Ashare Rebecca L, Lerman Caryn, Tyndale Rachel F, Hawk Larry W, George Tony P, Cinciripini Paul, Schnoll Robert A
Department of Psychiatry, University of Pennsylvania, 3535 Market Street, Suite 4100, Philadelphia, PA, 19104.
Department of Psychiatry and Abramson Cancer Center, University of Pennsylvania, 3535 Market Street, Suite 4100, Philadelphia, PA, 19104.
J Smok Cessat. 2017 Jun;12(2):63-70. doi: 10.1017/jsc.2016.11. Epub 2016 Apr 12.
The nicotine-metabolite ratio (NMR) predicts treatment response and is related to treatment side effect severity. Sleep disturbance may be one important side effect, but understanding sleep disturbance effects on smoking cessation is complicated by the fact that nicotine withdrawal also produces sleep disturbance.
To evaluate the effects of withdrawal and treatment side effects on sleep disturbance.
This is a secondary analysis of data from a clinical trial (Lerman et al., 2015) of 1,136 smokers randomised to placebo ( = 363), transdermal nicotine (TN; = 381), or varenicline ( = 392) and stratified based on NMR (559 slow metabolisers; 577 normal metabolisers). Sleep disturbance was assessed at baseline and at 1-week following the target quit date (TQD). We also examined whether sleep disturbance predicted 7-day point-prevalence abstinence at end-of-treatment (EOT).
The varenicline and TN groups exhibited greater increases in sleep disturbance (vs. placebo; treatment × time interaction; = 0.005), particularly among those who quit smoking at 1-week post-TQD. There was a main effect of NMR ( = 0.04), but no interactions with treatment. TN and varenicline attenuated withdrawal symptoms unrelated to sleep (vs. placebo). Greater baseline sleep disturbance predicted relapse at EOT ( = 0.004).
Existing treatments may not mitigate withdrawal-related sleep disturbance and adjunctive treatments that target sleep disturbance may improve abstinence rates.
尼古丁代谢物比率(NMR)可预测治疗反应,并与治疗副作用的严重程度相关。睡眠障碍可能是一种重要的副作用,但由于尼古丁戒断也会导致睡眠障碍,因此了解睡眠障碍对戒烟的影响变得复杂。
评估戒断和治疗副作用对睡眠障碍的影响。
这是一项对来自一项临床试验(Lerman等人,2015年)数据的二次分析,该试验将1136名吸烟者随机分为安慰剂组(n = 363)、经皮尼古丁组(TN;n = 381)或伐尼克兰组(n = 392),并根据NMR进行分层(559名慢代谢者;577名正常代谢者)。在基线和目标戒烟日期(TQD)后1周评估睡眠障碍情况。我们还检查了睡眠障碍是否能预测治疗结束时(EOT)的7天点患病率戒烟情况。
伐尼克兰组和TN组的睡眠障碍增加幅度更大(与安慰剂相比;治疗×时间交互作用;P = 0.005),尤其是在TQD后1周戒烟的人群中。NMR有主效应(P = 0.04),但与治疗无交互作用。TN和伐尼克兰减轻了与睡眠无关的戒断症状(与安慰剂相比)。基线睡眠障碍程度越高,预测EOT时复发的可能性越大(P = 0.004)。
现有治疗方法可能无法减轻与戒断相关的睡眠障碍,针对睡眠障碍的辅助治疗可能会提高戒烟率。