课题基金 / 基金详情

LEAD MOBILIZATION DURING PREGNANCY AND LACTATION

LEAD MOBILIZATION DURING PREGNANCY AND LACTATION
怀孕和哺乳期间的导线动员
批准号:
6578812
负责人:
Jacqueline Moline
金额:
$8.37万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2003-03-31

项目摘要

项目成果

Jacqueline Moline的其他基金

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中文摘要
翻译
描述(摘自应用程序) 来自病例报告和铅同位素比值研究的证据表明, 储存在骨骼中的铅在怀孕和哺乳期间被调动, 使母亲,特别是发育中的胎儿和婴儿处于危险之中 铅中毒胎盘对铅是完全可渗透的, 存在于母乳中。钙的摄入可以防止铅的吸收。 为了研究骨骼铅在 怀孕,也许更重要的是在哺乳期,我们建议 对一名儿童血铅和骨铅重复测定的干预研究 在墨西哥莫雷洛斯,环境铅暴露水平较高的妇女人口。 妇女将被随机接受钙和维生素补充剂,钙 没有维生素补充剂,或者只补充维生素。我们将 同时跟踪一组未怀孕妇女。我们假设 由于铅在怀孕和哺乳期间被动员,母体、胎儿和 婴儿血铅水平会增加,母亲骨铅水平会增加 减少。我们将比较骨铅和全血铅水平, 怀孕两周,六周, 产后12个月。将通过X射线测量骨铅水平 荧光。我们将检查骨转换的分子生物标志物, 评估是否同时发生骨重建和电极导线松动。我们 假设骨铅水平在怀孕期间会下降,并进一步 在哺乳期由于骨铅动员。对照组 非怀孕妇女将使我们能够比较骨铅的自然史, 没有怀孕和哺乳的变化。血铅水平 在每个孩子的同时,母亲的产后评估将 提供关于母亲将循环中的铅转移给孩子的信息。 为了评估基因与环境的相互作用,我们将研究多态性是否 在ALA-D中,血色素沉着症基因和维生素D受体影响铅 从骨头里解放出来。我们假设接受钙补充剂的女性 将有更少的铅动员,从而减少转移到他们的发展中国家, 孩子我们还将评估钙加维生素补充剂是否更有效, 比单独的钙更有保护作用。这项研究将在莫雷洛斯进行, 墨西哥的人口环境铅暴露率很高, 主要是通过使用铅釉陶瓷, 母乳喂养率高。这样我们就可以比较骨铅 哺乳期间的动员与妊娠期间发生的动员相同。的 调查应提供重要的见解,潜在的健康 慢性环境铅暴露对孕妇和哺乳期妇女的影响 妇女、发育中的胎儿和婴儿通过母乳喂养,以及 深入了解预防方法。
英文摘要
DESCRIPTION (Taken from application) Evidence from case reports and studies of lead isotope ratios suggest that lead stored in the skeleton is mobilized during pregnancy and lactation, placing the mother and, in particular, the developing fetus and infant at risk of lead poisoning. The placenta is fully permeable to lead, and lead is present in breast milk. Calcium intake may protect against lead absorption. To investigate the hypothesis that skeletal lead is mobilized during pregnancy, and perhaps more importantly during lactation, we propose an intervention study with repeated measures of blood and bone lead in a population of women in Morelos, Mexico with high environmental lead exposure. Women will be randomized to receive calcium and vitamin supplements, calcium without vitamin supplements, or vitamin supplements alone. We will simultaneously follow a control group of non-pregnant women. We hypothesize that as lead is mobilized during pregnancy and lactation, maternal, fetal and infant blood-lead levels will increase, and maternal bone-lead levels will decrease. We will compare bone- and whole blood-lead levels prior to pregnancy with measurements obtained from the same women at two weeks, six months and twelve months postpartum. Bone-lead levels will be measured by X-Ray Fluorescence. We will examine molecular biomarkers of bone turnover to assess whether concurrent bone remodeling and lead mobilization occurs. We hypothesize that bone-lead levels will decrease during pregnancy, and further during lactation as a result of bone-lead mobilization. The control group of non-pregnancy women will allow us to compare the natural history of bone-lead changes in the absence of pregnancy and lactation. Blood-lead levels obtained in each child at the same time as the mother s postpartum evaluations will provide information about maternal transfer of circulating lead to the child. To assess gene-environment interactions, we will examine whether polymorphisms in ALA-D, the hemochromatosis gene and the Vitamin D receptor influence lead release from bone. We hypothesize that women receiving calcium supplements will have less lead mobilization and thus less transfer to their developing child. We will also assess whether calcium plus vitamin supplements is more protective than calcium alone. This study will be undertaken in Morelos, Mexico where the population has high environmental lead exposure, predominantly through the use of lead-glazed ceramics, and where women have high rates of breast-feeding. Thus we will be able to compare bone-lead mobilization during lactation with that which occurs during pregnancy. The investigation should provide important insights into the potential health effects of chronic environmental lead exposure to pregnant and lactating women, developing fetuses, and infants through breast feeding, as well as insights into approaches for prevention.
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