Maternal Hepcidin Is Associated with Placental Transfer of Iron Derived from Dietary Heme and Nonheme Sources

被引:84
作者
Young, Melissa E. [1 ]
Griffin, Ian [2 ]
Pressman, Eva [3 ]
McIntyre, Allison W. [3 ]
Cooper, Elizabeth [3 ]
McNanley, Thomas [3 ]
Harris, Z. Leah [4 ]
Westerman, Mark [5 ]
O'Brien, Kimberly O. [1 ]
机构
[1] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[2] Baylor Coll Med, USDA, ARS, Childrens Nutr Res Ctr, Houston, TX 77030 USA
[3] Univ Rochester, Sch Med, Rochester, NY USA
[4] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[5] Intrins Life Sci LLC, La Jolla, CA USA
关键词
SUBGROUP C RECEPTOR; FERRITIN CONCENTRATIONS; DIABETIC PREGNANCIES; SERUM HEPCIDIN; ABSORPTION; DEFICIENCY; EXPRESSION; FETAL; ADOLESCENTS; HEMOGLOBIN;
D O I
10.3945/jn.111.145961
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
The determinants of placental transport of dietary iron remain largely uncharacterized. The objective of this research was to elucidate determinants of fetal Fe transfer from maternally ingested dietary heme and non-heme Fe. The study was undertaken in 19 pregnant females (16-32 y) who ingested intrinsically labeled Fe-58-heme and a nonheme Fe source ((FeSO4)-Fe-57) during the third trimester of pregnancy. At delivery, maternal and cord blood was obtained to assess neonatal Fe-57 and Fe-58 enrichment as a function of maternal/neonatal Fe status (serum ferritin (SF), transferrin receptor, hemoglobin (Hb), total body Fe, and hepcidin). There was a greater percentage of maternally absorbed Fe-58 tracer present in the neonates compared to the Fe-57 tracer (5.4 +/- 2.4 vs. 4.0 +/- 1.6; P < 0.0001). Net dietary nonheme Fe (mg) and heme Fe (mg) transferred to the fetus were both inversely correlated with measures of maternal serum hepcidin (P = 0.002, r(2) = 0.43; P= 0.004, r(2) = 0.39) and SF (P = 0.0008, r(2) = 0.49; P = 0.003, r(2) = 0.41) and directly associated with neonatal Hb (P= 0.004, r(2) = 0.39; P = 0.008, r(2) = 0.35). The results of this study suggest that during pregnancy there appears to be preferential fetal use of maternally ingested Fe derived from a dietary, animal-based heme source compared to Fe ingested as ferrous sulfate. Maternal serum hepcidin and maternal/neonatal Fe status may play a role in placental uptake of dietary heme and nonheme Fe. J. Nutr. 142: 33-39, 2012.
引用
收藏
页码:33 / 39
页数:7
相关论文
共 45 条
[1]  
Allen LH, 2005, AM J CLIN NUTR, V81, p1206S
[2]  
BROWN EB, 1968, J LAB CLIN MED, V72, P58
[3]   Hemoglobin concentrations influence birth outcomes in pregnant African-American adolescents [J].
Chang, SC ;
O'Brien, KO ;
Nathanson, MS ;
Mancini, J ;
Witter, FR .
JOURNAL OF NUTRITION, 2003, 133 (07) :2348-2355
[4]   The quantitative assessment of body iron [J].
Cook, JD ;
Flowers, CH ;
Skikne, BS .
BLOOD, 2003, 101 (09) :3359-3364
[5]   IRON-DEFICIENCY AND THE IMMUNE-RESPONSE [J].
DALLMAN, PR .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1987, 46 (02) :329-334
[6]   Production of stable-isotope-labeled bovine heme and its use to measure heme-iron absorption in children [J].
Etcheverry, Paz ;
Carstens, Gordon E. ;
Brown, Erin ;
Hawthorne, Keli M. ;
Chen, Zhensheng ;
Griffin, Ian J. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2007, 85 (02) :452-459
[7]   IRON-ABSORPTION FROM INFANT FOODS [J].
FOMON, SJ ;
ZIEGLER, EE ;
ROGERS, RR ;
NELSON, SE ;
EDWARDS, BB ;
GUY, DG ;
ERVE, JC ;
JANGHORBANI, M .
PEDIATRIC RESEARCH, 1989, 26 (03) :250-254
[8]   Effect of iron deficiency on placental transfer of iron and expression of iron transport proteins in vivo and in vitro [J].
Gambling, L ;
Danzeisen, R ;
Gair, S ;
Lea, RG ;
Charania, Z ;
Solanky, N ;
Joory, KD ;
Srai, SKS ;
McArdle, HJ .
BIOCHEMICAL JOURNAL, 2001, 356 :883-889
[9]   Fetal iron status regulates maternal iron metabolism during pregnancy in the rat [J].
Gambling, Lorraine ;
Czopek, Alicja ;
Andersen, Henriette S. ;
Holtrop, Grietje ;
Srai, S. Kaila S. ;
Krejpcio, Zbigniew ;
McArdle, Harry J. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2009, 296 (04) :R1063-R1070
[10]   Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation [J].
Ganz, T .
BLOOD, 2003, 102 (03) :783-788