Division of Clinical Pharmacology and Experimental Therapeutics, Medical Service, Departments of Medicine and Biopharmaceutical Sciences, University of California, San Francisco, California.
Center for Tobacco Control Research and Education, University of California, San Francisco, California.
Cancer Epidemiol Biomarkers Prev. 2018 Mar;27(3):254-261. doi: 10.1158/1055-9965.EPI-17-0671. Epub 2018 Feb 23.
Many adolescents are exposed to tobacco smoke, from either active smoking (CS) or secondhand smoke (SHS) exposure. Tobacco-specific biomarkers of exposure include cotinine (detects use in past 2-4 days) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL; detects use for a month or longer). NNAL is expected to detect more intermittent tobacco exposure. We compared NNAL and cotinine as biomarkers of exposure to tobacco in urban adolescents and determined the optimal NNAL cutoff point to distinguish CS from SHS exposure. Surplus urine samples, collected from 466 adolescents attending pediatric well or urgent care visits at Zuckerberg San Francisco General Hospital in 2013 to 2014, were assayed for cotinine and NNAL. Ninety-four percent of adolescents had measurable levels of NNAL compared with 87% for cotinine. The optimal NNAL cutoff point to distinguish CS from SHS was 9.6 pg/mL by latent class or 14.4 pg/mL by receiver-operating characteristic analysis. Cotinine and NNAL were strongly correlated, but the correlation slopes differed for active versus SHS-exposed adolescents. Among nonsmokers, NNAL levels were significantly higher in African American (median, 3.3 pg/mL) compared with other groups (0.9-1.9 pg/mL), suggesting greater exposure to SHS. Urine NNAL screening finds a large majority (94%) of urban adolescents are exposed to tobacco. African Americans are exposed to higher levels of SHS than other ethnic/racial groups. SHS is associated with significant medical morbidity in adolescents. Routine biochemical screening with NNAL or cotinine detects high prevalence of SHS exposure and should be considered as a tool to reduce SHS exposure in high-risk populations. .
许多青少年会接触到烟草烟雾,无论是主动吸烟(CS)还是二手烟(SHS)暴露。烟草特异性暴露生物标志物包括可替宁(检测过去 2-4 天的使用情况)和 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁醇(NNAL;检测一个月或更长时间的使用情况)。NNAL 预计能更准确地检测到间歇性的烟草暴露。我们比较了 NNAL 和可替宁作为城市青少年接触烟草的生物标志物,并确定了区分 CS 和 SHS 暴露的最佳 NNAL 截断点。2013 年至 2014 年,我们对在 Zuckerberg 旧金山总医院接受儿科常规或紧急护理就诊的 466 名青少年的尿液样本进行了可替宁和 NNAL 的检测。94%的青少年尿液中可检测到 NNAL,而可替宁的检出率为 87%。通过潜在类别分析,区分 CS 和 SHS 的最佳 NNAL 截断点为 9.6pg/ml,通过接收者操作特征分析为 14.4pg/ml。可替宁和 NNAL 呈强相关,但在 CS 和 SHS 暴露的青少年中,相关斜率不同。在不吸烟者中,非裔美国人(中位数为 3.3pg/ml)的 NNAL 水平明显高于其他群体(0.9-1.9pg/ml),这表明他们接触 SHS 的程度更高。尿 NNAL 筛查发现,绝大多数(94%)城市青少年接触过烟草。非裔美国人接触 SHS 的水平高于其他族裔/种族群体。SHS 与青少年的重大医疗发病有关。NNAL 或可替宁的常规生化筛查发现 SHS 暴露的高患病率,应将其视为减少高危人群 SHS 暴露的一种工具。