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Research Article Free access | 10.1172/JCI113868

Duodenal iron proteins in idiopathic hemochromatosis.

P Whittaker, B S Skikne, A M Covell, C Flowers, A Cooke, S R Lynch, and J D Cook

Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Department of Medicine, Kansas University Medical Center, Kansas City 66103.

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Published January 1, 1989 - More info

Published in Volume 83, Issue 1 on January 1, 1989
J Clin Invest. 1989;83(1):261–267. https://doi.org/10.1172/JCI113868.
© 1989 The American Society for Clinical Investigation
Published January 1, 1989 - Version history
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Abstract

This study was undertaken to assess the relationship between iron absorption and the concentration of duodenal iron proteins in normal subjects and patients with idiopathic hemochromatosis (IH). Biopsies were obtained endoscopically from the duodenum in 17 normal subjects, 3 of whom were mildly iron deficient, and 7 patients with untreated IH. The absorption of both heme and nonheme iron was increased in IH despite a 20-fold elevation in serum ferritin. Immunoassays using MAb were used to measure transferrin, H-rich ferritin, and L-rich ferritin in mucosal samples. Mucosal transferrin concentrations in normal subjects did not correlate with either iron status or iron absorption, indicating that mucosal transferrin plays no physiological role in iron absorption. Mucosal transferrin was significantly lower in IH, presumably because of a decrease in mucosal transferrin receptors. Mucosal H and L ferritin concentrations were directly related to body iron stores and inversely related to iron absorption in normal subjects. In IH, mucosal H and L ferritin failed to increase in parallel with the serum ferritin, but were appropriate for the level of iron absorption. The relationship of mucosal H/L ferritin in IH did not differ from that observed in normal subjects. Our findings indicate that the major abnormality in duodenal iron proteins in IH is a parallel decrease in the concentration of H- and L-rich ferritin. It is not evident whether this is the result or the cause of the absorptive abnormality.

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