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母体居住的阿特拉津暴露与后代的鼻后孔闭锁和狭窄的风险。

Maternal residential atrazine exposure and risk for choanal atresia and stenosis in offspring.

机构信息

Human Genetics Center, Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, TX77030, USA.

出版信息

J Pediatr. 2013 Mar;162(3):581-6. doi: 10.1016/j.jpeds.2012.08.012. Epub 2012 Oct 1.

Abstract

OBJECTIVE

To assess the relationship between estimated residential maternal exposure to atrazine during pregnancy and the risk for choanal atresia or stenosis in offspring.

STUDY DESIGN

Data for 280 nonsyndromic cases and randomly selected, population-based controls delivered between 1999 and 2008 were obtained from the Texas Birth Defects Registry. County-level estimates of atrazine levels obtained from the US Geological Survey were assigned to cases and controls based on maternal county of residence at delivery. Unconditional logistic regression was used to assess the relationship between maternal residential atrazine exposure and the risk for choanal atresia or stenosis in offspring.

RESULTS

Compared with offspring of mothers with low levels of estimated residential atrazine exposure, those with high levels had nearly a 2-fold increase in risk for choanal atresia or stenosis (aOR, 1.79; 95% CI, 1.17-2.74). A significant linear trend was also observed with increasing levels of atrazine exposure (adjusted P = .002).

CONCLUSION

A link between maternal exposure to endocrine disruptors, such as atrazine, and the risk of choanal atresia is plausible based on previous findings. Our results lend further support to this hypothesis.

摘要

目的

评估妊娠期间母体估计的内吸磷暴露与后代发生后鼻孔闭锁或狭窄风险之间的关系。

研究设计

本研究的数据来自于德克萨斯州出生缺陷登记处,包括了 1999 年至 2008 年间的 280 例非综合征型病例和随机选择的基于人群的对照。根据产妇分娩时的居住地,将美国地质调查局获得的内吸磷水平的县一级估计值分配给病例和对照。采用非条件逻辑回归来评估母体居住内吸磷暴露与后代发生后鼻孔闭锁或狭窄风险之间的关系。

结果

与低水平母体居住内吸磷暴露的后代相比,高水平暴露的后代发生后鼻孔闭锁或狭窄的风险增加了近两倍(优势比,1.79;95%置信区间,1.17-2.74)。随着内吸磷暴露水平的增加,也观察到了显著的线性趋势(调整后的 P 值=0.002)。

结论

基于先前的研究结果,母体接触内分泌干扰物(如内吸磷)与后鼻孔闭锁风险之间存在关联是合理的。我们的研究结果进一步支持了这一假说。

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Otolaryngol Clin North Am. 2009 Apr;42(2):339-52, x. doi: 10.1016/j.otc.2009.01.001.
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