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

被引:95
作者
Young, Melissa F. [1 ]
Glahn, Raymond P. [2 ]
Ariza-Nieto, Magnolia [2 ]
Inglis, Jeremy [1 ]
Olbina, Gordana [3 ]
Westerman, Mark [3 ]
O'Brien, Kimberly O. [1 ]
机构
[1] Cornell Univ, Div Nutr Sci, Ithaca, NY 14850 USA
[2] Agr Res Serv, Robert W Holley Ctr Agr & Hlth, USDA, Ithaca, NY USA
[3] Intrins LifeSci LLC, La Jolla, CA USA
关键词
FLESHED SWEET-POTATO; HEREDITARY HEMOCHROMATOSIS; MASS-SPECTROMETRY; BETA-CAROTENE; PRO-HEPCIDIN; BODY IRON; EXPRESSION; CHILDREN; INFLAMMATION; ANEMIA;
D O I
10.3945/ajcn.2008.26589
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
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 Fe-58 as FeSO4) and 6.8 mg 57 Fe 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. Am J Clin Nutr 2009; 89: 533-8.
引用
收藏
页码:533 / 538
页数:6
相关论文
共 37 条
[1]   Absorption by 1-year-old children of an iron supplement given with cow's milk or juice [J].
Abrams, SA ;
OBrien, KO ;
Wen, JP ;
Liang, LK ;
Stuff, JE .
PEDIATRIC RESEARCH, 1996, 39 (01) :171-175
[2]   APPLICATION OF MAGNETIC-SECTOR THERMAL IONIZATION MASS-SPECTROMETRY TO STUDIES OF ERYTHROCYTE IRON INCORPORATION IN SMALL CHILDREN [J].
ABRAMS, SA ;
WEN, JP ;
OBRIEN, KO ;
STUFF, JE ;
LIANG, LK .
BIOLOGICAL MASS SPECTROMETRY, 1994, 23 (12) :771-775
[3]   Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis [J].
Bridle, KR ;
Frazer, DM ;
Wilkins, SJ ;
Dixon, JL ;
Purdie, DM ;
Crawford, DHG ;
Subramaniam, VN ;
Powell, LW ;
Anderson, GJ ;
Ramm, GA .
LANCET, 2003, 361 (9358) :669-673
[4]  
*CDCP, 2008, NAT REP BIOCH IND DI
[5]   The quantitative assessment of body iron [J].
Cook, JD ;
Flowers, CH ;
Skikne, BS .
BLOOD, 2003, 101 (09) :3359-3364
[6]   Serum hepcidin in clinical specimens [J].
Dallalio, G ;
Fleury, T ;
Means, RT .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 122 (06) :996-1000
[7]   COMPOSITION OF SOME TROPICAL TUBEROUS FOODS [J].
EKPENYONG, TE .
FOOD CHEMISTRY, 1984, 15 (01) :31-36
[8]   Hepcidin expression inversely correlates with the expression of duodenal iron transporters and iron absorption in rats [J].
Frazer, DM ;
Wilkins, SJ ;
Becker, EM ;
Vulpe, CD ;
McKie, AT ;
Trinder, D ;
Anderson, GJ .
GASTROENTEROLOGY, 2002, 123 (03) :835-844
[9]  
GANZ T, 2008, BLOOD 0808, DOI DOI 10.1182/BL00D-2008-02-139915
[10]   Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound iron [J].
Gehrke, SG ;
Kulaksiz, H ;
Herrmann, T ;
Riedel, HD ;
Bents, K ;
Veltkamp, C ;
Stremmel, W .
BLOOD, 2003, 102 (01) :371-376