Buchwald Jadwiga, Lehtimäki Terho, Raitakari Olli, Salomaa Veikko, Kaprio Jaakko, Pirinen Matti
Institute for Molecular Medicine Finland (FIMM), Helsinki Institute of Life Science (HiLIFE), University of Helsinki, Helsinki, Finland.
Department of Clinical Chemistry, Fimlab Laboratories, and Finnish Cardiovascular Research Center, Tampere, Finland.
Eur J Epidemiol. 2025 Jul 12. doi: 10.1007/s10654-025-01270-5.
Faster nicotine metabolism, defined as the nicotine metabolite ratio (NMR), is known to associate with heavier smoking and challenges in smoking cessation. However, the broader health implications of genetically determined nicotine metabolism are not well characterized. We performed a hypothesis-free phenome-wide association study (PheWAS) of over 21,000 outcome variables from UK Biobank (UKB) to explore how the NMR (measured as the 3-hydroxycotinine-to-cotinine ratio) associates with the phenome. As the exposure variable, we used a genetic score for faster nicotine metabolism based on 10 putative causal genetic variants, explaining 33.8 % of the variance in the NMR. We analysed ever and never smokers separately to assess whether a causal pathway through nicotine metabolism is plausible. A total of 57 outcome variables reached phenome-wide significance at a false discovery rate of 5 %. We observed expected associations with several phenotypes related to smoking and nicotine, but could not replicate prior findings on cessation. Importantly, we found novel associations between genetically determined faster nicotine metabolism and adverse health outcomes, including unfavourable liver enzyme and lipid values, as well as increased caffeine consumption. These associations did not appear to differ between ever and never smokers, suggesting the corresponding pathways may not involve nicotine metabolism. No favourable health outcomes were linked to genetically determined faster nicotine metabolism. Our findings support a possibility that a future smoking cessation therapy converting fast metabolizers of nicotine to slower ones could work without adverse side effects and potentially even provide other health-related benefits.
更快的尼古丁代谢,定义为尼古丁代谢物比率(NMR),已知与更大量吸烟及戒烟挑战相关。然而,基因决定的尼古丁代谢对更广泛健康的影响尚未得到充分描述。我们对英国生物银行(UKB)的21000多个结果变量进行了一项无假设的全表型关联研究(PheWAS),以探索NMR(以3-羟基可替宁与可替宁的比率衡量)与表型之间的关联。作为暴露变量,我们使用了基于10个假定因果基因变异的更快尼古丁代谢基因评分,该评分解释了NMR中33.8%的变异。我们分别分析了曾经吸烟者和从不吸烟者,以评估通过尼古丁代谢的因果途径是否合理。共有57个结果变量在5%的假发现率下达到全表型显著水平。我们观察到与一些与吸烟和尼古丁相关的表型有预期关联,但无法重复先前关于戒烟的研究结果。重要的是,我们发现基因决定的更快尼古丁代谢与不良健康结果之间存在新的关联,包括不利的肝酶和血脂值,以及咖啡因摄入量增加。这些关联在曾经吸烟者和从不吸烟者之间似乎没有差异,表明相应途径可能不涉及尼古丁代谢。没有有利的健康结果与基因决定的更快尼古丁代谢相关。我们的研究结果支持这样一种可能性,即未来将尼古丁快速代谢者转变为慢速代谢者的戒烟疗法可能有效且无不良副作用,甚至可能带来其他与健康相关的益处。