| Literature DB >> 31109456 |
Hao Zhang1, Pavel Zhabyeyev1, Shaohua Wang2, Gavin Y Oudit3.
Abstract
Iron metabolism is a balancing act, and biological systems have evolved exquisite regulatory mechanisms to maintain iron homeostasis. Iron metabolism disorders are widespread health problems on a global scale and range from iron deficiency to iron-overload. Both types of iron disorders are linked to heart failure. Iron play a fundamental role in mitochondrial function and various enzyme functions and iron deficiency has a particular negative impact on mitochondria function. Given the high-energy demand of the heart, iron deficiency has a particularly negative impact on heart function and exacerbates heart failure. Iron-overload can result from excessive gut absorption of iron or frequent use of blood transfusions and is typically seen in patients with congenital anemias, sickle cell anemia and beta-thalassemia major, or in patients with primary hemochromatosis. This review provides an overview of normal iron metabolism, mechanisms underlying development of iron disorders in relation to heart failure, including iron-overload cardiomyopathy, and clinical perspective on the treatment options for iron metabolism disorders.Entities:
Keywords: Cardiomyopathy; Genetic regulation; Heart failure; Hemochromatosis; Hepcidin; Iron deficiency; Iron metabolism; Iron overload; Mitochondrial function
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Year: 2018 PMID: 31109456 DOI: 10.1016/j.bbadis.2018.08.030
Source DB: PubMed Journal: Biochim Biophys Acta Mol Basis Dis ISSN: 0925-4439 Impact factor: 5.187