2010, Number S1
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Rev Mex Med Transfus 2010; 3 (S1)
Therapy of iron chelation
López SN
Language: Spanish
References: 24
Page: 80-86
PDF size: 224.59 Kb.
ABSTRACT
The iron (Fe) is a necessary metal for enzymatic systems function. Most of iron is contained into hemoglobin and it’s function is gaseous exchange between tissue and lung; in other enzymatic systems iron takes part in different oxide-reduction mechanism. During normal physiology, quantity of iron absorbed (2 mg/d) is lost by sloughing of intestinal mucosa and skin, in a close equilibrium. This quantity is insufficient for maintain the erythropoiesis, that use the iron from the physiologic hemolysis, 18 mg/day; this iron has no other active mechanism for the excretion. In patients transfusion-dependent there is an iron excess approximately 3.46 mg/g of hemoglobin transfused or 250 mg/unit. The iron from the hemolysis is binding to ferritin and hemosyderin, when this proteins are full there is iron overload and gradually accumulates in several tissues: in the liver at first, but when it stands in high levels it’s deposited in any organs such as heart, glands, ganglion, skin, etc., and more danger, could stay free as non binding transferring iron (NBTI), the most toxic iron form to the human. The use of different substances that binding the iron and help for excretion it, are the best option for limit iron toxicity. Actually we have different substances for this objective: deferoxamine, deferiprone and deferasirox.
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