Department of Chemistry, Faculty of Science, University of Malta, Msida MSD, 2080, Malta; Division of Cardiology, Clinical Pharmacology Program, Department of Medicine, University of California, San Francisco, CA, 94143, USA.
Division of Cardiology, Clinical Pharmacology Program, Department of Medicine, University of California, San Francisco, CA, 94143, USA.
Environ Res. 2022 Mar;204(Pt D):112405. doi: 10.1016/j.envres.2021.112405. Epub 2021 Nov 22.
School children may be exposed to secondhand smoke (SHS) either at home, in transit or in social gatherings permitting smoking in their presence. Questionnaires about SHS often underestimate prevalence and extent of exposure. A more accurate tool is the use of biomarkers such as cotinine (COT) and trans-3'-hydrocycotinine (3HC) as biomarkers of SHS exposure, alongside 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), a reduction product in the body of the tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), both potent carcinogens. We measured urinary COT, 3HC and total NNAL using sensitive and specific high-performance LC-MS/MS methods. The limit of quantification (LOQ) for each assay were 0.05 ng/mL, 0.1 ng/mL and 0.25 pg/mL respectively. The aim of this study was to evaluate the exposure to SHS of school children (9-11 years), from five public schools in the island of Malta, from questionnaire information about smoking at home and verify it by urinary biomarker data of COT, 3HC and NNAL. These biomarkers were measurable in 99.4%, 95.4% and 98.3% of the participating children respectively. From the children reporting smoking at home, 11% had a history of asthma and had COT, 3HC and NNAL geometric mean concentrations double compared to the non-asthmatic group. In has been confirmed that non-smokers exposed to SHS and THS have a higher NNAL/COT ratio than the group identified as smokers according to specific and defined COT threshold levels (despite the fact that a priori, the entire study group was composed of non-smokers). The implication of high measured levels of urinary NNAL in children should be of concern given its potency. A main effects multifactor ANOVA model was developed and the children's house and school locations and the smoking frequency were statistically significant to predict the levels of the three metabolites. For 3HC only, the status of the employment of the mother was also an important predictor.
儿童可能在家中、在上学途中或在允许吸烟的社交聚会上接触到二手烟(SHS)。有关 SHS 的调查问卷往往会低估流行率和接触程度。一种更准确的工具是使用生物标志物,如可替宁(COT)和反-3'-羟基可替宁(3HC)作为 SHS 暴露的生物标志物,以及 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁醇(NNAL),一种烟草特异性亚硝胺的体内还原产物,4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮(NNK),都是强致癌物质。我们使用灵敏和特异的高效液相色谱-串联质谱法(LC-MS/MS)测量尿液中的 COT、3HC 和总 NNAL。每个测定的定量下限(LOQ)分别为 0.05 ng/mL、0.1 ng/mL 和 0.25 pg/mL。本研究的目的是评估马耳他岛五所公立学校 9-11 岁儿童的 SHS 暴露情况,根据家庭吸烟情况的调查问卷信息进行验证,并通过尿液生物标志物 COT、3HC 和 NNAL 的数据进行验证。这些生物标志物在 99.4%、95.4%和 98.3%的参与儿童中均可测量。从报告在家中吸烟的儿童中,有 11%的儿童有哮喘病史,其 COT、3HC 和 NNAL 几何均数浓度是无哮喘组的两倍。已经证实,与根据特定和定义的 COT 阈值水平确定的吸烟者相比,接触 SHS 和 THS 的非吸烟者的 NNAL/COT 比值更高(尽管事实上,先验地,整个研究组都是由非吸烟者组成的)。考虑到 NNAL 的效力,儿童尿液中高浓度的 NNAL 应该引起关注。建立了一个主效应多因素方差分析模型,儿童的家庭和学校位置以及吸烟频率在统计学上对预测三种代谢物的水平具有显著意义。对于 3HC 而言,母亲的就业状况也是一个重要的预测因素。