Endocrinology, Diabetology and Metabolism, Department of Internal Medicine, University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland.
Medical Outpatient Department, University Hospital Basel, Petersgraben 4, Basel, 4031, Switzerland.
Trials. 2023 Apr 20;24(1):284. doi: 10.1186/s13063-023-07164-9.
Cigarette smoking is the leading preventable cause of premature death. Despite dedicated programmes, quit rates remain low due to barriers such as nicotine withdrawal syndrome or post-cessation weight gain. Glucagon-like peptide-1 (GLP-1) analogues reduce energy intake and body weight and seem to modulate addictive behaviour. These GLP-1 properties are of major interest in the context of smoking cessation. The aim of this study is to evaluate the GLP-1 analogue dulaglutide as a new therapy for smoking cessation.
This is a placebo-controlled, double-blind, parallel group, superiority, single-centre randomized study including 255 patients. The intervention consists of a 12-week dulaglutide treatment phase with 1.5 mg once weekly or placebo subcutaneously, in addition to standard of care (behavioural counselling and pharmacotherapy with varenicline). A 40-week non-treatment phase follows. The primary outcome is the point prevalence abstinence rate at week 12. Smoking status is self-reported and biochemically confirmed by end-expiratory exhaled carbon monoxide measurement. Further endpoints include post-cessational weight gain, nicotine craving analysis, glucose homeostasis and long-term nicotine abstinence. Two separate substudies assess behavioural, functional and structural changes by functional magnetic resonance imaging and measures of energy metabolism (i.e. resting energy expenditure, body composition).
Combining behavioural counselling and medical therapy, e.g. with varenicline, improves abstinence rates and is considered the standard of care. We expect a further increase in quit rates by adding a second component of medical therapy and assume a dual effect of dulaglutide treatment (blunting nicotine withdrawal symptoms and reducing post-cessational weight gain). This project is of high relevance as it explores novel treatment options aimed at preventing the disastrous consequences of nicotine consumption and obesity.
ClinicalTrials.gov NCT03204396 . Registered on June 26, 2017.
吸烟是导致过早死亡的主要可预防原因。尽管有专门的项目,但由于尼古丁戒断综合征或戒烟后体重增加等障碍,戒烟率仍然很低。胰高血糖素样肽-1(GLP-1)类似物可减少能量摄入和体重,并似乎调节成瘾行为。这些 GLP-1 特性在戒烟方面具有重要意义。本研究旨在评估 GLP-1 类似物度拉糖肽作为一种新的戒烟治疗方法。
这是一项安慰剂对照、双盲、平行组、优效性、单中心随机研究,纳入了 255 名患者。干预措施包括为期 12 周的度拉糖肽治疗期,每周皮下注射 1.5mg,或安慰剂,此外还有标准护理(行为咨询和用伐尼克兰进行药物治疗)。随后是为期 40 周的非治疗期。主要结局是第 12 周的点患病率戒烟率。吸烟状况通过自我报告和呼出的终末呼气一氧化碳测量进行生物化学确认。其他终点包括戒烟后体重增加、尼古丁渴求分析、葡萄糖稳态和长期尼古丁戒断。两个单独的子研究通过功能磁共振成像和能量代谢测量(即静息能量消耗、身体成分)评估行为、功能和结构变化。
结合行为咨询和医疗治疗,例如使用伐尼克兰,可提高戒烟率,被认为是标准护理。我们预计通过添加第二种医疗治疗成分,戒烟率会进一步提高,并假设度拉糖肽治疗的双重作用(减轻尼古丁戒断症状和减少戒烟后体重增加)。该项目具有重要意义,因为它探索了旨在预防尼古丁消耗和肥胖灾难性后果的新治疗选择。
ClinicalTrials.gov NCT03204396。于 2017 年 6 月 26 日注册。