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Copyright: ©Author(s) 2026.
World J Diabetes. Jul 15, 2026; 17(7): 120448
Published online Jul 15, 2026. doi: 10.4239/wjd.120448
Figure 1
Figure 1 Graphic abstract. Mitochondrial quality control and iron metabolism form a synergistic crosstalk in diabetic cardiomyopathy (DCM). Impaired mitochondrial dynamics, biogenesis, and mitophagy, together with Fe²+ overload, oxidative stress, and lipid metabolism imbalance, contribute to ferroptosis, mitochondrial injury, and DCM progression. Current therapeutic strategies include sodium-glucose co-transporter-2 inhibitors, glucagon-like peptide-1 receptor agonists, iron chelators, mitochondrial protectants, and multi-target traditional Chinese medicine. Created with BioRender. DCM: Diabetic cardiomyopathy; SGLT2i: Sodium-glucose co-transporter-2 inhibitors; GLP-1RA: Glucagon-like peptide-1 receptor agonist; ROS: Reactive oxygen species.


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