Key result
Mitochondrial dysfunction is a central mediator of diabetic cardiomyopathy, suggesting that therapeutic approaches targeting mitochondrial biology hold promise for managing heart failure in diabetes.
Mitochondrial dysfunction plays a central role in the pathogenesis of diabetic cardiomyopathy, presenting a potential therapeutic target for heart failure in diabetic patients.
Should not yet change practice in diabetic cardiomyopathy; hypothesis-generating for mitochondrial-targeted therapies and requires prospective trials.
SIGNIFICANCE: Diabetes is an important risk factor for the development of heart failure (HF). Given the increasing prevalence of diabetes in the population, strategies are needed to reduce the burden of HF in these patients. RECENT ADVANCES: Diabetes is associated with several pathologic findings in the heart including dysregulated metabolism, lipid accumulation, oxidative stress, and inflammation. Emerging evidence suggests that mitochondrial dysfunction may be a central mediator of these pathologic responses. The development of therapeutic approaches targeting mitochondrial biology holds promise for the management of HF in diabetic patients. CRITICAL ISSUES: Despite significant data implicating mitochondrial pathology in diabetic cardiomyopathy, the optimal pharmacologic approach to improve mitochondrial function remains undefined. FUTURE DIRECTIONS: Detailed mechanistic studies coupled with more robust clinical phenotyping will be necessary to develop novel approaches to improve cardiac function in diabetes. Moreover, understanding the interplay between diabetes and other cardiac stressors (hypertension, ischemia, and valvular disease) will be of the utmost importance for clinical translation of scientific discoveries made in this field.
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Joel D. Schilling (2015) conducted a review in Diabetic heart failure. Mitochondrial dysfunction is a central mediator of diabetic cardiomyopathy, suggesting that therapeutic approaches targeting mitochondrial biology hold promise for managing heart failure in diabetes.
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