Iron chelating agents in clinical practice

被引:97
作者
Faa, G
Crisponi, G
机构
[1] Univ Cagliari, Dipartimento Citomorfol, Sez Anat Patol, I-09124 Cagliari, Italy
[2] Univ Cagliari, Dipartimento Chim & Tecnol Inorgan & Met Organ, I-09124 Cagliari, Italy
关键词
iron-chelators; desferrioxamine; deferiprone; thalassemia;
D O I
10.1016/S0010-8545(99)00056-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The relevance of iron chelators in medicine has increased in recent years, Iron is essential for life but it is also potentially more toxic than other trace elements. This is due to the lack of effective means to protect human cells against iron overload and to the role of iron in the generation of free radicals. To protect patients from the consequences of iron toxicity, iron chelating agents have been introduced in clinical practice. Unfortunately, the ideal chelator for treating iron overload in humans has not been identified yet. The aim of this review is to report the experience with desferrioxamine therapy in patients affected by beta-thalassemia major according to: bioavailability; mechanism of interactions with hepatocellular iron: release of iron chelates and their excretion, impact of iron chelation on survival in thalassemia patients and side effects of prolonged therapy. Problems related to the development of non-toxic oral iron chelators are also discussed, with particular emphasis on the preliminary data on usefulness and safety of deferiprone (L1), recently evaluated in different clinical trials. Iron chelating therapy has been introduced, in recent years, ec en in the therapy of disorders not characterized by iron overload. Here the following new therapeutic indications are discussed: adult respiratory distress syndrome, myocardial ischemia, cancer and malaria. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:291 / 310
页数:20
相关论文
共 144 条
[1]   METAL-COMPLEX FORMATION OF A NEW SIDEROPHORE DESFERRITHIOCIN AND OF 3 RELATED LIGANDS [J].
ANDEREGG, G ;
RABER, M .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (17) :1194-1196
[2]   SUDDEN CARDIAC-TAMPONADE AFTER CHEMOTHERAPY FOR MARROW TRANSPLANTATION IN THALASSEMIA [J].
ANGELUCCI, E ;
MARIOTTI, E ;
LUCARELLI, G ;
BARONCIANI, D ;
CESARONI, P ;
DURAZZI, SMT ;
GALIMBERTI, M ;
GIARDINI, C ;
MURETTO, P ;
POLCHI, P ;
SGARBI, E .
LANCET, 1992, 339 (8788) :287-289
[3]   Limitations of magnetic resonance imaging in measurement of hepatic iron [J].
Angelucci, E ;
Giovagnoni, A ;
Valeri, G ;
Paci, E ;
Ripalti, M ;
Muretto, P ;
McLaren, C ;
Brittenham, GM ;
Lucarelli, G .
BLOOD, 1997, 90 (12) :4736-4742
[4]   Chemometric methods applied to an ICP-AES study of chemical element distributions in autopsy livers from subjects affected by Wilson and beta-thalassemia [J].
Aragoni, MC ;
Crisponi, G ;
Nurchi, VM ;
Silvagni, R ;
Sciot, R ;
Ambu, R ;
Costa, V ;
Faa, G .
JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY, 1995, 9 (04) :215-221
[5]  
BALDWIN SR, 1986, LANCET, V1, P11
[6]   THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
BALK, R ;
BONE, RC .
MEDICAL CLINICS OF NORTH AMERICA, 1983, 67 (03) :685-700
[7]   G1549, A NEW CYCLIC HYDROXAMIC ACID ANTIBIOTIC, ISOLATED FROM CULTURE BROTH OF PSEUDOMONAS-ALCALIGENES [J].
BARKER, WR ;
CALLAGHAN, C ;
HILL, L ;
NOBLE, D ;
ACRED, P ;
HARPER, PB ;
SOWA, MA ;
FLETTON, RA .
JOURNAL OF ANTIBIOTICS, 1979, 32 (11) :1096-1103
[8]   LONG-TERM CHELATION THERAPY IN THALASSEMIA MAJOR - EFFECT ON LIVER IRON CONCENTRATION, LIVER HISTOLOGY, AND CLINICAL PROGRESS [J].
BARRY, M ;
FLYNN, DM ;
LETSKY, EA ;
RISDON, RA .
BMJ-BRITISH MEDICAL JOURNAL, 1974, 2 (5909) :16-20
[9]  
Bel A, 1996, ACTA HAEMATOL-BASEL, V95, P63
[10]  
BERGERON RJ, 1993, BLOOD, V81, P2166