Fischer Roland, Longo Filomena, Nielsen Peter, Engelhardt Rainer, Hider Robert C, Piga Antonio
Institut für Molekulare Zellbiologie, Universitätsklinikum Hamburg-Eppendorf, Germany.
Br J Haematol. 2003 Jun;121(6):938-48. doi: 10.1046/j.1365-2141.2003.04297.x.
In this non-randomized prospective study, liver and spleen iron concentrations were monitored annually over a 4-year period by non-invasive Superconducting Quantum Interference Device biomagnetometry in 54 beta-thalassaemia major patients (age, 7-22 years) receiving treatment with deferiprone (75 mg/kg/d). Median liver iron concentrations increased significantly from 1456 to 2029 and 2449 microg/g(liver) at baseline, after 2.0 and 3.2 years respectively. Another group of 51 thalassaemic patients (aged 4-34 years) who received desferrioxamine s.c. for 1.9 years increased their liver iron concentration from 1076 to 1260 microg/g(liver). Taking into account the increase of the daily iron input from transfusions of 3.6 mg/d, caused by weight gain in 67% of the patients treated with deferiprone, a larger total body iron elimination rate was achieved after 2 years than at baseline. A negative ferritin change was observed in 51% of the patients. In 15 non-splenectomized patients, liver iron significantly increased from 1260 to 1937 microg/g(liver) (P < 0.01), but serum ferritin remained stable at 2100 microg/l, as did the spleen iron concentration at 1200 microg/g(spleen). A two-compartment model may predict an average chelation efficacy for desferrioxamine and deferiprone, with a saturation effect of the latter, for a certain chelation and transfusion regimen by a single liver iron quantification.
在这项非随机前瞻性研究中,采用无创超导量子干涉装置生物磁测量法,对54例接受去铁酮(75mg/kg/d)治疗的重型β地中海贫血患者(年龄7 - 22岁)进行了为期4年的年度肝脏和脾脏铁浓度监测。肝脏铁浓度中位数在基线时为1456μg/g(肝脏),分别在2.0年和3.2年后显著增加至2029μg/g(肝脏)和2449μg/g(肝脏)。另一组51例接受皮下注射去铁胺1.9年的地中海贫血患者(年龄4 - 34岁),其肝脏铁浓度从1076μg/g(肝脏)增加至1260μg/g(肝脏)。考虑到67%接受去铁酮治疗的患者因体重增加导致输血每日铁输入量增加3.6mg/d,2年后总体铁清除率高于基线水平。51%的患者观察到铁蛋白呈负向变化。在15例未行脾切除术的患者中,肝脏铁从1260μg/g(肝脏)显著增加至1937μg/g(肝脏)(P<0.01),但血清铁蛋白稳定在2100μg/L,脾脏铁浓度稳定在1200μg/g(脾脏)。两室模型可通过单次肝脏铁定量预测去铁胺和去铁酮对于特定螯合和输血方案的平均螯合效果,以及后者的饱和效应。