Liang Xinxiu, Grill Sarah, Shen Xilin, Williams Paige L, James-Todd Tamarra, Ford Jennifer B, Rexrode Kathryn M, Calafat Antonia M, Chavarro Jorge E, Hauser Russ, Mínguez-Alarcón Lidia
Departments of Nutrition and Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Environ Int. 2025 Aug;202:109652. doi: 10.1016/j.envint.2025.109652. Epub 2025 Jun 29.
Evidence on the association between maternal phenol exposure and inflammation during pregnancy is limited and inconsistent.
To evaluate associations between urinary phenol biomarkers and serum inflammatory cytokines across pregnancy, and to examine whether associations vary by trimesters.
We included 175 pregnant women from the Massachusetts General Hospital Fertility Center and participating in the Environment and Reproductive Health (EARTH) Study (2005-2017), with available data on urinary concentrations of eight phenol biomarkers and serum inflammatory biomarkers, high-sensitivity C-reactive protein (hsCRP) and interleukin-6 (IL-6). Linear regression models were employed to assess the association between individual phenol biomarker concentrations and log-transformed inflammatory cytokine levels, while Bayesian Kernel Machine Regression (BKMR) models were utilized to evaluate phenol biomarker mixtures. Analyses were further stratified by the trimester of sample collection.
Overall, detectable urinary ethylparaben was positively associated with serum hsCRP (β: 0.464; 95 % CI: 0.012, 0.917). In trimester-specific analyses, urinary butylparaben was positively associated with hsCRP (β: 0.533; 95 % CI: 0.006, 1.059) in the first trimester, but negatively associated with IL-6 (β: -0.613; 95 % CI: -1.062, -0.164) in the second trimester. Urinary bisphenol A was inversely associated with hsCRP (β: -0.428; 95 % CI: -0.731, -0.125) in the third trimester.
Our findings suggest that exposure to certain phenols may disrupt inflammatory profiles in pregnancy, with effects varying by trimesters. These novel associations underscore the importance of exposure timing when assessing environmental risk factors for maternal and offspring health outcomes.
关于孕期母亲接触苯酚与炎症之间关联的证据有限且不一致。
评估孕期尿中苯酚生物标志物与血清炎症细胞因子之间的关联,并检验这种关联是否因孕期不同阶段而异。
我们纳入了来自麻省总医院生育中心并参与环境与生殖健康(EARTH)研究(2005 - 2017年)的175名孕妇,她们有关于8种苯酚生物标志物尿浓度以及血清炎症生物标志物、高敏C反应蛋白(hsCRP)和白细胞介素 - 6(IL - 6)的可用数据。采用线性回归模型评估个体苯酚生物标志物浓度与对数转换后的炎症细胞因子水平之间的关联,同时利用贝叶斯核机器回归(BKMR)模型评估苯酚生物标志物混合物。分析进一步按样本采集的孕期阶段进行分层。
总体而言,可检测到的尿中对羟基苯甲酸乙酯与血清hsCRP呈正相关(β:0.464;95%置信区间:0.012,0.917)。在特定孕期分析中,尿中对羟基苯甲酸丁酯在孕早期与hsCRP呈正相关(β:0.533;95%置信区间:0.006,1.059),但在孕中期与IL - 6呈负相关(β: - 0.613;95%置信区间: - 1.062, - 0.164)。尿中双酚A在孕晚期与hsCRP呈负相关(β: - 0.428;95%置信区间: - 0.731, - 0.125)。
我们的研究结果表明,接触某些苯酚可能会扰乱孕期的炎症特征,其影响因孕期阶段而异。这些新的关联强调了在评估环境危险因素对母婴健康结局的影响时,接触时间的重要性。