Moving beyond simple answers to complex disorders in sarcomeric cardiomyopathies: the role of integrated systems.
Andrea E DeranekMatthew M KlassJil C TardiffPublished in: Pflugers Archiv : European journal of physiology (2019)
The classic clinical definition of hypertrophic cardiomyopathy (HCM) as originally described by Teare is deceptively simple, "left ventricular hypertrophy in the absence of any identifiable cause." Longitudinal studies, however, including a seminal study performed by Frank and Braunwald in 1968, clearly described the disorder much as we know it today, a complex, progressive, and highly variable cardiomyopathy affecting ~ 1/500 individuals worldwide. Subsequent genetic linkage studies in the early 1990s identified mutations in virtually all of the protein components of the cardiac sarcomere as the primary molecular cause of HCM. In addition, a substantial proportion of inherited dilated cardiomyopathy (DCM) has also been linked to sarcomeric protein mutations. Despite our deep understanding of the overall function of the sarcomere as the primary driver of cardiac contractility, the ability to use genotype in patient management remains elusive. A persistent challenge in the field from both the biophysical and clinical standpoints is how to rigorously link high-resolution protein dynamics and mechanics to the long-term cardiovascular remodeling process that characterizes these complex disorders. In this review, we will explore the depth of the problem from both the standpoint of a multi-subunit, highly conserved and dynamic "machine" to the resultant clinical and structural human phenotype with an emphasis on new, integrative approaches that can be widely applied to identify both novel disease mechanisms and new therapeutic targets for these primary biophysical disorders of the cardiac sarcomere.
Keyphrases
- hypertrophic cardiomyopathy
- left ventricular
- heart failure
- acute myocardial infarction
- cardiac resynchronization therapy
- high resolution
- mitral valve
- left atrial
- aortic stenosis
- protein protein
- multiple sclerosis
- endothelial cells
- gene expression
- transcription factor
- small molecule
- coronary artery disease
- mass spectrometry
- dna methylation
- case control
- atrial fibrillation
- aortic valve
- hepatitis c virus
- acute coronary syndrome
- induced pluripotent stem cells