Laboratories of Environmental Toxicology/Chemical Carcinogenesis, Chulabhorn Research Institute, Laksi, Bangkok, 10210, Thailand.
Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Ratchathewi, Bangkok, 10400, Thailand.
Environ Health. 2019 Jun 7;18(1):51. doi: 10.1186/s12940-019-0481-7.
Growing evidence indicates that in utero arsenic exposures in humans may increase the risk of adverse health effects and development of diseases later in life. This study aimed to evaluate potential health risks of in utero arsenic exposure on genetic damage in newborns in relation to maternal arsenic exposure.
A total of 205 pregnant women residing in arsenic-contaminated areas in Hanam province, Vietnam, were recruited. Prenatal arsenic exposure was determined by arsenic concentration in mother's toenails and urine during pregnancy and in umbilical cord blood collected at delivery. Genetic damage in newborns was assessed by various biomarkers of early genetic effects including oxidative/nitrative DNA damage (8-hydroxydeoxyguanosine, 8-OHdG, and 8-nitroguanine), DNA strand breaks and micronuclei (MN) in cord blood.
Maternal arsenic exposure, measured by arsenic levels in toenails and urine, was significantly increased (p < 0.05) in subjects residing in areas with high levels of arsenic contamination in drinking water. Cord blood arsenic level was significantly increased in accordance with maternal arsenic exposure (p < 0.001). Arsenic exposure in utero is associated with genotoxic effects in newborns indicated as increased levels of 8-OHdG, 8-nitroguanine, DNA strand breaks and MN frequency in cord blood with increasing levels of maternal arsenic exposure. Maternal toenail arsenic level was significantly associated with all biomarkers of early genetic effects, while cord blood arsenic levels associated with DNA strand breaks and MN frequency.
In utero arsenic exposure is associated with various types of genetic damage in newborns potentially contributing to the development of diseases, including cancer, later in life.
越来越多的证据表明,人类在子宫内接触砷可能会增加不良健康影响和晚年疾病发展的风险。本研究旨在评估与母体砷暴露相关的胎儿砷暴露对新生儿遗传损伤的潜在健康风险。
共招募了 205 名居住在越南汉喃省砷污染地区的孕妇。孕妇在怀孕期间和分娩时采集的脐带血中,通过母亲的脚趾甲和尿液中的砷浓度来确定产前砷暴露情况。通过各种早期遗传效应生物标志物评估新生儿的遗传损伤,包括氧化/硝化 DNA 损伤(8-羟基脱氧鸟苷、8-硝基鸟嘌呤)、DNA 链断裂和脐血微核(MN)。
母体砷暴露(通过脚趾甲和尿液中的砷水平测量)在饮用水中砷污染水平较高的地区的研究对象中显著增加(p < 0.05)。脐带血中的砷水平随着母体砷暴露的增加而显著增加(p < 0.001)。胎儿期的砷暴露与新生儿的遗传毒性效应有关,表现为随着母体砷暴露水平的增加,脐血中 8-OHdG、8-硝基鸟嘌呤、DNA 链断裂和 MN 频率的水平升高。母体脚趾甲中的砷水平与所有早期遗传效应的生物标志物显著相关,而脐带血中的砷水平与 DNA 链断裂和 MN 频率相关。
胎儿期砷暴露与新生儿的多种类型遗传损伤有关,这些损伤可能导致包括癌症在内的晚年疾病的发生。