Cargando…

Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes

Lamin A/C gene mutations can be associated with cardiac diseases, usually referred to as ‘cardiolaminopathies’ characterized by arrhythmic disorders and/or left ventricular or biventricular dysfunction up to an overt picture of heart failure. The phenotypic cardiac manifestations of laminopathies ar...

Descripción completa

Detalles Bibliográficos
Autores principales: Boriani, Giuseppe, Biagini, Elena, Ziacchi, Matteo, Malavasi, Vincenzo Livio, Vitolo, Marco, Talarico, Marisa, Mauro, Erminio, Gorlato, Giulia, Lattanzi, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244733/
https://www.ncbi.nlm.nih.gov/pubmed/30130999
http://dx.doi.org/10.1080/19491034.2018.1506680
_version_ 1783372106777493504
author Boriani, Giuseppe
Biagini, Elena
Ziacchi, Matteo
Malavasi, Vincenzo Livio
Vitolo, Marco
Talarico, Marisa
Mauro, Erminio
Gorlato, Giulia
Lattanzi, Giovanna
author_facet Boriani, Giuseppe
Biagini, Elena
Ziacchi, Matteo
Malavasi, Vincenzo Livio
Vitolo, Marco
Talarico, Marisa
Mauro, Erminio
Gorlato, Giulia
Lattanzi, Giovanna
author_sort Boriani, Giuseppe
collection PubMed
description Lamin A/C gene mutations can be associated with cardiac diseases, usually referred to as ‘cardiolaminopathies’ characterized by arrhythmic disorders and/or left ventricular or biventricular dysfunction up to an overt picture of heart failure. The phenotypic cardiac manifestations of laminopathies are frequently mixed in complex clinical patterns and specifically may include bradyarrhythmias (sinus node disease or atrioventricular blocks), atrial arrhythmias (atrial fibrillation, atrial flutter, atrial standstill), ventricular tachyarrhythmias and heart failure of variable degrees of severity. Family history, physical examination, laboratory findings (specifically serum creatine phosphokinase values) and ECG findings are often important ‘red flags’ in diagnosing a ‘cardiolaminopathy’. Sudden arrhythmic death, thromboembolic events or stroke and severe heart failure requiring heart transplantation are the most dramatic complications of the evolution of cardiolaminopathies and appropriate risk stratification is clinically needed combined with clinical follow-up. Treatment with cardiac electrical implantable devices is indicated in case of bradyarrhythmias (implant of a device with pacemaker functions), risk of life-threatening ventricular tachyarrhythmias (implant of an ICD) or in case of heart failure with wide QRS interval (implant of a device for cardiac resynchronization). New technologies introduced in the last 5 years can help physicians to reduce device-related complications, thanks to the extension of device longevity and availability of leadless pacemakers or defibrillators, to be implanted in appropriately selected patients. An improved knowledge of the complex pathophysiological pathways involved in cardiolaminopathies and in the determinants of their progression to more severe forms will help to improve clinical management and to better target pharmacological and non-pharmacological treatments.
format Online
Article
Text
id pubmed-6244733
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-62447332018-11-26 Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes Boriani, Giuseppe Biagini, Elena Ziacchi, Matteo Malavasi, Vincenzo Livio Vitolo, Marco Talarico, Marisa Mauro, Erminio Gorlato, Giulia Lattanzi, Giovanna Nucleus Special issue on Laminopathies Lamin A/C gene mutations can be associated with cardiac diseases, usually referred to as ‘cardiolaminopathies’ characterized by arrhythmic disorders and/or left ventricular or biventricular dysfunction up to an overt picture of heart failure. The phenotypic cardiac manifestations of laminopathies are frequently mixed in complex clinical patterns and specifically may include bradyarrhythmias (sinus node disease or atrioventricular blocks), atrial arrhythmias (atrial fibrillation, atrial flutter, atrial standstill), ventricular tachyarrhythmias and heart failure of variable degrees of severity. Family history, physical examination, laboratory findings (specifically serum creatine phosphokinase values) and ECG findings are often important ‘red flags’ in diagnosing a ‘cardiolaminopathy’. Sudden arrhythmic death, thromboembolic events or stroke and severe heart failure requiring heart transplantation are the most dramatic complications of the evolution of cardiolaminopathies and appropriate risk stratification is clinically needed combined with clinical follow-up. Treatment with cardiac electrical implantable devices is indicated in case of bradyarrhythmias (implant of a device with pacemaker functions), risk of life-threatening ventricular tachyarrhythmias (implant of an ICD) or in case of heart failure with wide QRS interval (implant of a device for cardiac resynchronization). New technologies introduced in the last 5 years can help physicians to reduce device-related complications, thanks to the extension of device longevity and availability of leadless pacemakers or defibrillators, to be implanted in appropriately selected patients. An improved knowledge of the complex pathophysiological pathways involved in cardiolaminopathies and in the determinants of their progression to more severe forms will help to improve clinical management and to better target pharmacological and non-pharmacological treatments. Taylor & Francis 2018-10-18 /pmc/articles/PMC6244733/ /pubmed/30130999 http://dx.doi.org/10.1080/19491034.2018.1506680 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special issue on Laminopathies
Boriani, Giuseppe
Biagini, Elena
Ziacchi, Matteo
Malavasi, Vincenzo Livio
Vitolo, Marco
Talarico, Marisa
Mauro, Erminio
Gorlato, Giulia
Lattanzi, Giovanna
Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title_full Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title_fullStr Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title_full_unstemmed Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title_short Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
title_sort cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes
topic Special issue on Laminopathies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244733/
https://www.ncbi.nlm.nih.gov/pubmed/30130999
http://dx.doi.org/10.1080/19491034.2018.1506680
work_keys_str_mv AT borianigiuseppe cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT biaginielena cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT ziacchimatteo cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT malavasivincenzolivio cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT vitolomarco cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT talaricomarisa cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT mauroerminio cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT gorlatogiulia cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes
AT lattanzigiovanna cardiolaminopathiesfrombenchtobedsidechallengesinclinicaldecisionmakingwithfocusonarrhythmiarelatedoutcomes