Ross Kathryn C, Gubner Noah R, Tyndale Rachel F, Hawk Larry W, Lerman Caryn, George Tony P, Cinciripini Paul, Schnoll Robert A, Benowitz Neal L
Center for Tobacco Control Research and Education, University of California San Francisco, San Francisco, CA, USA.
Centre for Addiction and Mental Health and Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada; Department of Pharmacology & Toxicology, University of Toronto, Toronto, Ontario, Canada.
Pharmacol Biochem Behav. 2016 Sep;148:1-7. doi: 10.1016/j.pbb.2016.05.002. Epub 2016 May 11.
Rate of nicotine metabolism has been identified as an important factor influencing nicotine intake and can be estimated using the nicotine metabolite ratio (NMR), a validated biomarker of CYP2A6 enzyme activity. Individuals who metabolize nicotine faster (higher NMR) may alter their smoking behavior to titrate their nicotine intake in order to maintain similar levels of nicotine in the body compared to slower nicotine metabolizers. There are known racial differences in the rate of nicotine metabolism with African Americans on average having a slower rate of nicotine metabolism compared to Whites. The goal of this study was to determine if there are racial differences in the relationship between rate of nicotine metabolism and measures of nicotine intake assessed using multiple biomarkers of nicotine and tobacco smoke exposure. Using secondary analyses of the screening data collected in a recently completed clinical trial, treatment-seeking African American and White daily smokers (10 or more cigarettes per day) were grouped into NMR quartiles so that the races could be compared at the same NMR, even though the distribution of NMR within race differed. The results indicated that rate of nicotine metabolism was a more important factor influencing nicotine intake in White smokers. Specifically, Whites were more likely to titrate their nicotine intake based on the rate at which they metabolize nicotine. However, this relationship was not found in African Americans. Overall there was a greater step-down, linear type relationship between NMR groups and cotinine or cotinine/cigarette in African Americans, which is consistent with the idea that differences in blood cotinine levels between the African American NMR groups were primarily due to differences in CYP2A6 enzyme activity without titration of nicotine intake among faster nicotine metabolizers.
尼古丁代谢率已被确定为影响尼古丁摄入量的一个重要因素,并且可以使用尼古丁代谢物比率(NMR)来估计,NMR是一种经过验证的CYP2A6酶活性生物标志物。尼古丁代谢较快(NMR较高)的个体可能会改变他们的吸烟行为,以调节尼古丁摄入量,从而与尼古丁代谢较慢的个体相比,维持体内相似的尼古丁水平。已知尼古丁代谢率存在种族差异,与白人相比,非裔美国人的尼古丁代谢率平均较慢。本研究的目的是确定在使用尼古丁和烟草烟雾暴露的多种生物标志物评估的尼古丁代谢率与尼古丁摄入量测量值之间的关系中是否存在种族差异。通过对最近完成的一项临床试验中收集的筛查数据进行二次分析,寻求治疗的非裔美国和白人每日吸烟者(每天吸10支或更多香烟)被分为NMR四分位数组,以便即使种族内NMR分布不同,也能在相同的NMR水平上比较种族。结果表明,尼古丁代谢率是影响白人吸烟者尼古丁摄入量的更重要因素。具体而言,白人更有可能根据他们代谢尼古丁的速度来调节尼古丁摄入量。然而,在非裔美国人中未发现这种关系。总体而言,非裔美国人的NMR组与可替宁或可替宁/香烟之间存在更大的逐步下降的线性关系,这与以下观点一致,即非裔美国人NMR组之间血液可替宁水平的差异主要是由于CYP2A6酶活性的差异,而尼古丁代谢较快者中尼古丁摄入量没有调节。