Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
Hurvitz Brain Sciences Program, Sunnybrook Research Institute, Toronto, ON, Canada.
Addiction. 2020 Jan;115(1):134-144. doi: 10.1111/add.14810. Epub 2019 Nov 5.
Varenicline effectiveness may be related to the level of adherence, which might be reduced by adverse effects such as nausea. The aim of the study was to test a possible effect of nausea on smoking cessation outcomes mediated by adherence.
Mediation path analysis.
Multiple sites within Canada and the United States.
Treatment-seeking smokers receiving varenicline from two smoking cessation clinical trials: Quit2Live (NCT01836276; n = 449) and Pharmacogenetics of Nicotine Addiction Treatment (PNAT) (NCT01314001; n = 421).
Nausea severity was collected through self-report and adherence was biologically assessed using varenicline concentrations (Quit2Live, plasma sample at week 4; PNAT, saliva sample at week 2). In Quit2Live, the end-points were cotinine-verified abstinence at weeks 4, 12 and 26. In PNAT, the end-points were carbon monoxide-verified abstinence at weeks 2, 12 and 26.
Early nausea was not directly associated with abstinence [odds ratio (OR) ranging from 0.73-1.28; P ≥ 0.26]. However early nausea was indirectly associated with lower cessation rates at multiple timepoints (ORs ranging from 0.92-0.94; 95% CI between 0.83-0.99) in a relationship mediated by reduced varenicline adherence (assessed by plasma varenicline concentrations) in the primary trial (Quit2Live). This relationship between nausea, adherence and cessation was similar in direction but weaker in effect size (ORs ranging from 0.98-0.99; 95% CI between 0.90-1.03) in a secondary trial (PNAT), where adherence was assessed using salivary varenicline concentrations.
These data suggest that early nausea during varenicline treatment may be indirectly associated with lower likelihood of smoking cessation through reducing varenicline adherence. Differences in robustness between the trials may be due to the different biological matrices (plasma vs. saliva) and/or timing used to assess varenicline adherence. The results of the first study suggest that improved management of early nausea during varenicline treatment may positively impact smoking cessation success through increasing varenicline adherence.
伐伦克林的有效性可能与依从性有关,而依从性可能会因恶心等不良反应而降低。本研究旨在测试恶心对戒烟结果的可能影响,以及这种影响是否通过依从性来介导。
中介路径分析。
加拿大和美国的多个地点。
来自两项戒烟临床试验的接受伐伦克林治疗的吸烟参与者:Quit2Live(NCT01836276;n=449)和尼古丁成瘾治疗的药物遗传学(PNAT)(NCT01314001;n=421)。
恶心严重程度通过自我报告收集,通过伐伦克林浓度(Quit2Live,第 4 周的血浆样本;PNAT,第 2 周的唾液样本)来评估依从性。在 Quit2Live 中,终点是在第 4、12 和 26 周时通过可替宁验证的戒烟。在 PNAT 中,终点是在第 2、12 和 26 周时通过一氧化碳验证的戒烟。
早期恶心与戒烟率无直接关联[比值比(OR)范围为 0.73-1.28;P≥0.26]。然而,在主要试验(Quit2Live)中,早期恶心与多次戒烟率降低呈间接相关(OR 范围为 0.92-0.94;95%CI 为 0.83-0.99),这种关系是通过降低伐伦克林的依从性(通过评估血浆中的伐伦克林浓度)介导的。在次要试验(PNAT)中,这种恶心、依从性和戒烟之间的关系在方向上相似,但在效果大小上较弱(OR 范围为 0.98-0.99;95%CI 为 0.90-1.03),在该试验中,通过唾液中的伐伦克林浓度来评估依从性。
这些数据表明,伐伦克林治疗期间的早期恶心可能通过降低伐伦克林的依从性,间接地与戒烟可能性降低相关。试验之间的稳健性差异可能是由于使用不同的生物基质(血浆与唾液)和/或时间来评估伐伦克林的依从性。第一项研究的结果表明,通过改善伐伦克林治疗期间的早期恶心管理,可能通过提高伐伦克林的依从性来积极影响戒烟的成功。