Copyright: ©Author(s) 2026.
World J Diabetes. Jul 15, 2026; 17(7): 120448
Published online Jul 15, 2026. doi: 10.4239/wjd.120448
Published online Jul 15, 2026. doi: 10.4239/wjd.120448
Figure 1 Graphic abstract.
Mitochondrial quality control and iron metabolism form a synergistic crosstalk in diabetic cardiomyopathy (DCM). Impaired mito chondrial 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.
- Citation: Tang YT, Wu Q, Chen YP, Xia L, Yang MH, Wei MY, Pang Q, Yang YN, Liu JB, Liu JL, Ni Q, Gong YB. Regulation of ferroptosis and mitochondrial homeostasis disruption in diabetic cardiomyopathy: Therapeutic potential of traditional Chinese medicine. World J Diabetes 2026; 17(7): 120448
- URL: https://www.wjgnet.com/1948-9358/full/v17/i7/120448.htm
- DOI: https://dx.doi.org/10.4239/wjd.120448