Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease

被引:471
作者
Weinstein, DA
Roy, CN
Fleming, MD
Loda, MF
Wolfsdorf, JI
Andrews, NC
机构
[1] Harvard Univ, Sch Med, Childrens Hosp, Boston, MA USA
[2] Brigham & Womens Hosp, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Childrens Hosp, Howard Hughes Med Inst, Boston, MA USA
关键词
D O I
10.1182/blood-2002-04-1260
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The anemia of chronic disease is a prevalent, poorly understood condition that afflicts patients with a wide variety of diseases, including infections, malignancies, and rheumatologic disorders. It is characterized by a blunted erythropoietin response by erythroid precursors, decreased red blood cell survival, and a defect in iron absorption and macrophage iron retention, which interrupts iron delivery to erythroid precursor cells. We noted that patients with large hepatic adenomas had severe iron refractory anemia similar to that observed in anemia of chronic disease. This anemia resolved spontaneously after adenoma resection or liver transplantation. We investigated the role of the adenomas in the pathogenesis of the anemia and found that they produce inappropriately high levels of hepcidin mRNA. Hepcidin is a peptide hormone that has been implicated in controlling the release of iron from cells. We conclude that hepcidin plays a major, causative role in the anemia observed in our subgroup of patients with hepatic adenomas, and we speculate that it is important in the pathogenesis of the anemia of chronic disease in general.
引用
收藏
页码:3776 / 3781
页数:6
相关论文
共 26 条
[1]   Iron homeostasis: Insights from genetics and animal models [J].
Andrews, NC .
NATURE REVIEWS GENETICS, 2000, 1 (03) :208-217
[2]   Medical progress: Disorders of iron metabolism [J].
Andrews, NC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (26) :1986-1995
[3]  
Chen Y.-T., 2001, METABOLIC MOL BASIS, VI, P1521
[4]   EFFECT OF ENDOTOXIN ON IRON ABSORPTION [J].
CORTELL, S ;
CONRAD, ME .
AMERICAN JOURNAL OF PHYSIOLOGY, 1967, 213 (01) :43-&
[5]  
Fleming MD, 1997, NAT GENET, V16, P383, DOI 10.1038/ng0897-383
[6]   Hepcidin: A putative iron-regulatory hormone relevant to hereditary hemochromatosis and the anemia of chronic disease [J].
Fleming, RE ;
Sly, WS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8160-8162
[7]   CDC25 PHOSPHATASES AS POTENTIAL HUMAN ONCOGENES [J].
GALAKTIONOV, K ;
LEE, AK ;
ECKSTEIN, J ;
DRAETTA, G ;
MECKLER, J ;
LODA, M ;
BEACH, D .
SCIENCE, 1995, 269 (5230) :1575-1577
[8]   Iron, infections, and anemia of inflammation [J].
Jurado, RL .
CLINICAL INFECTIOUS DISEASES, 1997, 25 (04) :888-895
[9]   LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity [J].
Krause, A ;
Neitz, S ;
Mägert, HJ ;
Schulz, A ;
Forssmann, WG ;
Schulz-Knappe, P ;
Adermann, K .
FEBS LETTERS, 2000, 480 (2-3) :147-150
[10]  
LEE GR, 1983, SEMIN HEMATOL, V20, P61