Evidence map›Paper›PMID 28344440›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2016

Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population.

Vincenzo Russo, Andrea Antonio Papa, Anna Rago, Paola D'Ambrosio, Giovanni Cimmino, Alberto Palladino, Luisa Politano, Gerardo Nigro

Abstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: a short term follow-up.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2018
    Article
  5. Myotonic dystrophy type 1 and pulmonary embolism: successful thrombus resolution with dabigatran etexilate therapy.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2018
    Article
  6. 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

8 authors.

Vincenzo RussoCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Andrea Antonio PapaCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Anna RagoCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Paola D'AmbrosioCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Giovanni CimminoCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Alberto PalladinoCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Luisa PolitanoCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.
Gerardo NigroCardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples and Monaldi Hospital, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden cardiac death in myotonic dystrophy type I (DM1) patients can be attributed to atrioventricular blocks as far as to the development of life-threatening arrhythmias which occur even in hearts with normal left ventricular systolic and diastolic function. Heterogeneity of ventricular repolarization is considered to provide an electrophysiological substrate for malignant arrhythmias. QTc dispersion (QTc-D), JTc dispersion (JTc-D) and transmural dispersion of repolarization (TDR) could reflect the physiological variability of regional and transmural ventricular repolarization. Aim of the present study was to investigate the heterogeneity of ventricular repolarization in patients with DM1 and preserved diastolic and systolic cardiac function. The study enrolled 50 DM1 patients (mean age 44 ± 5 years; M:F: 29:21) with preserved systolic and diastolic function of left ventricle among 247 DM1 patients followed at Cardiomyology and Medical Genetics of Second University of Naples, and 50 sexand age-matched healthy controls. The electrocardiographic parameters investigated were the following: Heart Rate, QRS duration, maximum and minimum QT and JT intervals, QTc- D, JTc-D and TDR. Compared to the controls, the DM1 group presented increased values of QTc-D (86.7 ± 40.1 vs 52.3 ± 11.9 ms; p = 0.03), JTc-D (78.6 ± 31.3 vs 61.3 ± 10.2 ms; p = 0.001) and TDR (101.6 ± 18.06 vs 90.1 ± 14.3 ms; p = 0.004) suggesting a significant increase in regional and transmural heterogeneity of the ventricular repolarization in these patients, despite a preserved systolic and diastolic cardiac function.

Indexed as

AdultArrhythmias, CardiacCase-Control StudiesEchocardiographyElectrocardiographyFemaleHeart VentriclesHumansMaleMiddle AgedMyotonic DystrophyVentricular Dysfunction, LeftarrhythmiasJTc dispersionmyotonic dystrophyQTc dispersionrepolarizationsudden cardiac death

Identifiers

PMID28344440
PMCPMC5343740

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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.