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Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies

Despite recent advances in the management of patients with heart failure, morbidity and mortality rates remain high. Common causes of heart failure are ischaemic heart disease, uncontrolled hypertension and valvular disease. However, in up to 50 % of the cases its exact cause remains initially unkno...

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Detalles Bibliográficos
Autores principales: Hazebroek, M., Dennert, R., Heymans, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402574/
https://www.ncbi.nlm.nih.gov/pubmed/22618228
http://dx.doi.org/10.1007/s12471-012-0285-7
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author Hazebroek, M.
Dennert, R.
Heymans, S.
author_facet Hazebroek, M.
Dennert, R.
Heymans, S.
author_sort Hazebroek, M.
collection PubMed
description Despite recent advances in the management of patients with heart failure, morbidity and mortality rates remain high. Common causes of heart failure are ischaemic heart disease, uncontrolled hypertension and valvular disease. However, in up to 50 % of the cases its exact cause remains initially unknown; this condition is called idiopathic dilated cardiomyopathy (DCM). Improved diagnostic methods, most notably the advancements in molecular and immunohistological biopsy techniques and genetic research, have endorsed a new era in the diagnosis and classification of patients with idiopathic DCM. These insights have led to novel aetiology-based treatment strategies and improved outcome. The present article will briefly discuss all causes of DCM with a special focus on inflammatory- and virus-mediated forms of DCM.
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spelling pubmed-34025742012-08-03 Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies Hazebroek, M. Dennert, R. Heymans, S. Neth Heart J ICIN Despite recent advances in the management of patients with heart failure, morbidity and mortality rates remain high. Common causes of heart failure are ischaemic heart disease, uncontrolled hypertension and valvular disease. However, in up to 50 % of the cases its exact cause remains initially unknown; this condition is called idiopathic dilated cardiomyopathy (DCM). Improved diagnostic methods, most notably the advancements in molecular and immunohistological biopsy techniques and genetic research, have endorsed a new era in the diagnosis and classification of patients with idiopathic DCM. These insights have led to novel aetiology-based treatment strategies and improved outcome. The present article will briefly discuss all causes of DCM with a special focus on inflammatory- and virus-mediated forms of DCM. Bohn Stafleu van Loghum 2012-05-22 2012-08 /pmc/articles/PMC3402574/ /pubmed/22618228 http://dx.doi.org/10.1007/s12471-012-0285-7 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle ICIN
Hazebroek, M.
Dennert, R.
Heymans, S.
Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title_full Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title_fullStr Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title_full_unstemmed Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title_short Idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
title_sort idiopathic dilated cardiomyopathy: possible triggers and treatment strategies
topic ICIN
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402574/
https://www.ncbi.nlm.nih.gov/pubmed/22618228
http://dx.doi.org/10.1007/s12471-012-0285-7
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