The effect of emerging molecular and genetic therapies on cardiopulmonary disease in Duchenne muscular dystrophy.
Douglas A McKimTimothy P CripeLinda H CripePublished in: Pediatric pulmonology (2020)
Gene therapy is an attractive approach being intensively studied to prevent muscle deterioration in patients with Duchenne muscular dystrophy. While clinical trials are only in early stages, initial reports are promising for its effects on ambulation. Cardiopulmonary failure, however, is the most common cause of mortality in Duchenne muscular dystrophy (DMD) patients, and little is known regarding the prospects for gene therapy on alleviating DMD-associated cardiomyopathy and respiratory failure. Here we review current knowledge regarding effects of gene therapy on DMD cardiomyopathy and discuss respiratory endpoints that should be considered as outcome measures in future clinical trials.
Keyphrases
- duchenne muscular dystrophy
- gene therapy
- clinical trial
- respiratory failure
- end stage renal disease
- heart failure
- muscular dystrophy
- ejection fraction
- healthcare
- current status
- newly diagnosed
- chronic kidney disease
- extracorporeal membrane oxygenation
- prognostic factors
- mechanical ventilation
- peritoneal dialysis
- risk factors
- phase ii
- cardiovascular events
- coronary artery disease
- double blind
- respiratory tract