ventricular systolic dysfunction in Duchenne muscular dystrophy patients and carriers.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2021
    Article
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

14 authors at 2 institutions in 1 country.

Lilia OretoMediterranean Pediatric Cardiologic Centre, S. Vincenzo Hospital, Taormina - "Bambin Gesù", Rome, Italy.
Gian Luca VitaNemo Sud Clinical Centre for Neuromuscular Disorders, Messina University Hospital, Messina, Italy.
Giuseppe MandraffinoInternal Medicine Unit, Department of Clinical and Experimental Medicine, University of Messina, Italy.
Scipione CarerjCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Maria Pia CalabròPediatric Unit, Department of Human Pathology in Adult and Developmental Age, University of Messina, Italy.
Roberta ManganaroCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Maurizio Cusmà-PiccioneCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Maria Chiara TodaroCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Maria SframeliNemo Sud Clinical Centre for Neuromuscular Disorders, Messina University Hospital, Messina, Italy.
Maria CinquegraniInternal Medicine Unit, Department of Clinical and Experimental Medicine, University of Messina, Italy.
Antonio ToscanoUnit of Neurology and Neuromuscular Disorders, Department of Clinical and Experimental Medicine, University of Messina, Italy.
Giuseppe VitaNemo Sud Clinical Centre for Neuromuscular Disorders, Messina University Hospital, Messina, Italy.
Sonia MessinaNemo Sud Clinical Centre for Neuromuscular Disorders, Messina University Hospital, Messina, Italy.
Concetta ZitoCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
University of Messina · ITAzienda Ospedaliera Ospedali Riuniti Papardo Piemonte · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is complicated by an early and progressive left ventricular (LV) dysfunction. Despite the reduction of ejection fraction (EF) usually manifests in the second decade, subtle alterations in LV mechanics can be detected earlier. Longitudinal and circumferential LV deformation, evaluated by speckle tracking echocardiography (STE), are considered sensitive markers of early dysfunction. We retrospectively examined clinical and echocardiographic data of 32 DMD children with preserved LV function. According to the median age, patients were then divided into younger and older than 9 years, and compared to 24 age-matched healthy subjects. Six-minute-walk test (6MWT), North Star Ambulatory Assessment (NSAA), and a comprehensive cardiac evaluation were performed. Although EF was within the normal range, DMD patients had significantly lower values than healthy controls, and the same occurred for the remaining conventional systolic and diastolic indices. Global longitudinal strain (GLS) was reduced in all patients (older and younger, both p < 0.001). Global circumferential strain (GCS) was reduced only in older patients (< 0.001). Both GLS and GCS worsened with age in DMD patients (GLS p = 0.005; GCS p = 0.024). GLS was significantly worse in the apical segments and in the postero-lateral wall. GCS in the antero-septal, anterior and antero-lateral segments was significantly reduced in older patients, with a prevalent involvement of the sole septal wall in the younger boys. 6MWT appeared to be correlated inversely to GLS and directly to EF. A longitudinal evaluation should be scheduled in DMD boys to assess the global cardiac performance over time and to evaluate the impact of therapies.

Indexed as

AdolescentAge FactorsChildChild, PreschoolEchocardiographyHumansMaleMotor ActivityMuscular Dystrophy, DuchenneRetrospective StudiesStroke VolumeVentricular Dysfunction, LeftWalk TestcardiomyopathyDuchenne muscular dystrophymotor performancespeckle tracking echocardiographystrain

Identifiers

PMID33458574
PMCPMC7783425
OpenAlexW3125620729

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.