Shao Wentao, Gong Pan, Wang Qihan, Ding Fan, Shen Weiyi, Zhang Hongchao, Huang Anhua, Liu Chengyu
School of Instrument Science and Engineering, Southeast University, Nanjing, China.
Center of Gallstone Disease, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Front Public Health. 2025 Jan 17;12:1437519. doi: 10.3389/fpubh.2024.1437519. eCollection 2024.
Volatile organic compounds (VOCs) are pervasive environmental pollutants known to impact human health, but their role in liver steatosis or fibrosis is not fully understood. This study investigates the association of urinary VOC mixtures with the risk of liver steatosis and fibrosis in U.S. adult population.
Data of 1854 adults from the National Health and Nutrition Examination Survey (NHANES) from 2017.01 to 2020.03 were collected. Vibration Controlled Transient Elastography (VCTE) assessed hepatic steatosis and liver fibrosis via the controlled attenuation parameter (CAP) and liver stiffness measurement (LSM), respectively. The study examined the relationship between urinary exposure biomarkers for 20 VOCs and liver health outcomes using multivariate logistic regression and Bayesian Kernel Machine Regression (BKMR) to evaluate the effects of both individual and mixed VOC exposures.
Multivariate logistic regression analysis revealed that exposure biomarkers for acrolein and crotonaldehyde were positively associated with hepatic steatosis. Conversely, biomarkers for styrene, ethylbenzene, and propylene oxide were negatively associated with hepatic steatosis. Furthermore, biomarkers for 1,3-butadiene and xylene were positively associated with liver fibrosis, while ethylbenzene was negatively associated with this condition. BKMR analysis identified a significant positive joint effect of VOC biomarkers on CAP. Notably, when other VOC-EBs were held at median levels, biomarkers for acrolein and 1,3-butadiene exhibited linear correlations with Ln CAP and hepatic Ln LSM, respectively.
The study highlights the potential hepatotoxic effects of VOC mixtures, particularly noting the roles of acrolein and 1,3-butadiene in exacerbating liver steatosis and fibrosis. These findings advocate for further research to explore the mechanistic pathways and conduct longitudinal studies to establish causality and enhance understanding of VOCs' impact on liver health.
挥发性有机化合物(VOCs)是普遍存在的环境污染物,已知会影响人类健康,但其在肝脂肪变性或肝纤维化中的作用尚未完全明确。本研究调查美国成年人群尿中VOC混合物与肝脂肪变性和肝纤维化风险之间的关联。
收集了2017年1月至2020年3月期间美国国家健康与营养检查调查(NHANES)中1854名成年人的数据。振动控制瞬时弹性成像(VCTE)分别通过控制衰减参数(CAP)和肝脏硬度测量(LSM)评估肝脂肪变性和肝纤维化。本研究使用多变量逻辑回归和贝叶斯核机器回归(BKMR)来评估个体和混合VOC暴露的影响,研究了20种VOC的尿暴露生物标志物与肝脏健康结果之间的关系。
多变量逻辑回归分析显示,丙烯醛和巴豆醛的暴露生物标志物与肝脂肪变性呈正相关。相反,苯乙烯、乙苯和环氧丙烷的生物标志物与肝脂肪变性呈负相关。此外,1,3 - 丁二烯和二甲苯的生物标志物与肝纤维化呈正相关,而乙苯与这种情况呈负相关。BKMR分析确定了VOC生物标志物对CAP有显著的正向联合效应。值得注意的是,当其他VOC - EB处于中位数水平时,丙烯醛和1,3 - 丁二烯的生物标志物分别与Ln CAP和肝脏Ln LSM呈线性相关。
该研究突出了VOC混合物潜在的肝毒性作用,特别指出了丙烯醛和1,3 - 丁二烯在加重肝脂肪变性和肝纤维化中的作用。这些发现倡导进一步研究以探索作用机制途径,并进行纵向研究以确定因果关系,加深对VOCs对肝脏健康影响的理解。