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先天性贫血患儿长期输血中的非转铁蛋白结合铁

Non-transferrin-bound iron in long-term transfusion in children with congenital anemias.

作者信息

Wang W C, Ahmed N, Hanna M

出版信息

J Pediatr. 1986 Apr;108(4):552-7. doi: 10.1016/s0022-3476(86)80832-0.

Abstract

Non-transferrin-bound iron (NTBI), a potentially toxic compound, is increased in the serum of patients with iron overload and fully saturated transferrin. We found markedly elevated NTBI levels in 16 children (including nine with sickle cell disease and five with beta-thalassemia) with iron overload secondary to prolonged transfusion therapy. During iron chelation with subcutaneous desferrioxamine infusion, NTBI levels decreased to normal, but became elevated within 2 to 4 hours after discontinuation of desferrioxamine. NTBI causes hepatic and cardiac toxicity in experimental systems, but our patients lacked sufficient organ dysfunction for this association to be made. The use of continuous 24-hour chelation to maintain NTBI at low levels may prevent progressive iron toxicity in patients who first received chelation therapy at an older age or who already have evidence of cardiac damage.

摘要

非转铁蛋白结合铁(NTBI)是一种潜在的有毒化合物,在铁过载且转铁蛋白完全饱和的患者血清中含量会升高。我们发现,16名因长期输血治疗导致铁过载的儿童(包括9名镰状细胞病患儿和5名β地中海贫血患儿)的NTBI水平显著升高。在皮下输注去铁胺进行铁螯合治疗期间,NTBI水平降至正常,但在停止去铁胺治疗后2至4小时内又会升高。在实验系统中,NTBI会导致肝脏和心脏毒性,但我们的患者没有足够的器官功能障碍来证实这种关联。对于首次在较大年龄接受螯合治疗或已有心脏损伤证据的患者,采用24小时持续螯合以使NTBI维持在低水平,可能会预防渐进性铁毒性。

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