Key result
This review highlights the dysregulation of mitochondrial representation and bioenergetics in specific skeletal muscle disorders caused by mutations disrupting muscle cell integrity.
Why the study?
The specific roles of mitochondria and energetic metabolism in skeletal muscle under muscle-wasting conditions in cardiomyopathies have not been investigated in detail and remain poorly characterized.
This review highlights the poorly characterized role of mitochondrial dysregulation in skeletal muscle wasting associated with genetic neuromuscular disorders and cardiomyopathies.
Mitochondrial roles in neuromuscular cardiomyopathies warrant integrated assessment; extends mechanistic insights but leaves open targeted therapies.
Mitochondrial dysfunction is considered the major contributor to skeletal muscle wasting in different conditions. Genetically determined neuromuscular disorders occur as a result of mutations in the structural proteins of striated muscle cells and therefore are often combined with cardiac phenotype, which most often manifests as a cardiomyopathy. The specific roles played by mitochondria and mitochondrial energetic metabolism in skeletal muscle under muscle-wasting conditions in cardiomyopathies have not yet been investigated in detail, and this aspect of genetic muscle diseases remains poorly characterized. This review will highlight dysregulation of mitochondrial representation and bioenergetics in specific skeletal muscle disorders caused by mutations that disrupt the structural and functional integrity of muscle cells.
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Ignatieva et al. (2021) conducted a review in Genetic neuromuscular disorders with cardiac phenotype. Mitochondrial dysfunction was evaluated. This review highlights the dysregulation of mitochondrial representation and bioenergetics in specific skeletal muscle disorders caused by mutations disrupting muscle cell integrity.
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