Physiology and pathophysiology of iron in hemoglobin-associated diseases

被引:120
|
作者
Coates, Thomas D. [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Childrens Hosp Los Angeles, Childrens Ctr Canc & Blood Dis, Los Angeles, CA 90027 USA
关键词
Hemoglobinopathy; Thalassemia; Iron overload; Hemochromatosis; Sickle cell disease; Magnetic resonance imaging; Chelation; ROS; Iron toxicity; Transfusion; TRANSFERRIN-BOUND IRON; BETA-THALASSEMIA MAJOR; SICKLE-CELL-ANEMIA; TRANSFUSION-DEPENDENT THALASSEMIA; ATTENUATES OXIDATIVE STRESS; DIAMOND-BLACKFAN ANEMIA; SERUM HEPCIDIN LEVELS; LABILE PLASMA IRON; CHELATION-THERAPY; MYOCARDIAL IRON;
D O I
10.1016/j.freeradbiomed.2014.03.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Iron overload and iron toxicity, whether because of increased absorption or iron loading from repeated transfusions, can be major causes of morbidity and mortality in a number of chronic anemias. Significant advances have been made in our understanding of iron homeostasis over the past decade. At the same time, advances in magnetic resonance imaging have allowed clinicians to monitor and quantify iron concentrations noninvasively in specific organs. Furthermore, effective iron chelators are now available, including preparations that can be taken orally. This has resulted in substantial improvement in mortality and morbidity for patients with severe chronic iron overload. This paper reviews the key points of iron homeostasis and attempts to place clinical observations in patients with transfusional iron overload in context with the current understanding of iron homeostasis in humans. (C) 2014 Elsevier Inc. All rights reserved.
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页码:23 / 40
页数:18
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