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Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population

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 repolarizat...

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Autores principales: Russo, Vincenzo, Papa, Andrea Antonio, Rago, Anna, D'Ambrosio, Paola, Cimmino, Giovanni, Palladino, Alberto, Politano, Luisa, Nigro, Gerardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore SRL 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343740/
https://www.ncbi.nlm.nih.gov/pubmed/28344440
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author Russo, Vincenzo
Papa, Andrea Antonio
Rago, Anna
D'Ambrosio, Paola
Cimmino, Giovanni
Palladino, Alberto
Politano, Luisa
Nigro, Gerardo
author_facet Russo, Vincenzo
Papa, Andrea Antonio
Rago, Anna
D'Ambrosio, Paola
Cimmino, Giovanni
Palladino, Alberto
Politano, Luisa
Nigro, Gerardo
author_sort Russo, Vincenzo
collection PubMed
description 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.
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spelling pubmed-53437402017-03-24 Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population Russo, Vincenzo Papa, Andrea Antonio Rago, Anna D'Ambrosio, Paola Cimmino, Giovanni Palladino, Alberto Politano, Luisa Nigro, Gerardo Acta Myol Original Articles 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. Pacini Editore SRL 2016-10 /pmc/articles/PMC5343740/ /pubmed/28344440 Text en The journal and the individual contributions contained in it are protected by the copyright of Gaetano Conte Academy, Naples, Italy http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License, which permits for noncommercial use, distribution, and reproduction in any digital medium, provided the original work is properly cited and is not altered in any way. For details, please refer to http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Articles
Russo, Vincenzo
Papa, Andrea Antonio
Rago, Anna
D'Ambrosio, Paola
Cimmino, Giovanni
Palladino, Alberto
Politano, Luisa
Nigro, Gerardo
Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title_full Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title_fullStr Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title_full_unstemmed Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title_short Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
title_sort increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343740/
https://www.ncbi.nlm.nih.gov/pubmed/28344440
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