Department of Environmental Health and Engineering, Johns Hopkins University Bloomberg School of Public Health, 615 N. Wolfe Street, Room W7513A, Baltimore, MD, 21205, USA.
Nicholas School of the Environment, Duke University, Durham, NC, USA.
Environ Health. 2020 May 24;19(1):55. doi: 10.1186/s12940-020-00610-0.
Organophosphate esters (OPEs) are synthetic chemicals used as flame retardants and plasticizers in a variety of goods. Despite ubiquitous human exposures and laboratory evidence that prenatal OPE exposures may disrupt offspring metabolism, perinatal studies of OPE health effects are limited. The objectives of this study were to: 1) Determine predictors and reproducibility of urinary OPE biomarker concentrations during pregnancy, and 2) Estimate the relation of prenatal OPE exposures with birth outcomes and cord blood adipokine and insulin concentrations.
We analyzed five OPE metabolites in urine samples collected at up to three visits during pregnancy from 90 women enrolled in the ORigins of Child Health And Resilience in Development (ORCHARD) pregnancy cohort in Baltimore, MD from 2017 to 2019. To quantify the variability of metabolite concentrations during pregnancy, we calculated intraclass correlation coefficients (ICCs) for each metabolite using mixed effects regression models. Using self-reported questionnaire data collected during gestation, we assessed possible sociodemographic and environmental/behavioral predictors of each OPE metabolite using generalized estimating equations to account for repeated exposure measures. We ascertained birth outcomes of 76 offspring from medical records, including weight-for-gestational age, length, ponderal index, and gestational age. In a subset of 37 infants, we measured cord blood concentrations of leptin, adiponectin, and insulin. To account for repeated exposure measures, we used linear structural equation models to assess the relations of standard deviation (SD) increases in prenatal OPE metabolite factor scores with continuous birth outcomes and cord blood biomarker concentrations.
ICCs ranged from 0.09 for isopropylphenyl-phenyl phosphate (ip-PPP) to 0.59 for bis(1,3-dichloro-2-propyl) phosphate (BDCIPP). We observed little consistency in environmental or behavioral predictors of OPE exposures, although concentrations were generally lower for samples collected in the afternoon compared to morning and winter compared to other seasons. In adjusted analyses, a SD increase in BDCIPP concentration was associated with a 0.06 g/cm (95% CI: 0.00, 0.12) greater ponderal index. A SD increase in BDCIPP was associated with a 0.37 (95% CI: - 0.62, - 0.13) SD lower insulin concentration and 0.24 (95% CI: - 0.39, - 0.08) SD lower leptin concentration. Other OPEs were not associated with infant outcomes.
These findings suggest some OPEs may be metabolic disruptors warranting investigation in larger studies.
有机磷酸酯 (OPE) 是一种合成化学品,用作各种商品的阻燃剂和增塑剂。尽管人类普遍接触 OPE 并在实验室中证明产前 OPE 暴露可能会破坏后代的新陈代谢,但关于 OPE 健康影响的围产期研究有限。本研究的目的是:1)确定妊娠期间尿液中 OPE 生物标志物浓度的预测因素和可重复性,以及 2)估计产前 OPE 暴露与出生结局以及脐血中脂肪因子和胰岛素浓度的关系。
我们分析了 90 名参加巴尔的摩 ORigins of Child Health And Resilience in Development (ORCHARD) 妊娠队列的女性在 2017 年至 2019 年期间妊娠期间最多三次就诊时收集的尿液样本中的五种 OPE 代谢物。为了量化妊娠期间代谢物浓度的变异性,我们使用混合效应回归模型为每个代谢物计算了组内相关系数 (ICC)。使用在妊娠期间收集的自我报告问卷数据,我们使用广义估计方程评估了每个 OPE 代谢物的可能社会人口统计学和环境/行为预测因素,以考虑重复的暴露测量。我们从医疗记录中确定了 76 名后代的出生结局,包括体重与胎龄比、长度、体重指数和胎龄。在 37 名婴儿的亚组中,我们测量了脐血中瘦素、脂联素和胰岛素的浓度。为了考虑重复的暴露测量,我们使用线性结构方程模型评估了产前 OPE 代谢物因子得分的标准差 (SD) 增加与连续出生结局和脐血生物标志物浓度的关系。
ICCs 范围从异丙基苯基-苯基磷酸酯 (ip-PPP) 的 0.09 到双-(1,3-二氯-2-丙基)磷酸酯 (BDCIPP) 的 0.59。我们观察到 OPE 暴露的环境或行为预测因素几乎没有一致性,尽管与早上和冬季相比,下午采集的样本中 OPE 浓度通常较低。在调整分析中,BDCIPP 浓度的 SD 增加与体重指数增加 0.06 g/cm(95%CI:0.00,0.12)相关。BDCIPP 的 SD 增加与胰岛素浓度降低 0.37(95%CI:-0.62,-0.13)和瘦素浓度降低 0.24(95%CI:-0.39,-0.08)相关。其他 OPE 与婴儿结局无关。
这些发现表明,一些 OPE 可能是代谢干扰物,值得在更大的研究中进一步研究。