Laboratório de Toxicologia e Essencialidade de Metais, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo 14040-903, Brazil; Wadsworth Center, New York State Department of Health, and Department of Environmental Health Sciences, School of Public Health, State University of New York at Albany, New York 12201, United States.
Wadsworth Center, New York State Department of Health, and Department of Environmental Health Sciences, School of Public Health, State University of New York at Albany, New York 12201, United States; Department of Chemistry, The Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway.
Environ Int. 2018 Jul;116:269-277. doi: 10.1016/j.envint.2018.04.023. Epub 2018 Apr 25.
Human exposure to endocrine disrupting chemicals (EDCs) has received considerable attention over the last three decades. However, little is known about the influence of co-exposure to multiple EDCs on effect-biomarkers such as oxidative stress in Brazilian children. In this study, concentrations of 40 EDCs were determined in urine samples collected from 300 Brazilian children of ages 6-14 years and data were analyzed by advanced data mining techniques. Oxidative DNA damage was evaluated from the urinary concentrations of 8-hydroxy-2'-deoxyguanosine (8OHDG). Fourteen EDCs, including bisphenol A (BPA), methyl paraben (MeP), ethyl paraben (EtP), propyl paraben (PrP), 3,4-dihydroxy benzoic acid (3,4-DHB), methyl-protocatechuic acid (OH-MeP), ethyl-protocatechuic acid (OH-EtP), triclosan (TCS), triclocarban (TCC), 2-hydroxy-4-methoxybenzophenone (BP3), 2,4-dihydroxybenzophenone (BP1), bisphenol A bis(2,3-dihydroxypropyl) glycidyl ether (BADGE·2HO), 2,4-dichlorophenol (2,4-DCP), and 2,5-dichlorophenol (2,5-DCP) were found in >50% of the urine samples analyzed. The highest geometric mean concentrations were found for MeP (43.1 ng/mL), PrP (3.12 ng/mL), 3,4-DHB (42.2 ng/mL), TCS (8.26 ng/mL), BP3 (3.71 ng/mL), and BP1 (4.85 ng/mL), and exposures to most of which were associated with personal care product (PCP) use. Statistically significant associations were found between urinary concentrations of 8OHDG and BPA, MeP, 3,4-DHB, OH-MeP, OH-EtP, TCS, BP3, 2,4-DCP, and 2,5-DCP. After clustering the data on the basis of i) 14 EDCs (exposure levels), ii) demography (age, gender and geographic location), and iii) 8OHDG (effect), two distinct clusters of samples were identified. 8OHDG concentration was the most critical parameter that differentiated the two clusters, followed by OH-EtP. When 8OHDG was removed from the dataset, predictability of exposure variables increased in the order of: OH-EtP > OH-MeP > 3,4-DHB > BPA > 2,4-DCP > MeP > TCS > EtP > BP1 > 2,5-DCP. Our results showed that co-exposure to OH-EtP, OH-MeP, 3,4-DHB, BPA, 2,4-DCP, MeP, TCS, EtP, BP1, and 2,5-DCP was associated with DNA damage in children. This is the first study to report exposure of Brazilian children to a wide range of EDCs and the data mining approach further strengthened our findings of chemical co-exposures and biomarkers of effect.
人类接触内分泌干扰化学物质(EDCs)在过去三十年中受到了相当大的关注。然而,对于多种 EDC 共同暴露对巴西儿童氧化应激等效应生物标志物的影响知之甚少。在这项研究中,对 300 名年龄在 6-14 岁的巴西儿童的尿液样本中检测了 40 种 EDCs 的浓度,并通过先进的数据挖掘技术对数据进行了分析。通过尿中 8-羟基-2'-脱氧鸟苷(8OHDG)的浓度来评估氧化 DNA 损伤。在分析的尿液样本中发现了 14 种 EDC,包括双酚 A(BPA)、甲基对羟基苯甲酸酯(MeP)、乙基对羟基苯甲酸酯(EtP)、丙基对羟基苯甲酸酯(PrP)、3,4-二羟基苯甲酸(3,4-DHB)、甲基-原儿茶酸(OH-MeP)、乙基-原儿茶酸(OH-EtP)、三氯生(TCS)、三氯卡班(TCC)、2-羟基-4-甲氧基二苯甲酮(BP3)、2,4-二羟基二苯甲酮(BP1)、双酚 A 双(2,3-二羟基丙基)缩水甘油醚(BADGE·2HO)、2,4-二氯苯酚(2,4-DCP)和 2,5-二氯苯酚(2,5-DCP)。MeP(43.1ng/mL)、PrP(3.12ng/mL)、3,4-DHB(42.2ng/mL)、TCS(8.26ng/mL)、BP3(3.71ng/mL)和 BP1(4.85ng/mL)的几何平均浓度最高,这些物质的暴露大多与个人护理产品(PCP)的使用有关。尿中 8OHDG 浓度与 BPA、MeP、3,4-DHB、OH-MeP、OH-EtP、TCS、BP3、2,4-DCP 和 2,5-DCP 之间存在统计学显著关联。在基于 i)14 种 EDC(暴露水平)、ii)人口统计学(年龄、性别和地理位置)和 iii)8OHDG(效应)对数据进行聚类后,确定了两个不同的样本聚类。8OHDG 浓度是区分这两个聚类的最关键参数,其次是 OH-EtP。当从数据集删除 8OHDG 时,暴露变量的可预测性按以下顺序增加:OH-EtP>OH-MeP>3,4-DHB>BPA>2,4-DCP>MeP>TCS>EtP>BP1>2,5-DCP。我们的结果表明,OH-EtP、OH-MeP、3,4-DHB、BPA、2,4-DCP、MeP、TCS、EtP、BP1 和 2,5-DCP 的共同暴露与儿童的 DNA 损伤有关。这是第一项报告巴西儿童接触广泛的 EDC 以及数据挖掘方法进一步加强我们对化学共同暴露和效应生物标志物的发现的研究。