Department of Epidemiology, University of California, Los Angeles, CA, 90095, USA.
Department of Environmental Health Sciences, University of California, Los Angeles, CA, 90095, USA.
Environ Health. 2024 Aug 13;23(1):68. doi: 10.1186/s12940-024-01107-w.
Polycyclic aromatic hydrocarbons (PAHs) have been linked to adverse birth outcomes that have been reported to be induced by oxidative stress, but few epidemiological studies to date have evaluated associations between urinary PAH metabolites and oxidative stress biomarkers in pregnancy and identified critical periods for these outcomes and PAH exposures in pregnancy.
A cohort of pregnant women was recruited early in pregnancy from antenatal clinics at the University of California Los Angeles during 2016-2019. We collected urine samples up to three times during pregnancy in a total of 159 women enrolled in the cohort. A total of 7 PAH metabolites and 2 oxidative stress biomarkers [malondialdehyde (MDA), 8-hydroxy-2'-deoxyguanosine (8-OHdG)] were measured in all available urine samples. Using multiple linear regression models, we estimated the percentage change (%) and 95% confidence interval (CI) in 8-OHdG and MDA measured at each sample collection time per doubling of PAH metabolite concentrations. Furthermore, we used linear mixed models with a random intercept for participant to estimate the associations between PAH metabolite and oxidative stress biomarker concentrations across multiple time points in pregnancy.
Most PAH metabolites were positively associated with both urinary oxidative stress biomarkers, MDA and 8-OHdG, with stronger associations in early and late pregnancy. A doubling of each urinary PAH metabolite concentration increased MDA concentrations by 5.8-41.1% and 8-OHdG concentrations by 13.8-49.7%. Linear mixed model results were consistent with those from linear regression models for each gestational sampling period.
Urinary PAH metabolites are associated with increases in oxidative stress biomarkers during pregnancy, especially in early and late pregnancy.
多环芳烃(PAHs)与不良出生结局有关,这些不良结局据报道是由氧化应激引起的,但迄今为止,很少有流行病学研究评估妊娠期间尿液中 PAH 代谢物与氧化应激生物标志物之间的关系,并确定这些结果和妊娠期间 PAH 暴露的关键时期。
本研究于 2016 年至 2019 年期间在加利福尼亚大学洛杉矶分校的产前诊所招募了一批妊娠早期的孕妇。我们在总共 159 名入组队列的孕妇中,在妊娠期间最多采集了 3 次尿液样本。在所有可用的尿液样本中,共测量了 7 种 PAH 代谢物和 2 种氧化应激生物标志物[丙二醛(MDA)、8-羟基-2'-脱氧鸟苷(8-OHdG)]。使用多元线性回归模型,我们估计了每个样本采集时间点 MDA 和 8-OHdG 测量值的变化百分比(%)和 95%置信区间(CI),每个 PAH 代谢物浓度加倍。此外,我们使用线性混合模型,为参与者设置随机截距,以估计妊娠期间多个时间点 PAH 代谢物和氧化应激生物标志物浓度之间的关联。
大多数 PAH 代谢物与尿液中两种氧化应激生物标志物 MDA 和 8-OHdG 均呈正相关,在妊娠早期和晚期的相关性更强。每种尿液 PAH 代谢物浓度加倍,MDA 浓度增加 5.8-41.1%,8-OHdG 浓度增加 13.8-49.7%。线性混合模型结果与每个妊娠采样期的线性回归模型结果一致。
妊娠期间,尿液中 PAH 代谢物与氧化应激生物标志物的增加有关,尤其是在妊娠早期和晚期。