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Am J Clin Nutr 89: 533-538, 2009. First published December 10, 2008; doi:10.3945/ajcn.2008.26589
American Journal of Clinical Nutrition, doi:10.3945/ajcn.2008.26589
Vol. 89, No. 2, 533-538, February 2009

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© 2009 American Society for Clinical Nutrition

ORIGINAL RESEARCH COMMUNICATION

Serum hepcidin is significantly associated with iron absorption from food and supplemental sources in healthy young women

Melissa F Young1,2,3, Raymond P Glahn1,2,3, Magnolia Ariza-Nieto1,2,3, Jeremy Inglis1,2,3, Gordana Olbina1,2,3, Mark Westerman1,2,3 and Kimberly O O'Brien1,2,3

1 From the Division of Nutritional Sciences, Cornell University, Ithaca NY (MFY, JI, and KOO); Robert W Holley Center for Agriculture and Health, US Department of Agriculture, Agriculture Research Service, Ithaca NY (RPG and MA-N); and the Intrinsic LifeSciences, LLC, La Jolla, CA (GO and MW).

2 Supported by an agreement with Cornell University, Division of Nutritional Sciences, under USDA/CSREES 3995979 and 399410.

3 Address reprint requests and correspondence to KO O'Brien, Cornell University, Division of Nutritional Sciences, MVR 340, Ithaca, NY 14850. E-mail: koo4{at}cornell.edu.

Background: Hepcidin is a key regulator of iron homeostasis, but to date no studies have examined the effect of hepcidin on iron absorption in humans.

Objective: Our objective was to assess relations between both serum hepcidin and serum prohepcidin with nonheme-iron absorption in the presence and absence of food with the use of dual stable-iron-isotope techniques.

Design: The study group included 18 healthy nonpregnant women. Women received in random order a supplemental iron source (7.6 mg FeSO4 providing 0.9 mg 58Fe as FeSO4) and 6.8 mg 57Fe ferrous sulfate tracer administered with a nonheme food source [orange-fleshed sweet potato (OFSP): 1.4 mg native Fe]. Iron absorption was determined by analyzing blood samples taken 14 d after dosing with the use of magnetic sector thermal ionization mass spectrometry. Serum hepcidin was assessed by a new competitive serum enzyme-linked immunosorbent assay (ELISA) specific for the refolded, mature 25–amino acid form, and serum prohepcidin was assessed by an ELISA specific for amino acids 28–47 of the hepcidin prohormone.

Results: In these women, iron absorption averaged 14.71 ± 10.7% from the supplemental iron compared with 3.63 ± 6.5% from the OFSP. Absorption of nonheme iron assessed in the presence (P = 0.038) and absence (P = 0.0296) of food was significantly associated with serum hepcidin but was not significantly related to serum prohepcidin.

Conclusion: Serum hepcidin, but not prohepcidin, was inversely associated with iron absorption from supplemental and food-based nonheme-iron sources in iron-replete healthy women.


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