Hepcidin and iron metabolism: From laboratory to clinical implications

被引:45
|
作者
Franchini, Massimo [1 ]
Montagnana, Martina [2 ]
Lippi, Giuseppe [3 ]
机构
[1] Azienda Osped Univ Parma, Serv Immunoematol & Med Trasfus, Dipartimento Patol & Med Lab, Parma, Italy
[2] Azienda Osped Univ Integrata Verona, Sez Chim, Dipartimento Sci Morfol Biomed, Verona, Italy
[3] Azienda Osped Univ Parma, UO Diagnost Ematochim, Dipartimento Patol & Med Lab, Parma, Italy
关键词
Hepcidin; Iron; Anemia; Hemochromatosis; ANTIMICROBIAL PEPTIDE; EXPRESSION; ANEMIA; FERROPORTIN; ABSORPTION; HYPOXIA; URINARY; GENE; HEMOCHROMATOSIS; QUANTIFICATION;
D O I
10.1016/j.cca.2010.07.003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Hepcidin is a liver-synthesized hormone that inhibits the cellular efflux of iron by binding to ferroportin and its subsequent degradation. The main role of hepcidin is regulation of ferroportin expression and cell membrane function. Recent studies implicate hepcidin in a variety of iron disorders in addition to its primary role in the regulation of systemic iron homeostasis. Hepcidin excess has a key pathologic role in anemia of inflammation, chronic kidney disease, and iron-refractory iron deficiency anemia, while hepcidin deficiency is responsible for most cases of familial hemochromatosis and iron-loading anemia. The most important advances on the role of hepcidin in normal and abnormal iron metabolism and the main clinical and diagnostic implications are summarized in this review. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1565 / 1569
页数:5
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