Department of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, MA, USA; Department of Nutrition, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Ethos Research & Development, Newport KY, USA.
Environ Int. 2020 May;138:105643. doi: 10.1016/j.envint.2020.105643. Epub 2020 Mar 14.
Quinolinic acid (QA), a neuroactive metabolite produced during tryptophan degradation, is implicated in the pathogenesis of several neurological disorders. Phthalates are structurally similar to QA, and exposure to phthalates has demonstrated increased QA production and excretion in rodent studies. We recently showed that very high exposure to dibutyl phthalate was associated with higher concentrations of urinary QA in men. However, no human studies examined the associations between background (low) phthalate exposures and QA.
To examine the associations of urinary concentrations of phthalate metabolites with QA.
Female participants (N = 126) who participated in a prospective cohort study at the Massachusetts General Hospital Fertility Center provided 758 urine samples (273 during pregnancy and 485 during non-pregnancy). Concentrations of 11 phthalate metabolites and QA in urine were measured. We used multivariable linear mixed effect models to estimate the percent change in urinary QA concentrations associated with a doubling (100%) of urinary phthalate metabolite concentration, and evaluated whether there was effect modification by pregnancy status.
Women's mean (standard deviation) age was 34.2 (4.0) years with a body mass index of 23.5 (3.7) kg/m. The women were primarily Caucasian (92%), had at least a college degree (98%), and none were current smokers. Pairwise Spearman correlations between concentrations for phthalate metabolites and QA measured in the same urine samples ranged from 0.36 for MEHP to 0.68 for dibutyl phthalate (DBP) metabolites. In multivariable-adjusted models, the percent change in urinary QA concentrations was significantly higher for each doubling of several urinary phthalate metabolite concentrations. For example, each doubling of DBP metabolites was associated with a 13.7% (95%CI: 10.6, 16.9)% higher QA. Associations between the low molecular weight phthalate metabolites and QA were stronger among samples collected during pregnancy as compared to non-pregnancy samples from the same women.
Urinary concentrations of several phthalate metabolites were positively associated with QA among women. These findings, along with the known neurotoxicity of QA, warrant the need to examine whether QA concentrations may serve as a pathway for the adverse neurodevelopment outcomes found in children's health studies.
喹啉酸(QA)是色氨酸降解过程中产生的一种神经活性代谢物,与多种神经疾病的发病机制有关。邻苯二甲酸酯与 QA 在结构上相似,啮齿动物研究表明,邻苯二甲酸酯暴露会增加 QA 的产生和排泄。我们最近的研究表明,极高水平的二丁基邻苯二甲酸酯暴露与男性尿液中 QA 浓度升高有关。然而,尚无人类研究探讨背景(低水平)邻苯二甲酸酯暴露与 QA 之间的关联。
研究尿液中邻苯二甲酸代谢物浓度与 QA 之间的关系。
参加马萨诸塞州综合医院生育中心前瞻性队列研究的女性参与者(N=126)共提供了 758 份尿液样本(妊娠期间 273 份,非妊娠期间 485 份)。测量尿液中 11 种邻苯二甲酸代谢物和 QA 的浓度。我们使用多变量线性混合效应模型来估计与尿液邻苯二甲酸代谢物浓度翻倍(100%)相关的尿液 QA 浓度的百分比变化,并评估妊娠状态是否存在效应修饰。
女性的平均(标准差)年龄为 34.2(4.0)岁,体重指数为 23.5(3.7)kg/m²。参与者主要为白种人(92%),至少受过大学教育(98%),且无人当前吸烟。在同一样本中测量的邻苯二甲酸代谢物和 QA 的浓度之间的两两 Spearman 相关系数范围为 0.36(MEHP)至 0.68(DBP 代谢物)。在多变量调整模型中,几种尿液邻苯二甲酸代谢物浓度每翻倍一次,尿液 QA 浓度的百分比变化显著升高。例如,DBP 代谢物的每翻倍与 QA 升高 13.7%(95%CI:10.6,16.9)有关。与同一位女性非妊娠样本相比,妊娠样本中低分子量邻苯二甲酸代谢物与 QA 之间的关联更强。
女性尿液中几种邻苯二甲酸代谢物浓度与 QA 呈正相关。这些发现以及 QA 的已知神经毒性表明,有必要研究 QA 浓度是否可能成为儿童健康研究中发现的不良神经发育结果的途径。