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Cardiomyopathies in China: A 2018–2019 state-of-the-art review

Cardiomyopathies are diseases of the cardiac muscle and are often characterized by ventricular dilation, hypertrophy, and cardiac arrhythmia. Patients with cardiomyopathies often experience sudden death and cardiac failure and require cardiac transplantation during the course of disease progression....

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Detalles Bibliográficos
Autores principales: Hua, Tian-Rui, Zhang, Shu-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Medical Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729112/
https://www.ncbi.nlm.nih.gov/pubmed/33336168
http://dx.doi.org/10.1016/j.cdtm.2020.05.006
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author Hua, Tian-Rui
Zhang, Shu-Yang
author_facet Hua, Tian-Rui
Zhang, Shu-Yang
author_sort Hua, Tian-Rui
collection PubMed
description Cardiomyopathies are diseases of the cardiac muscle and are often characterized by ventricular dilation, hypertrophy, and cardiac arrhythmia. Patients with cardiomyopathies often experience sudden death and cardiac failure and require cardiac transplantation during the course of disease progression. Early diagnosis, differential diagnosis, and genetic consultation depend on imaging techniques, genetic testing, and new emerging diagnostic tools such as serum biomarkers. The molecular genetics of cardiomyopathies has been widely studied recently. The discovery of mechanisms underlying heterogeneity and overlapping of the phenotypes of cardiomyopathies has revealed the existence of disease modifiers, and this has led to the emergence of novel disease-modifying therapy. This 2018–2019 state-of-the-art review outlines the pathogenesis, diagnosis, and treatment of cardiomyopathies in China.
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spelling pubmed-77291122020-12-16 Cardiomyopathies in China: A 2018–2019 state-of-the-art review Hua, Tian-Rui Zhang, Shu-Yang Chronic Dis Transl Med Review Cardiomyopathies are diseases of the cardiac muscle and are often characterized by ventricular dilation, hypertrophy, and cardiac arrhythmia. Patients with cardiomyopathies often experience sudden death and cardiac failure and require cardiac transplantation during the course of disease progression. Early diagnosis, differential diagnosis, and genetic consultation depend on imaging techniques, genetic testing, and new emerging diagnostic tools such as serum biomarkers. The molecular genetics of cardiomyopathies has been widely studied recently. The discovery of mechanisms underlying heterogeneity and overlapping of the phenotypes of cardiomyopathies has revealed the existence of disease modifiers, and this has led to the emergence of novel disease-modifying therapy. This 2018–2019 state-of-the-art review outlines the pathogenesis, diagnosis, and treatment of cardiomyopathies in China. Chinese Medical Association 2020-07-05 /pmc/articles/PMC7729112/ /pubmed/33336168 http://dx.doi.org/10.1016/j.cdtm.2020.05.006 Text en © 2020 Chinese Medical Association. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Hua, Tian-Rui
Zhang, Shu-Yang
Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title_full Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title_fullStr Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title_full_unstemmed Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title_short Cardiomyopathies in China: A 2018–2019 state-of-the-art review
title_sort cardiomyopathies in china: a 2018–2019 state-of-the-art review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729112/
https://www.ncbi.nlm.nih.gov/pubmed/33336168
http://dx.doi.org/10.1016/j.cdtm.2020.05.006
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