Swiss Federal Institute of Technology, Zurich, Switzerland.
Am J Clin Nutr. 2010 Mar;91(3):802-7. doi: 10.3945/ajcn.2009.28800. Epub 2009 Dec 16.
Iron absorption in humans is highly variable even after iron status and dietary components that influence iron absorption are controlled for. Inherited factors may help explain this variance.
Our objective was to compare nonheme-iron absorption from a noninhibitory, stable-isotope-labeled test meal in preschool-aged children and their mothers.
We provided 72 test meals based on degermed maize flour and milk powder and fortified with [(57)Fe]ferrous fumarate or [(58)Fe]ferrous sulfate to healthy Mexican preschool children [n = 18; mean (+/-SD) age: 3.6 +/- 1.0 y] and their mothers [n = 18; mean (+/-SD) age: 28.0 +/- 5.2 y]. Iron absorption was calculated on the basis of incorporation of isotopes into erythrocytes after 14 d and was adjusted for differences in iron status.
There was a wide variation in iron absorption from the test meals: in the mothers and children, the median fractional absorption of ferrous sulfate was 22.55% (range: 1.65-54.83%) and 5.51% (range: 2.23-17.20%), respectively (P < 0.0001). After adjustment for serum ferritin, the significant difference in absorption between mothers and their children disappeared. Despite this broad range of iron absorption, corrected fractional iron absorption from the ferrous fumarate-fortified (r(2) = 0.582) and the ferrous sulfate-fortified test meals (r(2) = 0.557) was strongly correlated in mothers and their children (P < 0.0001). There was a striking positive correlation between the mean corrected fractional iron absorption from both test meals in mothers and their children (r(2) = 0.782, P < 0.0001). In regression analyses that included age, sex, and hemoglobin, the only significant predictor of corrected fractional iron absorption in children was corrected fractional iron absorption in their mothers (standardized beta = 0.884, P < 0.001).
Nonheme-iron absorption exhibits a strong familial tendency. After differences in meal matrix and serum ferritin are accounted for, these data suggest that inheritance and/or shared environmental factors explain most of the variance in dietary iron absorption.
即使在控制了铁状态和影响铁吸收的饮食成分后,人体对非血红素铁的吸收仍然存在很大差异。遗传因素可能有助于解释这种差异。
我们的目的是比较学龄前儿童及其母亲从非抑制性、稳定同位素标记的测试餐中吸收非血红素铁。
我们为健康的墨西哥学龄前儿童(n=18;平均(+/-SD)年龄:3.6 +/- 1.0 岁)和他们的母亲(n=18;平均(+/-SD)年龄:28.0 +/- 5.2 岁)提供了基于去胚玉米粉和奶粉的 72 份测试餐,并添加了(57)Fe 富马酸亚铁或(58)Fe 硫酸亚铁。在 14 天后,通过将同位素掺入红细胞中来计算铁的吸收,并根据铁状态的差异进行调整。
测试餐中铁的吸收存在很大差异:母亲和儿童的硫酸亚铁的中位分数吸收率分别为 22.55%(范围:1.65-54.83%)和 5.51%(范围:2.23-17.20%)(P<0.0001)。在校正血清铁蛋白后,母亲和儿童之间的吸收差异消失。尽管铁吸收范围很广,但富马酸亚铁强化(r(2) = 0.582)和硫酸亚铁强化测试餐(r(2) = 0.557)的校正分数铁吸收在母亲及其子女中呈强相关性(P<0.0001)。母亲和儿童的两种测试餐的平均校正分数铁吸收之间存在显著正相关(r(2) = 0.782,P<0.0001)。在包括年龄、性别和血红蛋白的回归分析中,儿童校正分数铁吸收的唯一显著预测因子是其母亲的校正分数铁吸收(标准化β=0.884,P<0.001)。
非血红素铁吸收具有很强的家族倾向。在考虑到膳食基质和血清铁蛋白的差异后,这些数据表明遗传和/或共同的环境因素解释了饮食中铁吸收的大部分差异。