More pieces to the iron chelation puzzle.
More pieces to the iron chelation puzzle.
复制标题
铁螯合拼图的更多部分。
DOI:
10.1016/j.trsl.2010.06.006
复制
发表时间:
2010
期刊:
影响因子:
--
通讯作者:
Waalen,Jill
中科院分区:
文献类型:
--
作者:
Waalen,Jill
Regular blood transfusions are life-saving treatment for patients with severe anemias, including those with beta thalassemia, sickle cell disease, myelodysplastic syndromes, and other conditions. But, the treatment is a double-edged sword–each unit of transfused blood contains 200 mg of iron and because the body has no mechanism to excrete excess iron, chronic iron overload often results, causing damage to the liver, heart, endocrine organs, and other tissues. Iron chelation therapy, thus, has played a vital role in the management of these patients since the introduction of the parenterally administered chelator deferoxamine (DFO) more than 40 years ago.In this issue, Evans, et al. report on in vitro kinetic studies of the interaction of DFO with deferiprone (DFP), in removing non-transferrin bound iron from plasma of thalassemic patients. DFP is an oral agent first used in humans in the late 1980s and DFO/DFP combination therapy has been under clinical study for most of the two decades since. However, controversy still exists over how the agents interact in removing iron and how they can be administered together most effectively.