Cardiomyopathies

Journal article

The cardiomyopathies are a heterogeneous collection of heart muscle disorders with diverse genetic and non-genetic aetiologies. The advent of molecular genetics and next-generation sequencing has transformed understanding of the mechanisms of disease underlying many forms of cardiomyopathy, and unlocked the prospect of personalized medicine based on knowledge of an individual's genetic variants. Current management of patients with inherited cardiomyopathies is beginning to integrate knowledge of individual genomic profiles with advances in cardiovascular imaging. This has enhanced surveillance potential for high-risk individuals and begun to facilitate diagnosis, appropriate risk stratification and prognostication. This review provides an introduction to the cardiomyopathies, focusing on hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic cardiomyopathy and left ventricular non-compaction, giving an overview of their aetiological complexity, diagnosis and contemporary clinical management.

Authors: Chan, K; Harper, A; Ashrafian, H; Yavari, A

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Elsevier
• Journal: Medicine
• Volume: 46
• Issue: 10
• Pages: 606-617
• Publication date: 2018-09-03
• Acceptance date: 2018-07-20
• DOI: 10.1016/j.mpmed.2018.07.014
• EISSN: 1365-4357
• ISSN: 1357-3039
• Keywords: sudden cardiac death; restrictive cardiomyopathy; genetic; cardiomyopathy; hypertrophic cardiomyopathy; left ventricular non-compaction; Arrhythmogenic right ventricular dysplasia; dilated cardiomyopathy