Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University, Beijing Municipal Key Laboratory of Clinical Epidemiology, Beijing, 100069, China.
Department of Occupational and Environmental Health Sciences, Peking University School of Public Health, Beijing, 100191, China.
Environ Pollut. 2022 May 15;301:119026. doi: 10.1016/j.envpol.2022.119026. Epub 2022 Feb 18.
The short-term alteration of peripheral cytokines may be an early adverse health effect of PM exposure and may be further associated with cardiovascular disease. We conducted a randomized, double-blind crossover trial using true or sham air filtration among 54 healthy college students in Beijing to investigate the potential benefits of short-term indoor air filtration and the adverse health effects of time-weighted personal PM exposure through inflammatory cytokines. The participants randomly received true or sham air filtration intervention for a week, and the treatment was changed after a two-week washout period. Peripheral blood samples were collected after each intervention period to measure 38 inflammatory cytokines. A linear mixed-effects model was applied to estimate the impacts of air purification or a 10 μg/m PM exposure increase on cytokines. Lag effects of PM exposure were analyzed using single-day and moving average lag models. Air filtration reduced indoor and time-weighted average personal PM concentrations by 69.0% (from 33.6 to 10.4 μg/m) and 40.3% (from 40.6 to 24.3 μg/m), respectively. We observed a significant association of PM exposure with growth-regulated alpha protein (GRO-α) of -11.3% (95%CI: 17.0%, -5.4%). In the lag models, significant associations between personal PM exposure and interleukin-1 receptor antagonist (IL-1Ra), monocyte chemotactic protein (MCP-1), and eotaxin were obtained at lag0, while associations with cytokines including vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), fibroblast growth factor-2 (FGF-2), granulocyte colony-stimulating factor (G-CSF), macrophage inflammatory protein-1β (MIP-1β), IL-4, tumor necrosis factor-α (TNF-α), and interferon-γ (IFN-γ) were noted at relatively long lagged exposure windows (lag5-lag6). No significant alteration in cytokines was observed under true air filtration intervention. Our study indicates the effectiveness of air filtration on indoor PM reduction. PM exposure may decrease GRO-α levels and change different cytokine levels time-varyingly. Further study is still needed to explore the mechanisms of PM exposure on the inflammatory response.
短期外周细胞因子的改变可能是 PM 暴露的早期不良健康影响,并且可能与心血管疾病进一步相关。我们在北京的 54 名健康大学生中进行了一项随机、双盲交叉试验,使用真实或虚假空气过滤来研究短期室内空气过滤的潜在益处和通过炎症细胞因子的个人 PM 暴露的时间加权的不良健康影响。参与者随机接受真实或虚假空气过滤干预一周,在两周洗脱期后改变治疗。在每个干预期后收集外周血样以测量 38 种炎症细胞因子。应用线性混合效应模型来估计空气净化或 PM 暴露增加 10μg/m 对细胞因子的影响。使用单日和移动平均滞后模型分析 PM 暴露的滞后效应。空气过滤使室内和时间加权平均个人 PM 浓度分别降低了 69.0%(从 33.6μg/m 降至 10.4μg/m)和 40.3%(从 40.6μg/m 降至 24.3μg/m)。我们观察到 PM 暴露与生长调节α蛋白(GRO-α)呈负相关,相关系数为-11.3%(95%CI:17.0%,-5.4%)。在滞后模型中,在滞后 0 时观察到个人 PM 暴露与白细胞介素 1 受体拮抗剂(IL-1Ra)、单核细胞趋化蛋白 1(MCP-1)和嗜酸性粒细胞趋化因子之间存在显著关联,而与血管内皮生长因子(VEGF)、表皮生长因子(EGF)、成纤维细胞生长因子-2(FGF-2)、粒细胞集落刺激因子(G-CSF)、巨噬细胞炎症蛋白 1β(MIP-1β)、IL-4、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)等细胞因子的关联则在相对较长的滞后暴露窗口(滞后 5-6)中观察到。在真实空气过滤干预下,细胞因子没有明显变化。我们的研究表明空气过滤对室内 PM 减少的有效性。PM 暴露可能会降低 GRO-α 水平,并随时间变化改变不同的细胞因子水平。需要进一步研究来探索 PM 暴露对炎症反应的机制。