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环境污染物对胎儿影响的分子流行病学研究。

Molecular epidemiologic research on the effects of environmental pollutants on the fetus.

作者信息

Perera F P, Jedrychowski W, Rauh V, Whyatt R M

机构信息

Joseph L. Mailman School of Public Health at Columbia University, New York, NY 10032, USA.

出版信息

Environ Health Perspect. 1999 Jun;107 Suppl 3(Suppl 3):451-60. doi: 10.1289/ehp.99107s3451.

Abstract

Evidence shows that fetuses and infants are more affected than adults by a variety of environmental toxicants because of differential exposure, physiologic immaturity, and a longer lifetime over which disease initiated in early life can develop. In this article we review data on the effects of in utero exposure to common environmental contaminants, including polycyclic aromatic hydrocarbons (PAH), particulate matter and environmental tobacco smoke (ETS). We then summarize results from our molecular epidemiologic study to assess risks from in utero exposures to ambient air pollution and ETS. This research study, conducted in Poland, used biomarkers to measure the internal and bioeffective dose of toxicants and individual susceptibility factors. The study included 160 mothers and 160 newborns. Ambient air pollution was significantly associated (p= 0.05) with the amount of PAH bound to DNA (PAH-DNA adducts) in both maternal and infant cord white blood cells (WBC). Newborns with elevated PAH-DNA adducts (greater than the median) had significantly decreased birth weight (p= 0.05), birth length (p= 0.02), and head circumference (p= 0.0005) compared to the newborns with lower adducts (n= 135). Maternal and infant cotinine levels were increased by active and passive cigarette smoke exposure of the mother (p= 0.01). An inverse correlation was seen between newborn plasma cotinine (nanograms per milliliter) and birth weight (p= 0.0001) and length (p= 0.003). Adducts were elevated in placental tissue and WBC of newborns who were heterozygous or homozygous for the cytochrome P4501A1 MspI restriction fragment length polymorphism (RFLP) compared to newborns without the RFLP. Levels of PAH-DNA and cotinine were higher in newborns than mothers. These results document that there is significant transplacental transfer of PAH and ETS constituents from mother to fetus; that PAH-DNA adduct levels in maternal and newborn WBC were increased with environmental exposure to PAH from ambient pollution; and that the fetus is more sensitive to genetic damage than the mother. The study also provided the first molecular evidence that transplacental PAH exposure to the fetus is compromising fetal development. If confirmed, these findings could have significant public health implications since a number of studies have found that reduction of head circumference at birth correlates with lower intelligence quotient as well as poorer cognitive functioning and school performance in childhood.

摘要

有证据表明,由于暴露情况不同、生理不成熟以及早年引发的疾病发展所需的更长生存期,胎儿和婴儿比成年人更容易受到各种环境毒物的影响。在本文中,我们回顾了关于子宫内暴露于常见环境污染物(包括多环芳烃(PAH)、颗粒物和环境烟草烟雾(ETS))影响的数据。然后,我们总结了分子流行病学研究的结果,以评估子宫内暴露于环境空气污染和ETS的风险。这项在波兰进行的研究使用生物标志物来测量毒物的内部和生物有效剂量以及个体易感性因素。该研究包括160名母亲和160名新生儿。环境空气污染与母亲和婴儿脐带白细胞(WBC)中与DNA结合的PAH量(PAH-DNA加合物)显著相关(p = 0.05)。与加合物水平较低的新生儿(n = 135)相比,PAH-DNA加合物水平升高(高于中位数)的新生儿出生体重显著降低(p = 0.05)、出生身长显著降低(p = 0.02)、头围显著降低(p = 0.0005)。母亲主动和被动吸烟会增加母婴可替宁水平(p = 0.01)。新生儿血浆可替宁(纳克/毫升)与出生体重(p = 0.0001)和身长(p = 0.003)之间呈负相关。与没有细胞色素P4501A1 MspI限制性片段长度多态性(RFLP)的新生儿相比,具有细胞色素P4501A1 MspI RFLP杂合或纯合的新生儿胎盘组织和WBC中的加合物水平升高。新生儿的PAH-DNA和可替宁水平高于母亲。这些结果证明,PAH和ETS成分存在从母亲到胎儿的显著胎盘转移;母亲和新生儿WBC中的PAH-DNA加合物水平随着环境中PAH暴露而增加;并且胎儿比母亲对基因损伤更敏感。该研究还提供了首个分子证据,即胎儿经胎盘暴露于PAH会损害胎儿发育。如果得到证实,这些发现可能具有重大的公共卫生意义,因为多项研究发现出生时头围减小与较低的智商以及儿童期较差的认知功能和学业成绩相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5d4/1566212/5f9992f8247a/envhper00520-0069-a.jpg

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