School of Public Health, Qingdao University, Qingdao, China.
Key Laboratory of Chemical Safety and Health, National Institute for Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing, China.
Environ Int. 2021 Feb;147:106341. doi: 10.1016/j.envint.2020.106341. Epub 2020 Dec 29.
Oxidative stress has been suggested to be one of the key drivers of health impact of particulate matter (PM). More studies on the oxidative potential of PM alone, but fewer studies have comprehensively evaluated the effects of external and internal exposure to PM compositions on oxidative stress in population.
To comprehensively investigate the exposure-response relationship between PM and its main compositions with oxidative stress indicators.
We conducted a cross-sectional study including 768 participants exposed to particulates. Environmental levels of fine particulate matter (PM), polycyclic aromatic hydrocarbons (PAHs) and metals in PM were measured, and urinary levels of PAHs metabolites and metals were measured as internal dose, respectively. Multivariable linear regression models were used to analyze the correlations of PM exposure and urinary levels of 8-hydroxy-2́'-deoxyguanosine (8-OHdG), and 8-iso-prostaglandin-F2α (8-iso-PGF2α) and malondialdehyde (MDA).
The concentration of both PM and total PAHs was significantly correlated with increased urinary 8-OHdG, 8-iso-PGF2α and MDA levels (all p < 0.05). The levels of 4 essential metals all showed significant exposure-response increase in urinary 8-OHdG in both current and non-current smokers (all p < 0.05); ambient selenium, cobalt and zinc were found to be significantly correlated with urinary 8-iso-PGF2α (p = 0.002, 0.003, 0.01, respectively); only selenium and cobalt were significantly correlated with urinary MDA (p < 0.001, 0.01, respectively). Furthermore, we found each one-unit increase in urinary total OH-PAHs generated a 0.32 increase in urinary 8-OHdG, a 0.22 increase in urinary 8-iso-PGF2α and a 0.19 increase in urinary MDA (all p < 0.001). Furthermore, it was found that the level of 12 urinary metals all showed significant and positive correlations with three oxidative stress biomarkers in all subjects (all p < 0.001).
Our systematic molecular epidemiological study showed that particulate matter components could induce increased oxidative stress on DNA and lipid. It may be more important to monitor and control the harmful compositions in PM rather than overall particulate mass.
氧化应激被认为是颗粒物(PM)对健康影响的关键驱动因素之一。更多的研究关注 PM 的氧化潜能,但较少的研究综合评估了 PM 成分的外暴露和内暴露对人群氧化应激的影响。
全面研究 PM 及其主要成分与氧化应激指标之间的暴露-反应关系。
我们进行了一项横断面研究,纳入了 768 名暴露于颗粒物的参与者。测量了细颗粒物(PM)、多环芳烃(PAHs)和 PM 中金属的环境水平,分别测量了尿液中 PAHs 代谢物和金属的内剂量。采用多变量线性回归模型分析 PM 暴露与尿液中 8-羟基-2'-脱氧鸟苷(8-OHdG)、8-异前列腺素 F2α(8-iso-PGF2α)和丙二醛(MDA)水平的相关性。
PM 浓度和总 PAHs 浓度均与尿液中 8-OHdG、8-iso-PGF2α 和 MDA 水平升高显著相关(均 p<0.05)。在当前吸烟者和非当前吸烟者中,4 种必需金属的水平均与尿液中 8-OHdG 呈显著的暴露-反应性增加(均 p<0.05);环境硒、钴和锌与尿液中 8-iso-PGF2α 显著相关(p=0.002、0.003、0.01);仅硒和钴与尿液 MDA 显著相关(p<0.001、0.01)。此外,我们发现尿液中总 OH-PAHs 每增加一个单位,尿液 8-OHdG 增加 0.32,尿液 8-iso-PGF2α 增加 0.22,尿液 MDA 增加 0.19(均 p<0.001)。此外,在所有受试者中,12 种尿液金属的水平均与三种氧化应激生物标志物呈显著正相关(均 p<0.001)。
本系统的分子流行病学研究表明,颗粒物成分可引起 DNA 和脂质氧化应激增加。与整体颗粒物质量相比,监测和控制 PM 中的有害成分可能更为重要。