Iron overload cardiomyopathy: Using the latest evidence to inform future applications.

Abstract

Iron overload can be the result of either dysregulated iron metabolism in the case of hereditary hemochromatosis or repeated blood transfusions in the case of secondary hemochromatosis (e.g. in β-thalassemia and sickle cell anemia patients). Under iron overload conditions, transferrin (Tf) saturation leads to an increase in non-Tf bound iron which can result in the generation of reactive oxygen species (ROS). These excess ROS can damage cellular components, resulting in the dysfunction of vital organs including iron overload cardiomyopathy (IOC). Multiple studies have demonstrated that L-type and T-type calcium channels are the main routes for iron uptake in the heart, and that calcium channel blockers, given either individually or in combination with standard iron chelators, confer cardioprotective effects under iron overload conditions. Treatment with antioxidants may also provide therapeutic benefits. Interestingly, recent studies have suggested that mitochondrial dynamics and regulated cell death (RCD) pathways are potential targets for pharmacological interventions against iron-induced cardiomyocyte injury. In this review, the potential therapeutic roles of iron chelators, antioxidants, iron uptake/metabolism modulators, mitochondrial dynamics modulators, and inhibitors of RCD pathways in IOC are summarized and discussed.

• Authors: Sirinart Kumfu, Siriporn C Chattipakorn, Nipon Chattipakorn
• Journal: Experimental biology and medicine (Maywood, N.J.) (Exp Biol Med (Maywood)) Vol. 247 Issue 7 Pg. 574-583 (04 2022) ISSN: 1535-3699 [Electronic] England
• PMID: 35130741 (Publication Type: Journal Article, Review)

Chemical References

• Antioxidants
• Iron Chelating Agents
• Reactive Oxygen Species
• Iron

Topics

• Antioxidants (therapeutic use)
• Cardiomyopathies (drug therapy)
• Hemochromatosis (complications, drug therapy, metabolism)
• Humans
• Iron (metabolism)
• Iron Chelating Agents (metabolism, pharmacology, therapeutic use)
• Iron Overload (complications, drug therapy)
• Myocytes, Cardiac (metabolism)
• Reactive Oxygen Species (metabolism)