Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, GA, USA; Division of Surveillance, Hazard Evaluations and Field Studies, National Institute for Occupational Safety and Health, Cincinnati, OH, USA.
Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, USA.
Environ Int. 2018 Jul;116:214-228. doi: 10.1016/j.envint.2018.04.004. Epub 2018 Apr 23.
Carbon nanotubes and nanofibers (CNT/F) are increasingly used for diverse applications. Although animal studies suggest CNT/F exposure may cause deleterious health effects, human epidemiological studies have typically been small, confined to single workplaces, and limited in exposure assessment.
We conducted an industrywide cross-sectional epidemiological study of 108 workers from 12 U.S. sites to evaluate associations between occupational CNT/F exposure and sputum and blood biomarkers of early effect.
We assessed CNT/F exposure via personal breathing zone, filter-based air sampling to measure background-corrected elemental carbon (EC) (a CNT/F marker) mass and microscopy-based CNT/F structure count concentrations. We measured 36 sputum and 37 blood biomarkers. We used factor analyses with varimax rotation to derive factors among sputum and blood biomarkers separately. We used linear, Tobit, and unconditional logistic regression models to adjust for potential confounders and evaluate associations between CNT/F exposure and individual biomarkers and derived factors.
We derived three sputum and nine blood biomarker factors that explained 78% and 67%, respectively, of the variation. After adjusting for potential confounders, inhalable EC and total inhalable CNT/F structures were associated with the most sputum and blood biomarkers, respectively. Biomarkers associated with at least three CNT/F metrics were 72 kDa type IV collagenase/matrix metalloproteinase-2 (MMP-2), interleukin-18, glutathione peroxidase (GPx), myeloperoxidase, and superoxide dismutase (SOD) in sputum and MMP-2, matrix metalloproteinase-9, metalloproteinase inhibitor 1/tissue inhibitor of metalloproteinases 1, 8-hydroxy-2'-deoxyguanosine, GPx, SOD, endothelin-1, fibrinogen, intercellular adhesion molecule 1, vascular cell adhesion protein 1, and von Willebrand factor in blood, although directions of associations were not always as expected.
Inhalable rather than respirable CNT/F was more consistently associated with fibrosis, inflammation, oxidative stress, and cardiovascular biomarkers.
碳纳米管和纳米纤维(CNT/F)越来越多地用于各种应用。尽管动物研究表明 CNT/F 暴露可能会对健康造成有害影响,但人类流行病学研究通常规模较小,仅限于单个工作场所,并且暴露评估有限。
我们对来自美国 12 个地点的 108 名工人进行了全行业的横断面流行病学研究,以评估职业 CNT/F 暴露与痰液和血液早期效应生物标志物之间的关联。
我们通过个人呼吸区评估 CNT/F 暴露情况,通过基于过滤器的空气采样来测量背景校正后的元素碳(EC)(CNT/F 标志物)质量和基于显微镜的 CNT/F 结构计数浓度。我们测量了 36 份痰液和 37 份血液生物标志物。我们使用具有方差最大旋转的因子分析分别对痰液和血液生物标志物进行因子分析。我们使用线性、Tobit 和非条件逻辑回归模型,调整潜在混杂因素,并评估 CNT/F 暴露与个体生物标志物和衍生因子之间的关联。
我们得出了三个与痰液和九个与血液生物标志物分别解释 78%和 67%变化的因子。在调整潜在混杂因素后,可吸入 EC 和总可吸入 CNT/F 结构分别与最多的痰液和血液生物标志物相关。与至少三个 CNT/F 指标相关的生物标志物分别为痰液中的 72kDa 型 IV 胶原酶/基质金属蛋白酶-2(MMP-2)、白细胞介素-18、谷胱甘肽过氧化物酶(GPx)、髓过氧化物酶和超氧化物歧化酶(SOD),以及血液中的 MMP-2、基质金属蛋白酶-9、金属蛋白酶抑制剂 1/组织金属蛋白酶抑制剂 1、8-羟基-2'-脱氧鸟苷、GPx、SOD、内皮素-1、纤维蛋白原、细胞间黏附分子 1、血管细胞黏附蛋白 1 和血管性血友病因子,尽管关联方向并不总是如预期的那样。
可吸入而非可呼吸 CNT/F 与纤维化、炎症、氧化应激和心血管生物标志物的相关性更为一致。