Epidemiology Branch, National Institute of Environmental Health Sciences, Durham, NC, USA.
School of Public Health, University of Nevada Reno, Reno, NV, USA.
Environ Res. 2024 Dec 1;262(Pt 2):119910. doi: 10.1016/j.envres.2024.119910. Epub 2024 Sep 2.
Organophosphate esters (OPEs), flame retardants and plasticizers found widely in consumer products, may impact vascularization processes in pregnancy. Yet, the association between maternal exposure to OPEs and both preeclampsia and blood pressure during pregnancy remains understudied.
Within the LIFECODES Fetal Growth Study (N = 900), we quantified 8 OPE metabolites from maternal urine collected at up to 3 time points during pregnancy and created within-subject geometric means. Outcomes included diagnosis of preeclampsia and longitudinal systolic (SBP) and diastolic (DBP) blood pressure measurements (mean = 14 per participant). Cox proportional hazards models were used to estimate associations between OPE metabolites and preeclampsia. Associations between average OPE metabolite concentrations and repeated blood pressure measurements were estimated using generalized estimating equations.
Five OPE metabolites were detected in at least 60% of samples; 3 metabolites detected less frequently (5-39%) were examined in an exploratory analysis as ever vs. never detectable in pregnancy. There were 46 cases of preeclampsia in our study population. Associations between OPE metabolites and preeclampsia were null. We noted several divergent associations between OPE metabolites and longitudinal blood pressure measurements. An interquartile range (IQR) difference in average bis(2-chloroethyl) phosphate concentrations was associated with a decrease in SBP (-0.81 mmHg, 95% confidence interval [CI]: -1.62, 0.00), and, conversely, bis(1-chloro-2-propyl) phosphate was associated with a slight increase in SBP (0.94 mmHg, 95% CI: 0.28, 1.61). We also noted a decrease in SBP in association with several metabolites with low detection frequency.
We observed null associations between OPE metabolites and preeclampsia, but some positive and some inverse associations with blood pressure in pregnancy. While our study was well-designed to assess associations with blood pressure, future studies with a larger number of preeclampsia cases may be better poised to investigate the association between OPE metabolites and phenotypes of this heterogenous hypertensive disorder of pregnancy.
在消费产品中广泛发现的有机磷酸酯 (OPEs)、阻燃剂和增塑剂,可能会影响妊娠期间的血管生成过程。然而,母体暴露于 OPEs 与子痫前期和妊娠期间血压之间的关联仍研究不足。
在 LIFECODES 胎儿生长研究(N=900)中,我们定量检测了 8 种母体尿液中的 OPE 代谢物,这些代谢物是在妊娠期间最多 3 个时间点采集的,并创建了个体内几何平均值。结局包括子痫前期的诊断和纵向收缩压 (SBP) 和舒张压 (DBP) 血压测量(平均每个参与者 14 次)。使用 Cox 比例风险模型估计 OPE 代谢物与子痫前期之间的关联。使用广义估计方程估计平均 OPE 代谢物浓度与重复血压测量之间的关联。
在至少 60%的样本中检测到 5 种 OPE 代谢物;在探索性分析中,检测频率较低(5-39%)的 3 种代谢物被检查为妊娠期间是否可检测到。我们的研究人群中共有 46 例子痫前期病例。OPE 代谢物与子痫前期之间无关联。我们注意到 OPE 代谢物与纵向血压测量之间存在一些不一致的关联。平均双(2-氯乙基)磷酸浓度的四分位距 (IQR) 差异与 SBP 下降相关 (-0.81mmHg,95%置信区间 [CI]:-1.62,0.00),相反,双(1-氯-2-丙基)磷酸与 SBP 略有升高相关 (0.94mmHg,95%CI:0.28,1.61)。我们还注意到与一些低检测频率的代谢物相关的 SBP 下降。
我们观察到 OPE 代谢物与子痫前期之间无关联,但与妊娠期间的血压存在一些正相关和一些负相关。虽然我们的研究设计很好地评估了与血压的关联,但未来具有更多子痫前期病例的研究可能更有能力研究 OPE 代谢物与这种异质性妊娠高血压疾病表型之间的关联。