Ann Intern Med. 2013 Sep 17;159(6):390-400. doi: 10.7326/0003-4819-159-6-201309170-00005.
Chinese translation
Depression is overrepresented in smokers.
To evaluate smoking abstinence and changes in mood and anxiety levels in smokers with depression treated with varenicline versus placebo.
Phase 4, multicenter, parallel, 1:1 allocation, double-blind, randomization trial. Randomization, stratified by antidepressant use and depression score at baseline, was blocked in sizes of 4. (ClinicalTrials.gov: NCT01078298).
38 centers in 8 countries.
525 adult smokers with stably treated current or past major depression and no recent cardiovascular events.
Varenicline, 1 mg twice daily, or placebo for 12 weeks, with 40-week nontreatment follow-up.
Primary outcome was carbon monoxide-confirmed continuous abstinence rate (CAR) for weeks 9 to 12. Other outcomes included CARs assessed during nontreatment follow-up and ratings of mood, anxiety, and suicidal ideation or behavior.
68.4% versus 66.5% of the varenicline and placebo groups, respectively, completed the study. Varenicline-treated participants had higher CARs versus placebo at weeks 9 to 12 (35.9% vs. 15.6%; odds ratio [OR], 3.35 [95% CI, 2.16 to 5.21]; P < 0.001), 9 to 24 (25.0% vs. 12.3%; OR, 2.53 [CI, 1.56 to 4.10]; P < 0.001), and 9 to 52 (20.3% vs. 10.4%; OR, 2.36 [CI, 1.40 to 3.98]; P = 0.001). There were no clinically relevant differences between groups in suicidal ideation or behavior and no overall worsening of depression or anxiety in either group. The most frequent adverse event was nausea (varenicline, 27.0%; placebo, 10.4%). Two varenicline-group participants died during the nontreatment phase.
Some data were missing, and power to detect differences between groups was low in rare events. Smokers with untreated depression, with co-occurring psychiatric conditions, or receiving mood stabilizers and antipsychotics were not included.
Varenicline increased smoking cessation in smokers with stably treated current or past depression without exacerbating depression or anxiety.
Pfizer.
背景:抑郁症在吸烟者中较为常见。
目的:评估安非他酮与安慰剂治疗抑郁症吸烟者的戒烟率和情绪及焦虑水平变化。
设计:这是一项 4 期、多中心、平行、1:1 分配、双盲、随机临床试验。根据抗抑郁药的使用情况和基线时的抑郁评分,按 4 例进行分层随机化。(临床试验.gov:NCT01078298)。
地点:8 个国家的 38 个中心。
参与者:525 名患有稳定治疗的当前或过去重度抑郁症且近期无心血管事件的成年吸烟者。
干预措施:安非他酮,每日 2 次,每次 1 毫克,或安慰剂治疗 12 周,不治疗随访 40 周。
测量:主要结局为第 9 至 12 周时碳 monoxide-confirmed 连续戒烟率(CAR)。其他结局包括不治疗随访期间评估的 CAR 以及情绪、焦虑和自杀意念或行为的评分。
结果:分别有 68.4%和 66.5%的安非他酮和安慰剂组完成了研究。与安慰剂组相比,安非他酮组在第 9 至 12 周(35.9%对 15.6%;优势比[OR],3.35[95%置信区间,2.16 至 5.21];P<0.001)、第 9 至 24 周(25.0%对 12.3%;OR,2.53[置信区间,1.56 至 4.10];P<0.001)和第 9 至 52 周(20.3%对 10.4%;OR,2.36[置信区间,1.40 至 3.98];P=0.001)的 CAR 更高。两组在自杀意念或行为方面没有临床相关差异,两组的抑郁或焦虑均无总体恶化。最常见的不良事件是恶心(安非他酮,27.0%;安慰剂,10.4%)。两名安非他酮组参与者在不治疗期间死亡。
局限性:部分数据缺失,罕见事件组间差异的检测能力较低。未纳入未经治疗的抑郁症、同时存在精神疾病或正在接受情绪稳定剂和抗精神病药物治疗的吸烟者。
结论:安非他酮增加了稳定治疗当前或过去抑郁症吸烟者的戒烟率,且不会加重抑郁或焦虑。
主要资金来源:辉瑞公司。