尿液中挥发性有机化合物代谢物与美国儿童和青少年肺功能降低有关。

Toxics Pub Date : 2024-04-16 DOI:10.3390/toxics12040289
A. Mendy, Sara Burcham, A. Merianos, T. Mersha, K. Yolton, Aimin Chen, E. M. Mahabee-gittens
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摘要

(1) 背景:挥发性有机化合物(VOC)是通过吸入吸收的室内污染物。几种挥发性有机化合物与儿童和青少年肺功能的关系尚不清楚。(2) 方法:我们对 2011-2012 年全国健康与营养调查中的 505 名 6-17 岁参与者进行了分析。采用多元线性回归模型来估计挥发性有机化合物代谢物与肺活量测定结果之间的关系,并对协变量进行调整。(3)结果:尿液中二甲苯、丙烯酰胺、丙烯醛、1,3-丁二烯、氰化物、甲苯、1-溴丙烷、丙烯腈、环氧丙烷、苯乙烯、乙苯和巴豆醛代谢物的检出率均≥64.5%。丙烯酰胺(β:-7.95,95% CI:-13.69,-2.21)和苯乙烯(β:-6.33,95% CI:-11.60,-1.07)代谢物水平较高的参与者 1 秒钟用力呼气容积(FEV1)预测百分比较低,而环氧丙烷代谢物水平较高的儿童 FEV1 与用力呼吸容量(FVC)比值百分比较低(β:-2.05,95% CI:-3.49,-0.61)。只有在超重/肥胖参与者中,巴豆醛代谢物水平越高,FEV1 预测值百分比越低(β:-15.42,95% CI:-26.76,-4.08)(平特作用<0.001);只有在血清可替宁大于 1 ng/mL 的参与者中,1-溴丙烷代谢物水平越高,FEV1 预测值百分比越低(β:-6.26,95% CI:-9.69,-2.82)(平特作用<0.001)。(4)结论:我们发现丙烯酰胺、环氧丙烷、苯乙烯、1-溴丙烷和巴豆醛的代谢物与儿童和青少年较低的肺功能有新的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urinary Volatile Organic Compound Metabolites Are Associated with Reduced Lung Function in U.S. Children and Adolescents.
(1) Background: Volatile organic compounds (VOCs) are indoor pollutants absorbed by inhalation. The association of several VOCs with lung function in children and adolescents is unknown. (2) Methods: We analyzed 505 participants, 6-17-year-olds from the 2011-2012 National Health and Nutrition Examination Survey. Multiple linear regression models were fitted to estimate the associations of VOC metabolites with spirometry outcomes adjusting for covariates. (3) Results: Urinary metabolites of xylene, acrylamide, acrolein, 1,3-butadiene, cyanide, toluene, 1-bromopropane, acrylonitrile, propylene oxide, styrene, ethylbenzene, and crotonaldehyde were all detected in ≥64.5% of participants. Forced expiratory volume in 1 s (FEV1) % predicted was lower in participants with higher levels of metabolites of acrylamide (β: -7.95, 95% CI: -13.69, -2.21) and styrene (β: -6.33, 95% CI: -11.60, -1.07), whereas the FEV1 to forced vital capacity (FVC) ratio % was lower in children with higher propylene oxide metabolite levels (β: -2.05, 95% CI: -3.49, -0.61). FEV1 % predicted was lower with higher crotonaldehyde metabolite levels only in overweight/obese participants (β: -15.42, 95% CI: -26.76, -4.08) (Pinteraction < 0.001) and with higher 1-bromopropane metabolite levels only in those with serum cotinine > 1 ng/mL (β: -6.26, 95% CI: -9.69, -2.82) (Pinteraction < 0.001). (4) Conclusions: We found novel associations of metabolites for acrylamide, propylene oxide, styrene, 1-bromopropane and crotonaldehyde with lower lung function in children and adolescents.
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