Centre of Exellence for Nutrition (CEN), North-West University, Potchefstroom, South Africa.
Int J Obes (Lond). 2013 Jan;37(1):24-30. doi: 10.1038/ijo.2012.145. Epub 2012 Sep 4.
Many countries in the nutrition transition have high rates of iron deficiency (ID) and overweight (OW). ID is more common in OW children; this may be due to adiposity-related inflammation reducing iron absorption.
We investigated whether weight status predicts response to oral iron supplementation in ID South African children.
A placebo-controlled trial of oral iron supplementation (50 mg, 4 × weeks for 8.5 months) was done in ID 6- to 11-year-old children (n=321); 28% were OW or obese. BMI-for-age z-scores (BAZ), hepcidin (in a sub-sample), hemoglobin, serum ferritin (SF), transferrin receptor (TfR), zinc protoporphyrin (ZnPP) and C-reactive protein (CRP) were measured; body iron was calculated from the SF to TfR ratio.
At baseline, BAZ correlated with CRP (r=0.201, P<0.001) and CRP correlated with hepcidin (r=0.384, P<0.001). Normal weight children supplemented with iron had significantly lower TfR concentrations at endpoint than the OW children supplemented with iron and the children receiving placebo. Higher BAZ predicted higher TfR (β=0.232, P<0.001) and lower body iron (β=-0.090, P=0.016) at endpoint, and increased the odds ratio (OR) for remaining ID at endpoint in both the iron and placebo groups (iron: OR 2.31, 95% CI: 1.13, 4.73; placebo: OR 1.78, 95% CI: 1.09, 2.91). In the children supplemented with iron, baseline hepcidin and BAZ were significant predictors of endpoint TfR, with a trend towards a hepcidin × BAZ interaction (P=0.058).
South African children with high BAZ have a two-fold higher risk of remaining ID after iron supplementation. This may be due to their higher hepcidin concentrations reducing iron absorption. Thus, the current surge in OW in rapidly developing countries may undercut efforts to control anemia in vulnerable groups. The trial is registered at clinicaltrials.gov as NCT01092377.
许多处于营养转型期的国家缺铁(ID)和超重(OW)的发生率都很高。OW 儿童中 ID 更为常见;这可能是由于肥胖相关炎症降低了铁的吸收。
我们研究了南非 ID 儿童的体重状况是否预测口服铁补充的反应。
对 6-11 岁 ID 儿童(n=321)进行了为期 8.5 个月的 4 次每周口服铁补充(50mg)的安慰剂对照试验;28%为 OW 或肥胖。测量 BMI 年龄 z 评分(BAZ)、铁调素(亚样本)、血红蛋白、血清铁蛋白(SF)、转铁蛋白受体(TfR)、锌原卟啉(ZnPP)和 C 反应蛋白(CRP);根据 SF 与 TfR 的比值计算体内铁含量。
在基线时,BAZ 与 CRP 相关(r=0.201,P<0.001),CRP 与铁调素相关(r=0.384,P<0.001)。与补充铁的 OW 儿童和接受安慰剂的儿童相比,正常体重儿童补充铁后 TfR 浓度在终点显著降低。较高的 BAZ 预测终点时 TfR 更高(β=0.232,P<0.001)和体内铁更少(β=-0.090,P=0.016),并增加了铁和安慰剂组中终点 ID 持续存在的比值比(OR)(铁:OR 2.31,95%CI:1.13,4.73;安慰剂:OR 1.78,95%CI:1.09,2.91)。在补充铁的儿童中,基线铁调素和 BAZ 是终点 TfR 的显著预测因素,铁调素与 BAZ 的交互作用呈趋势(P=0.058)。
南非高 BAZ 的儿童在补充铁后仍有两倍的 ID 风险。这可能是由于他们较高的铁调素浓度降低了铁的吸收。因此,快速发展中国家目前 OW 的激增可能会削弱控制弱势群体贫血的努力。该试验在 clinicaltrials.gov 上注册为 NCT01092377。