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Received on February 10, 2006
Accepted on March 24, 2006
Review |
1 Department of Clinical Chemistry, Radboud University Nijmegen Medical Centre, Nijmegen.
2 Department of General Internal Medicine, Radboud University Nijmegen Medical Centre, Nijmegen.
3 Department of Clinical Chemistry, Radboud University Nijmegen Medical Centre, Nijmegen. and Eijkman-Winkler Institute, University Medical Centre Utrecht, Utrecht, The Netherlands.
* To whom correspondence should be addressed. E-mail: D.Swinkels{at}akc.umcn.nl.
Since the discovery of the hemochromatosis gene (HFE) in 1996, several novel gene defects have been detected, explaining the mechanism and diversity of iron-overload diseases. At least 4 main types of hereditary hemochromatosis (HH) have been identified. Surprisingly, genes involved in HH encode for proteins that all affect pathways centered around liver hepcidin synthesis and its interaction with ferroportin, an iron exporter in enterocytes and macrophages. Hepcidin concentrations in urine negatively correlate with the severity of HH. Cytokine-mediated increases in hepcidin appear to be an important causative factor in anemia of inflammation, which is characterized by sequestration of iron in the macrophage system. For clinicians, the challenge is now to diagnose HH before irreversible damage develops and, at the same time, to distinguish progressive iron overload from increasingly common diseases with only moderately increased body iron stores, such as the metabolic syndrome. Understanding the molecular regulation of iron homeostasis may be helpful in designing innovative and reliable DNA and protein tests for diagnosis. Subsequently, evidence-based diagnostic strategies must be developed, using both conventional and innovative laboratory tests, to differentiate between the various causes of distortions of iron metabolism. This review describes new insights in mechanisms of iron overload, which are needed to understand new developments in diagnostic medicine.
The following articles in journals at HighWire Press have cited this article:
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K. S. Olsson and A. Norrby Comment to: Hepcidin: from discovery to differential diagnosis. Haematologica 2008; 93:90-7 Haematologica, June 1, 2008; 93(6): e51 - e51. [Full Text] [PDF] |
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E. H.J.M. Kemna, H. Tjalsma, H. L. Willems, and D. W. Swinkels Hepcidin: from discovery to differential diagnosis Haematologica, January 1, 2008; 93(1): 90 - 97. [Abstract] [Full Text] [PDF] |
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E. H.J.M. Kemna, H. Tjalsma, V. N. Podust, and D. W. Swinkels Mass Spectrometry-Based Hepcidin Measurements in Serum and Urine: Analytical Aspects and Clinical Implications Clin. Chem., April 1, 2007; 53(4): 620 - 628. [Abstract] [Full Text] [PDF] |
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M. V. Verga Falzacappa, M. Vujic Spasic, R. Kessler, J. Stolte, M. W. Hentze, and M. U. Muckenthaler STAT3 mediates hepatic hepcidin expression and its inflammatory stimulation Blood, January 1, 2007; 109(1): 353 - 358. [Abstract] [Full Text] [PDF] |
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