Table of Contents Author Guidelines Submit a Manuscript
Biochemistry Research International
Volume 2012 (2012), Article ID 796926, 10 pages
Review Article

Cardiomyopathy Classification: Ongoing Debate in the Genomics Era

1Genomics Research Centre, Griffith Health Institute, Griffith University, Parklands Drive, Southport, QLD 4222, Australia
2Department of Cardiology, Gold Coast Hospital, Southport Campus, Nerang Street, Southport, QLD 4218, Australia

Received 8 March 2012; Revised 14 May 2012; Accepted 31 May 2012

Academic Editor: Aldrin V. Gomes

Copyright © 2012 Charles McCartan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases both primarily of the cardiac muscle and systemic diseases leading to adverse effects on the heart muscle size, shape, and function. Traditionally cardiomyopathies were defined according to phenotypical appearance. Now, as our understanding of the pathophysiology of the different entities classified under each of the different phenotypes improves and our knowledge of the molecular and genetic basis for these entities progresses, the traditional classifications seem oversimplistic and do not reflect current understanding of this myriad of diseases and disease processes. Although our knowledge of the exact basis of many of the disease processes of cardiomyopathies is still in its infancy, it is important to have a classification system that has the ability to incorporate the coming tide of molecular and genetic information. This paper discusses how the traditional classification of cardiomyopathies based on morphology has evolved due to rapid advances in our understanding of the genetic and molecular basis for many of these clinical entities.