Iron overload cardiomyopathies: New insights into an old disease
- 1 February 1994
- journal article
- review article
- Published by Springer Nature in Cardiovascular Drugs and Therapy
- Vol. 8 (1) , 101-110
- https://doi.org/10.1007/bf00877096
Abstract
Iron overload cardiomyopathy is an old disease that has evolved from a rare undiagnosable and untreatable condition to a now much more common, diagnosable, and potentially treatable condition. Pathologically it is due to a direct free iron effect on the myocytes, and not due to interstitial infiltration. This also implies that the disease process is reversible if the tissue iron concentration can be controlled. The advent of magnetic resonance imaging and future genetic identification can identify the population at risk. Chelation therapy, including newer forms of oral chelators, likely will be more commonly available to benefit an ever increasing number and spectrum of the population. Further active research will be needed to improve our pathophysiological understanding and clinical treatment of this increasingly common condition.Keywords
This publication has 64 references indexed in Scilit:
- Prolonged survival in patients with beta-thalassemia major treated with deferoxamineThe Journal of Pediatrics, 1991
- Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood DonorsNew England Journal of Medicine, 1988
- Survival and Causes of Death in Cirrhotic and in Noncirrhotic Patients with Primary HemochromatosisNew England Journal of Medicine, 1985
- Prevention of Cardiac Disease by Subcutaneous Deferoxamine in Patients with Thalassemia MajorNew England Journal of Medicine, 1985
- The Declining Specificity of Exercise Radionuclide VentriculographyNew England Journal of Medicine, 1983
- Magnetic-Susceptibility Measurement of Human Iron StoresNew England Journal of Medicine, 1982
- The left ventricular end-systolic pressure-dimension relation in patients with thalassemia major. A new noninvasive method for assessing contractile state.Circulation, 1982
- Preclinical abnormal segmental cardiac manifestations of thalassemia major in children on transfusion-chelation therapy: Echographic alterations of left ventricular posterior wall contraction and relaxation patternsAmerican Heart Journal, 1982
- Clinical Consequences of Acquired Transfusional Iron Overload in AdultsNew England Journal of Medicine, 1981
- Detection of Early Cardiac Dysfunction in Patients with Severe Beta-Thalassemia and Chronic Iron OverloadNew England Journal of Medicine, 1979