Targeting the hepcidin-ferroportin axis to develop new treatment strategies for anemia of chronic disease and anemia of inflammation

被引:141
作者
Sun, Chia Chi [1 ]
Vaja, Valentina [1 ,2 ]
Babitt, Jodie L. [1 ]
Lin, Herbert Y. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Program Membrane Biol,Div Nephrol, Ctr Syst Biol,Richard B Simches Res Ctr,Med Sch, 185 Cambridge St,CPZN-8216, Boston, MA 02114 USA
[2] Univ Milan, Fdn Ist Ricovero & Cura Carattere Sci Ca Granda, Milan, Italy
关键词
CHRONIC KIDNEY-DISEASE; RECOMBINANT-HUMAN-ERYTHROPOIETIN; IRON-DEFICIENCY ANEMIA; REGULATORY HORMONE HEPCIDIN; PLACEBO-CONTROLLED TRIAL; QUALITY-OF-LIFE; HEMODIALYSIS-PATIENTS; IN-VIVO; INTRAVENOUS IRON; HEREDITARY HEMOCHROMATOSIS;
D O I
10.1002/ajh.23110
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anemia of chronic disease (ACD) or anemia of inflammation is prevalent in patients with chronic infection, autoimmune disease, cancer, and chronic kidney disease. ACD is associated with poor prognosis and lower quality of life. Management of ACD using intravenous iron and erythropoiesis stimulating agents are ineffective for some patients and are not without adverse effects, driving the need for new alternative therapies. Recent advances in our understanding of the molecular mechanisms of iron regulation reveal that increased hepcidin, the iron regulatory hormone, is a key factor in the development of ACD. In this review, we will summarize the role of hepcidin in iron homeostasis, its contribution to the pathophysiology of ACD, and novel strategies that modulate hepcidin and its target ferroportin for the treatment of ACD. Am. J. Hematol. 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:392 / 400
页数:9
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