LPI-labile plasma iron in iron overload

被引:232
作者
Cabantchik, ZI [1 ]
Breuer, W
Zanninelli, G
Cianciulli, R
机构
[1] Hebrew Univ Jerusalem, Life Sci Program, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Inst Life Sci, Dept Biol Chem, IL-91904 Jerusalem, Israel
[3] Osped St Eugenio, Unita Day Hosp Talassemici, Rome, Italy
关键词
labile plasma iron; iron overload; thalassemia; hemosiderosis; transfusion; hemochromatosis; ascorbate; oxidative stress; fluorescence; high throughput assay;
D O I
10.1016/j.beha.2004.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Labile plasma iron (LPI) represents a component of non-transferrin-bound iron (NTBI) that is both redox-active and chelatable, capable of permeating into organs and inducing tissue iron overload. It appears in various types of hemosiderosis (transfusional and non-transfusional) and in other iron-overload conditions. Sustained levels of LPI could over time compromise organ (e.g. heart) function and patient survival. With the advent of methods for measuring LPI in the clinical setting, it has become possible to assess the implications of LPI in the management of iron overload based on regimens of iron chelation. As LPI is detected primarily in patients with transfusional iron overload and other forms of hemosiderosis, we review here regimens of iron chelation with deferrioxamine and deferiprone (separately or combined) in terms of their efficacy in minimizing daily exposure to LPI in thalassemia major and thalassemia intermedia patients.
引用
收藏
页码:277 / 287
页数:11
相关论文
共 35 条
[31]   Serum chelatable redox-active iron is an independent predictor of mortality after myocardial infarction in individuals with diabetes [J].
Sulieman, M ;
Asleh, R ;
Cabantchik, ZI ;
Breuer, W ;
Aronson, D ;
Suleiman, A ;
Miller-Loian, R ;
Hammerman, H ;
Levy, AP .
DIABETES CARE, 2004, 27 (11) :2730-2732
[32]   Pathophysiology of thalassaemia [J].
Weatherall, DJ .
BAILLIERES CLINICAL HAEMATOLOGY, 1998, 11 (01) :127-146
[33]  
Westwood M, 2003, HAEMATOLOGICA, V88, P481
[34]  
Winder A, 2003, BLOOD, V102, p916A
[35]   Myocardial iron loading in transfusion-dependent thalassemia and sickle cell disease [J].
Wood, JC ;
Tyszka, JM ;
Carson, S ;
Nelson, MD ;
Coates, TD .
BLOOD, 2004, 103 (05) :1934-1936