Department of Experimental and Clinical Pharmacology, University of Rzeszów, Rzeszów, Poland.
Laboratory for Innovative Research in Pharmacology, University of Rzeszów, Rzeszów, Poland.
Addiction. 2019 Nov;114(11):1951-1969. doi: 10.1111/add.14721. Epub 2019 Jul 19.
To review cytisine's history of use, pre-clinical evidence, clinical pharmacokinetics, efficacy, adverse reactions (ARs) and safety for smoking cessation.
A synoptic review of the use of cytisine as a smoking cessation medication, mechanism of action, pharmacokinetics and safety. Relevant literature on data included in these sections were identified through a search of 11 databases with additional literature obtained from reports and monographs. Three databases (PubMed, EMBASE and www.elibrary.ru) were systematically searched for studies published from 2012 to August 2018 in any language to provide an updated meta-analysis of cytisine's efficacy and ARs for smoking cessation compared with placebo. We pooled the relative risks (RR) of abstinence in the efficacy analysis and RR of ARs, either reported by the authors or calculated from the reports.
Cytisine has been in use since 1964 and is currently marketed in 18 countries. Systemic bioavailability from oral ingestion is high and clearance is primarily renal, with minimal or no metabolism. Brain uptake in animal models is moderate. The plasma half-life averages 4.8 hours. Eight studies were included for meta-analysis of efficacy. With heterogeneous results, the overall RR versus placebo of successful continuous abstinence at the longest follow-up was 1.74 [95% confidence interval (CI) = 1.38-2.19]. Nausea, vomiting, dyspepsia, upper abdominal pain and dry mouth that were mild or moderate were the most common ARs, with RR versus placebo 1.10 (95% CI = 0.95-1.28). The cost of cytisine in eastern and central Europe is several-fold less than that of other smoking cessation medications.
Cytisine is a low-cost medication found to increase the likelihood of smoking cessation. The most frequently reported ARs of cytisine involve gastrointestinal symptoms that are mostly reported as either mild or moderate in severity.
综述烟碱类似物 cytisine 用于戒烟的历史、临床前证据、临床药代动力学、疗效、不良反应(ARs)和安全性。
对 cytisine 作为戒烟药物的使用、作用机制、药代动力学和安全性进行综合评价。通过 11 个数据库检索纳入章节相关文献,并从报告和专着中获取额外文献。在 2012 年至 2018 年 8 月期间,以任何语言在 3 个数据库(PubMed、EMBASE 和 www.elibrary.ru)中系统检索研究,以提供 cytisine 与安慰剂相比在戒烟方面的疗效和 ARs 的更新荟萃分析。我们对疗效分析中 abstinence 的相对风险(RR)和 ARs 的 RR 进行了汇总,RR 要么是作者报告的,要么是从报告中计算得出的。
cytisine 自 1964 年以来一直在使用,目前在 18 个国家销售。口服摄入后的全身生物利用度高,清除主要通过肾脏,代谢很少或没有。在动物模型中脑摄取量中等。血浆半衰期平均为 4.8 小时。有 8 项研究被纳入meta 分析以评估疗效。结果具有异质性,最长随访时与安慰剂相比成功持续戒烟的总体 RR 为 1.74[95%置信区间(CI)=1.38-2.19]。恶心、呕吐、消化不良、上腹痛和口干是最常见的 ARs,与安慰剂相比 RR 为 1.10(95%CI=0.95-1.28)。东欧和中欧 cytisine 的价格比其他戒烟药物低几倍。
cytisine 是一种低成本药物,可提高戒烟的可能性。cytisine 最常报告的 ARs 涉及胃肠道症状,这些症状大多报告为轻度或中度。