Hokkaido University Center for Environmental and Health Sciences, Kita 12, Nishi 7, Kita-ku, Sapporo 060-0812, Japan.
Toxicological Center, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium.
Environ Int. 2019 Oct;131:105003. doi: 10.1016/j.envint.2019.105003. Epub 2019 Jul 13.
Organophosphate flame retardants (PFRs) are used as additives in plastics and other applications such as curtains and carpets as a replacement for brominated flame retardants. As such, exposure to PFR mixtures is widespread, with children being more vulnerable than adults to associated health risks such as allergies and inflammation. Oxidative stress is thought to be able to modulate the development of childhood airway inflammation and atopic dermatitis. To evaluate these associations, the present study investigated the relationship between urinary PFR metabolites, their mixtures and urinary oxidative stress biomarkers in children as part of the Hokkaido Study on Environment and Children's Health. The levels of the oxidative stress biomarkers, such as 8-hydroxy-2'-deoxyguanosine (8-OHdG), hexanoyl-lysine (HEL), and 4-hydroxynonenal (HNE), and of 14 PFR metabolites were measured in morning spot urine samples of 7-year-old children (n = 400). Associations between PFR metabolites or PFR metabolite mixtures and oxidative stress biomarkers were examined by multiple regression analysis and weighted quantile sum regression analysis, respectively. We found that the non-chlorinated PFR metabolites, 2-ethylhexyl phenyl phosphate (EHPHP), bis(2-butoxyethyl) phosphate (BBOEP), and diphenyl phosphate (DPHP) were associated with increased levels of oxidative stress biomarkers. Furthermore, the PFR metabolite mixture was associated with increased levels of HEL and HNE, but not 8-OHdG. The combination of elevated top 2 PFR metabolites was not associated with higher urinary oxidative stress marker levels. This is the first study to report associations between urinary PFR metabolites and oxidative stress biomarkers among children.
有机磷阻燃剂(PFRs)作为添加剂用于塑料和其他应用,如窗帘和地毯,以替代溴化阻燃剂。因此,PFR 混合物的暴露很普遍,儿童比成年人更容易受到过敏和炎症等相关健康风险的影响。氧化应激被认为能够调节儿童气道炎症和特应性皮炎的发展。为了评估这些关联,本研究在北海道环境与儿童健康研究中,调查了儿童尿液中 PFR 代谢物及其混合物与尿液氧化应激生物标志物之间的关系。在 7 岁儿童的晨尿样本(n=400)中测量了氧化应激生物标志物的水平,如 8-羟基-2'-脱氧鸟苷(8-OHdG)、己酰赖氨酸(HEL)和 4-羟基壬烯醛(HNE),以及 14 种 PFR 代谢物。通过多元回归分析和加权分位数和回归分析分别检查了 PFR 代谢物或 PFR 代谢物混合物与氧化应激生物标志物之间的关系。我们发现,非氯化 PFR 代谢物 2-乙基己基苯基磷酸酯(EHPHP)、双(2-丁氧基乙基)磷酸酯(BBOEP)和磷酸二苯酯(DPHP)与氧化应激生物标志物水平升高有关。此外,PFR 代谢物混合物与 HEL 和 HNE 水平升高有关,但与 8-OHdG 无关。升高的前 2 种 PFR 代谢物的组合与更高的尿液氧化应激标志物水平无关。这是第一项报告儿童尿液中 PFR 代谢物与氧化应激生物标志物之间关联的研究。