Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH) and Departments of Psychiatry, Pharmacology and Toxicology, University of Toronto, Toronto, M5S 1A8, Ontario, Canada.
Trends Mol Med. 2018 Feb;24(2):187-196. doi: 10.1016/j.molmed.2017.12.001. Epub 2018 Jan 4.
Clinical medicine of the future is poised to use an individual's genomic data to predict disease risk and guide clinical care. The treatment of cigarette smoking and tobacco use disorder represents a prime area for genomics implementation. The genes CHRNA5 and CYP2A6 are strong genomic contributors that alter the risk of heaviness of smoking, tobacco use disorder, and smoking-related diseases in humans. These biomarkers have proven analytical and clinical validity, and evidence for their clinical utility continues to grow. We propose that these biomarkers harbor the potential of enabling the identification of elevated disease risk in smokers, personalizing smoking cessation treatments, and motivating behavioral changes. We must prepare for the integration of genomic applications into clinical care of patients who smoke.
未来的临床医学将利用个体的基因组数据来预测疾病风险并指导临床护理。治疗吸烟和烟草使用障碍是基因组学实施的主要领域。CHRNA5 和 CYP2A6 基因是改变吸烟严重程度、烟草使用障碍和与吸烟相关疾病风险的重要基因组贡献者。这些生物标志物具有经过验证的分析和临床有效性,并且其临床实用性的证据不断增加。我们提出这些生物标志物有可能使我们能够识别出吸烟者的疾病风险增加,使戒烟治疗更加个性化,并促进行为改变。我们必须为将基因组应用整合到吸烟患者的临床护理中做好准备。