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

TitleInappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease.
Publication TypeJournal Article
Year of Publication2002
AuthorsWeinstein DA, Roy CN, Fleming MD, Loda MF, Wolfsdorf JI, Andrews NC
JournalBlood
Volume100
Issue10
Pagination3776-81
Date Published2002 Nov 15
ISSN0006-4971
KeywordsAdenoma, Liver Cell, Adolescent, Adult, Anemia, Iron-Deficiency, Anemia, Refractory, Animals, Antimicrobial Cationic Peptides, Chronic Disease, Female, Glycogen Storage Disease Type I, Hepcidins, Humans, Liver, Male, Mice, Mice, Mutant Strains, RNA, Messenger, RNA, Neoplasm, Up-Regulation
Abstract

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.

DOI10.1182/blood-2002-04-1260
Alternate JournalBlood
PubMed ID12393428
Grant ListK08-03600 / / PHS HHS / United States
M01RR02172 / RR / NCRR NIH HHS / United States
T32-HL07623-15 / HL / NHLBI NIH HHS / United States
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