Exploring Predictors of Treatment Response to GLP-1 Receptor Agonists for Smoking Cessation.

IF 3 2区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Luba Yammine, Constanza de Dios, Robert Suchting, Charles E Green, David A Nielsen, Consuelo Walss-Bass, Joy M Schmitz
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引用次数: 0

Abstract

Introduction: Understanding predictors of smoking cessation medication efficacy facilitates the ability to enhance treatment effectiveness. In our pilot trial, exenatide, a glucagon-like peptide-1 receptor agonist, adjunct to nicotine patch improved smoking abstinence compared to nicotine patch alone. This secondary analysis explores potential baseline characteristics associated with differential treatment response to exenatide.

Methods: The parent trial randomized (1:1) 84 smokers with prediabetes and/or overweight to once-weekly placebo or exenatide, 2 mg, subcutaneously. All participants received nicotine patch (21 mg) and brief smoking cessation counseling, with biologically confirmed 7-day point prevalence abstinence at week 6 (end-of-treatment) deemed the primary outcome. Bayesian generalized linear modeling explored differential response to treatment as a function of baseline patient characteristics, including demographic, psychosocial, clinical, smoking related, and genetic factors. Posterior probability (PP)≥75% that an effect exists was taken as a minimum threshold of evidence in favor of model effects.

Results: Exenatide showed stronger benefit versus placebo in participants that smoked >20 cigarettes per day (PP=81.7%) and in those without prediabetes (PP=76.0%) or obesity (PP=94.4%). Exenatide's efficacy was observed only in individuals with no/minimal depression symptoms but not in those with symptoms (PP=91.2%). Finally, exenatide was more efficacious than placebo only in those with the CHRNA rs16969968 GG genotype (PP=88.6%).

Conclusions: The effect of exenatide on abstinence may be moderated by the number of cigarettes smoked daily, metabolic, psychological, and genetic factors. Larger prospective investigations are needed to confirm and extend these findings.

Implications: Understanding predictors of smoking cessation medication efficacy enhances the ability to improve treatment effectiveness. In our pilot trial, extended-release exenatide, a GLP-1 receptor agonist, adjunct to nicotine patch, improved smoking abstinence in smokers with prediabetes and/or overweight. The current post-hoc analysis found that the effect of exenatide on smoking abstinence may be moderated by the number of cigarettes smoked daily, metabolic, psychological, and genetic factors. Larger investigations are needed to confirm and extend these findings.

探索GLP-1受体激动剂对戒烟治疗反应的预测因素。
前言:了解戒烟药物疗效的预测因素有助于提高治疗效果。在我们的试点试验中,艾塞那肽,一种胰高血糖素样肽-1受体激动剂,与尼古丁贴片相比,辅助尼古丁贴片改善了戒烟效果。这一次要分析探讨了与艾塞那肽不同治疗反应相关的潜在基线特征。方法:父母试验随机(1:1)84名糖尿病前期和/或超重的吸烟者,每周一次皮下注射安慰剂或艾塞那肽2毫克。所有参与者都接受了尼古丁贴片(21毫克)和简短的戒烟咨询,在第6周(治疗结束)生物学证实的7天点流行戒烟被视为主要结果。贝叶斯广义线性模型探讨了作为基线患者特征函数的治疗差异反应,包括人口统计学、社会心理、临床、吸烟相关和遗传因素。效应存在的后验概率(PP)≥75%作为支持模型效应的最小证据阈值。结果:艾塞那肽在每天吸烟20支(PP=81.7%)和没有糖尿病前期(PP=76.0%)或肥胖(PP=94.4%)的参与者中显示出比安慰剂更强的益处。艾塞那肽的疗效仅在没有或只有轻微抑郁症状的个体中观察到,而在有抑郁症状的个体中没有观察到(PP=91.2%)。最后,在CHRNA rs16969968 GG基因型患者中,艾塞那肽比安慰剂更有效(PP=88.6%)。结论:艾塞那肽对戒烟的影响可能受每日吸烟数量、代谢、心理和遗传因素的影响。需要更大规模的前瞻性调查来证实和扩展这些发现。意义:了解戒烟药物疗效的预测因素有助于提高治疗效果。在我们的试点试验中,缓释艾塞那肽,一种GLP-1受体激动剂,辅助尼古丁贴片,改善了糖尿病前期和/或超重吸烟者的戒烟效果。目前的事后分析发现,艾塞那肽对戒烟的影响可能受到每日吸烟数量、代谢、心理和遗传因素的影响。需要更大规模的调查来证实和扩展这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nicotine & Tobacco Research
Nicotine & Tobacco Research 医学-公共卫生、环境卫生与职业卫生
CiteScore
8.10
自引率
10.60%
发文量
268
审稿时长
3-8 weeks
期刊介绍: Nicotine & Tobacco Research is one of the world''s few peer-reviewed journals devoted exclusively to the study of nicotine and tobacco. It aims to provide a forum for empirical findings, critical reviews, and conceptual papers on the many aspects of nicotine and tobacco, including research from the biobehavioral, neurobiological, molecular biologic, epidemiological, prevention, and treatment arenas. Along with manuscripts from each of the areas mentioned above, the editors encourage submissions that are integrative in nature and that cross traditional disciplinary boundaries. The journal is sponsored by the Society for Research on Nicotine and Tobacco (SRNT). It publishes twelve times a year.
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