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FETAL, NEONATAL AND CHILDHOOD EFFECTS OF IN UTERO EXPOSURE TO PCBS AND DDE

FETAL, NEONATAL AND CHILDHOOD EFFECTS OF IN UTERO EXPOSURE TO PCBS AND DDE
子宫内接触 PCB 和 DDE 对胎儿、新生儿和儿童的影响
批准号:
6432605
负责人:
Mark A. Klebanoff
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:

项目摘要

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中文摘要
翻译
子宫内暴露于有机氯化合物的长期影响具有重要的潜在意义。这些化合物在全世界几乎100%的人体内都能检测到,它们与儿童神经发育迟缓有关。此外,滴滴涕的主要代谢物p,p'-DDE是一种弱雌激素,在人体中观察到的浓度是雄激素受体阻滞剂。该项目的目的之一是确定妊娠期间获得的母体血清DDE浓度是否是男性后代隐睾、尿道下裂和多毛症的危险因素。选择这些畸形是因为它们是子宫内雄激素活性不足的标志。其他目的是确定子宫内暴露于DDE是否随后与青春期女性月经初潮年龄的改变和青春期男性肥胖风险的增加有关,以及子宫内暴露于多氯联苯是否与儿童期肌肉张力、反射、智商和听力的次优相关。迄今为止的工作表明,这些化合物可以在相关浓度下从研究人群中恢复,并且这些化合物在妊娠早期和晚期血清中的浓度之间的相关性足够高,可以使用妊娠晚期血清作为妊娠早期暴露的替代品。主要研究的血清DDE和多氯联苯浓度分析始于2000年。青少年结果的血清分析将于2001财年开始。
英文摘要
The long-term effects of in utero exposure to organochlorine compounds is of great potential importance. These compounds, which are detectable in nearly 100% of humans worldwide, have been linked to reduced neurodevelopment in children. In addition, p,p'-DDE, the primary metabolite of DDT, is a weak estrogen, and an androgen receptor blocker at concentrations observed in humans. One objective of this project is to determine whether maternal serum concentration of DDE, obtained during pregnancy, is a risk factor for cryptorchidism, hypospadias and polythelia in male offspring. These malformations were chosen because they are markers of deficient androgen activity in utero. Other objectives are to determine whether in utero exposure to DDE is subsequently associated with an altered age at menarche in adolescent females and an increased risk of obesity in adolescent males, and whether in utero exposure to PCBs is associated with suboptimal muscle tone, reflexes, IQ and hearing during childhood. Work to date has demonstrated that these compounds can be recovered from the study population at relevant concentrations, and that the correlation between concentrations of these compounds in first and third trimester serum is sufficiently high to employ third-trimester serum as a surrogate for first-trimester exposure. Analysis of the concentrations of DDE and PCBs in serum for the main study began in FY 00. Serum analysis for the adolescent outcomes will begin in FY 01.
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