Motschman Courtney A, Gass Julie C, Wray Jennifer M, Germeroth Lisa J, Schlienz Nicolas J, Munoz Diana A, Moore Faith E, Rhodes Jessica D, Hawk Larry W, Tiffany Stephen T
Department of Psychology, University at Buffalo, The State University of New York, Park Hall, Buffalo, NY, 14260, USA.
Department of Psychology, University at Buffalo, The State University of New York, Park Hall, Buffalo, NY, 14260, USA; VA Center for Integrated Healthcare, VA Western NY Medical Center, Buffalo, NY, 14215, USA.
Drug Alcohol Depend. 2016 Dec 1;169:180-189. doi: 10.1016/j.drugalcdep.2016.10.018. Epub 2016 Oct 22.
The selection criteria used in clinical trials for smoking cessation and in laboratory studies that seek to understand mechanisms responsible for treatment outcomes may limit their generalizability to one another and to the general population.
We reviewed studies on varenicline versus placebo and compared eligibility criteria and participant characteristics of clinical trials (N=23) and laboratory studies (N=22) across study type and to nationally representative survey data on adult, daily USA smokers (2014 National Health Interview Survey; 2014 National Survey on Drug Use and Health).
Relative to laboratory studies, clinical trials more commonly reported excluding smokers who were unmotivated to quit and for specific medical conditions (e.g., cardiovascular disease, COPD), although both study types frequently reported excluding for general medical or psychiatric reasons. Laboratory versus clinical samples smoked less, had lower nicotine dependence, were younger, and more homogeneous with respect to smoking level and nicotine dependence. Application of common eligibility criteria to national survey data resulted in considerable elimination of the daily-smoking population for both clinical trials (≥47%) and laboratory studies (≥39%). Relative to the target population, studies in this review recruited participants who smoked considerably more and had a later smoking onset age, and were under-representative of Caucasians.
Results suggest that selection criteria of varenicline studies limit generalizability in meaningful ways, and differences in criteria across study type may undermine efforts at translational research. Recommendations for improvements in participant selection and reporting standards are discussed.
戒烟临床试验以及旨在了解治疗结果相关机制的实验室研究中所使用的选择标准,可能会限制它们彼此之间以及对一般人群的可推广性。
我们回顾了关于伐尼克兰对比安慰剂的研究,并比较了临床试验(N = 23)和实验室研究(N = 22)在研究类型方面的入选标准和参与者特征,并与美国成年每日吸烟者具有全国代表性的调查数据(2014年国家健康访谈调查;2014年国家药物使用和健康调查)进行了比较。
相对于实验室研究,临床试验更常报告排除没有戒烟意愿的吸烟者以及患有特定疾病(如心血管疾病、慢性阻塞性肺疾病)的吸烟者,尽管两种研究类型都经常报告因一般医疗或精神原因而排除某些参与者。实验室样本与临床样本相比,吸烟量更少,尼古丁依赖性更低,年龄更小,在吸烟水平和尼古丁依赖性方面更具同质性。将常见的入选标准应用于全国调查数据,导致临床试验(≥47%)和实验室研究(≥39%)的每日吸烟人群大量减少。相对于目标人群,本综述中的研究招募的参与者吸烟量明显更多且吸烟起始年龄更晚,并且白种人代表性不足。
结果表明,伐尼克兰研究的选择标准在很大程度上限制了可推广性,并且不同研究类型的标准差异可能会破坏转化研究的努力。文中讨论了改进参与者选择和报告标准的建议。