Genetic Epidemiology Group, International Agency for Research on Cancer, Lyon, France.
K.G. Jebsen Center for Genetic Epidemiology, Norwegian University of Science and Technology, Trondheim, Norway.
Int J Epidemiol. 2018 Dec 1;47(6):1760-1771. doi: 10.1093/ije/dyy100.
Self-reported smoking is the principal measure used to assess lung cancer risk in epidemiological studies. We evaluated if circulating cotinine-a nicotine metabolite and biomarker of recent tobacco exposure-provides additional information on lung cancer risk.
The study was conducted in the Lung Cancer Cohort Consortium (LC3) involving 20 prospective cohort studies. Pre-diagnostic serum cotinine concentrations were measured in one laboratory on 5364 lung cancer cases and 5364 individually matched controls. We used conditional logistic regression to evaluate the association between circulating cotinine and lung cancer, and assessed if cotinine provided additional risk-discriminative information compared with self-reported smoking (smoking status, smoking intensity, smoking duration), using receiver-operating characteristic (ROC) curve analysis.
We observed a strong positive association between cotinine and lung cancer risk for current smokers [odds ratio (OR ) per 500 nmol/L increase in cotinine (OR500): 1.39, 95% confidence interval (CI): 1.32-1.47]. Cotinine concentrations consistent with active smoking (≥115 nmol/L) were common in former smokers (cases: 14.6%; controls: 9.2%) and rare in never smokers (cases: 2.7%; controls: 0.8%). Former and never smokers with cotinine concentrations indicative of active smoking (≥115 nmol/L) also showed increased lung cancer risk. For current smokers, the risk-discriminative performance of cotinine combined with self-reported smoking (AUCintegrated: 0.69, 95% CI: 0.68-0.71) yielded a small improvement over self-reported smoking alone (AUCsmoke: 0.66, 95% CI: 0.64-0.68) (P = 1.5x10-9).
Circulating cotinine concentrations are consistently associated with lung cancer risk for current smokers and provide additional risk-discriminative information compared with self-report smoking alone.
自我报告的吸烟情况是评估流行病学研究中肺癌风险的主要指标。我们评估了循环中的可替宁(一种尼古丁代谢物和近期烟草暴露的生物标志物)是否提供了有关肺癌风险的额外信息。
该研究在肺癌队列联盟(LC3)中进行,涉及 20 项前瞻性队列研究。在一个实验室中对 5364 例肺癌病例和 5364 例个体匹配对照进行了预诊断前血清可替宁浓度的测量。我们使用条件逻辑回归评估了循环可替宁与肺癌之间的关联,并使用接受者操作特征(ROC)曲线分析评估了与自我报告的吸烟(吸烟状况、吸烟强度、吸烟持续时间)相比,可替宁是否提供了额外的风险判别信息。
我们观察到,当前吸烟者的可替宁与肺癌风险之间存在很强的正相关关系[每增加 500nmol/L 可替宁(OR500)的比值比(OR):1.39,95%置信区间(CI):1.32-1.47]。以前吸烟者(病例:14.6%;对照:9.2%)中常见可替宁浓度与主动吸烟一致(≥115nmol/L),而从不吸烟者(病例:2.7%;对照:0.8%)中则很少见。可替宁浓度表明有过主动吸烟(≥115nmol/L)的前吸烟者和从不吸烟者也表现出增加的肺癌风险。对于当前吸烟者,可替宁与自我报告的吸烟相结合(综合 AUC:0.69,95%CI:0.68-0.71)的风险判别性能优于单独使用自我报告的吸烟(AUCsmoke:0.66,95%CI:0.64-0.68)(P=1.5x10-9)。
循环可替宁浓度与当前吸烟者的肺癌风险始终相关,并与单独使用自我报告的吸烟相比提供了额外的风险判别信息。