Gómez-Olarte Sergio, Röder Stefan, Rolle-Kampczyk Ulrike, Sack Ulrich, von Bergen Martin, Borte Michael, Zenclussen Ana C, Herberth Gunda
Department of Environmental Immunology, Helmholtz Centre for Environmental Research - UFZ, Leipzig, Germany.
Department of Environmental Immunology, Helmholtz Centre for Environmental Research - UFZ, Leipzig, Germany.
Environ Res. 2025 Aug 1;278:121667. doi: 10.1016/j.envres.2025.121667. Epub 2025 Apr 22.
We investigated whether maternal exposure to phthalate and bisphenol A (BPA) mixtures is associated with eczema in children, as most studies have only addressed single chemical exposures.
Nine phthalate metabolites and BPA were quantified in urine at gestational weeks 34-36 (n = 540) and total, inhalant, and food allergen-specific immunoglobulin (Ig)E levels (sx1, and fx5) were measured in serum from 4-year-old children of the LiNA cohort (n = 219). The association of prenatal exposure to phthalates and BPA, both single and mixed, with eczema and IgE was assessed in children stratified by atopy status. Three independent statistical models adjusted for covariates were used: logistic regression -also in the sex-stratified analysis-, weighted quantile sum (WQS) regression, and Bayesian kernel machine regression (BKMR). Moreover, an in silico toxicogenomic analysis was conducted to explore putative underlying mechanisms.
The adjusted logistic regression showed that monobenzyl phthalate (MBzP; OR = 2.64, 95 % CI: 1.29-6.4) and the sum of di-2-ethylhexyl phthalate metabolites (2.09, 1.1-4.32) were significantly associated with eczema exclusively in atopic boys. The BKMR suggested a positive trend between chemical exposure and IgE values in the atopic subgroup. In the WQS model, the mixture' positive effect on eczema among atopic children was significant (1.90, 1.80-2.01) with MBzP (65.9 %), monoethyl phthalate (13.3 %), and BPA (10.9 %) being the main contributors, which jointly modulate antibody-mediated immunity and inflammation gene pathways in the toxicogenomic profiling.
Maternal exposure to mixtures of phthalates and BPA differentially impacts eczema risk among atopy-stratified children. The in silico chemical-gene interaction analysis in atopic children identified genes involved in immune cell activation and Ig production. Compared to non-atopic children, individual phthalates were significantly associated with eczema in atopic boys, suggesting that chemicals may have a larger effect size in predisposed populations.
我们调查了母亲接触邻苯二甲酸盐和双酚A(BPA)混合物是否与儿童湿疹有关,因为大多数研究仅涉及单一化学物质暴露。
在妊娠34 - 36周时对540名孕妇的尿液中的九种邻苯二甲酸酯代谢物和双酚A进行定量分析,并对LiNA队列中219名4岁儿童的血清中的总免疫球蛋白、吸入性和食物过敏原特异性免疫球蛋白(Ig)E水平(sx1和fx5)进行测量。在按特应性状态分层的儿童中评估产前接触邻苯二甲酸盐和双酚A(单一和混合接触)与湿疹和IgE的关联。使用了三种针对协变量进行调整的独立统计模型:逻辑回归(在按性别分层分析中也使用)、加权分位数和(WQS)回归以及贝叶斯核机器回归(BKMR)。此外,还进行了计算机毒理基因组学分析以探索潜在的机制。
调整后的逻辑回归显示,仅在特应性男孩中,邻苯二甲酸单苄酯(MBzP;OR = 2.64,95% CI:1.29 - 6.4)和邻苯二甲酸二(2 - 乙基己基)酯代谢物总和(2.09,1.1 - 4.32)与湿疹显著相关。BKMR表明在特应性子组中化学物质暴露与IgE值之间呈正趋势。在WQS模型中,混合物对特应性儿童湿疹的积极影响显著(1.90,1.80 - 2.01),其中MBzP(65.9%)、邻苯二甲酸单乙酯(13.3%)和双酚A(10.9%)是主要贡献者,它们在毒理基因组分析中共同调节抗体介导的免疫和炎症基因途径。
母亲接触邻苯二甲酸盐和双酚A混合物对按特应性分层的儿童湿疹风险有不同影响。对特应性儿童的计算机化学 - 基因相互作用分析确定了参与免疫细胞激活和Ig产生的基因。与非特应性儿童相比,个别邻苯二甲酸盐在特应性男孩中与湿疹显著相关,这表明化学物质在易感人群中可能具有更大的效应量。