Associations between Metabolomic Signatures of Persistent Smoking Effects and Lung Cancer Risk among Former Smokers.

IF 3.4
Duc Huy Le, Hui Cai, Danxia Yu, Sang Minh Nguyen, Wei Zheng, Qiuyin Cai, Xiao-Ou Shu
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Abstract

Background: Smoking-related metabolic perturbations may persist long after smoking cessation. We aimed to develop a metabolomic signature for persistent smoking (MSPS) and prospectively assess its association with lung cancer risk among former smokers.

Methods: Global untargeted metabolomic data from 1,732 participants of the Shanghai Men's Health Study (SMHS) and Southern Community Cohort Study (SCCS) were used to construct MSPS. Linear regression and elastic net regression were applied to select persistent smoking-related metabolites and develop MSPS. We evaluated the association of MSPS with lung cancer via conditional logistic regression among 229 case-control pairs nested in former smokers of the SCCS and SMHS.

Results: We identified 130 metabolites significantly associated with current smoking status (PFDR < 0.05). After excluding tobacco-specific metabolites, we selected 16 metabolites associated with former smoking (6 lipids, 6 xenobiotics, 2 amino acids, and 2 carbohydrates) to derive the MSPS. The MSPS showed a significant association with increased lung cancer risk [odds ratio (OR); 95% confidence interval (CI), 1.44 (1.15-1.81) per standard deviation (SD)], independent of smoking pack-years and quitting duration. The association was consistently seen in Whites (OR = 1.91; 95% CI, 1.19-3.07 per SD), Blacks (OR = 1.66; 95% CI, 1.07-2.56 per SD), and Asians (OR = 1.15; 95% CI, 0.81-1.63 per SD).

Conclusions: We developed an MSPS that was robustly associated with lung cancer risk independent of smoking history for former smokers. If validated, the MSPS can be applied to identify former smokers at high risk of developing lung cancer.

Impact: The MSPS provides a novel tool to stratify lung cancer risk among former smokers, beyond current guidelines based on smoking history.

前吸烟者中持续吸烟影响的代谢组学特征与肺癌风险之间的关系。
背景:吸烟相关的代谢紊乱可能在戒烟后持续很长时间。我们旨在开发一种捕获持续吸烟效应(MSPS)的代谢物特征,并前瞻性地评估其与前吸烟者肺癌(LC)风险的关系。方法:利用上海男性健康研究(SMHS)和南方社区队列研究(SCCS)的1732名参与者的全球非靶向代谢组学数据构建MSPS。采用线性回归和弹性网回归筛选与持续吸烟相关的代谢物,形成MSPS。我们通过条件逻辑回归对229对嵌套在SCCS和SMHS前吸烟者中的病例对照进行了MSPS与LC的关联评估。结果:我们确定了130种与当前吸烟状态显著相关的代谢物(pfdr)。结论:我们开发了一种与前吸烟者的LC风险密切相关的MSPS,与吸烟史无关。如果得到验证,MSPS可用于识别有高风险发展为LC的前吸烟者。影响:MSPS提供了一种新的工具来对前吸烟者的LC风险进行分层,超越了目前基于吸烟史的指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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