Duc Huy Le, Hui Cai, Danxia Yu, Sang Minh Nguyen, Wei Zheng, Qiuyin Cai, Xiao-Ou Shu
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引用次数: 0
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.