Covey L S, Glassman A H, Stetner F
New York State Psychiatric Institute, Department of Psychiatry, College of Physicians and Surgeons, Columbia University 10032, USA.
J Addict Dis. 1999;18(1):31-40. doi: 10.1300/J069v18n01_04.
This study examined the efficacy of naltrexone, a long-acting opiate antagonist, as a smoking cessation aid in a double-blind placebo-controlled randomized trial. It was hypothesized that naltrexone would result in higher quit rates at the end of treatment and six months later.
Subjects were 68 smokers aged 18 to 65 who smoked at least 20 cigarettes daily and wished to stop smoking. They took naltrexone or placebo daily for four weeks and were seen weekly for individual smoking cessation therapy.
A statistical trend towards a higher overall cessation rate (cotinine < 15 ng/mL) at end-of-treatment was observed among subjects treated with naltrexone than placebo (46.7% vs. 26.3%, respectively, odds ratio = 2.5, p < .10); however, this difference was attenuated at six months (27% vs. 15%, respectively, odds ratio = 1.9, p = ns). Stratified analysis indicated the usefulness of naltrexone primarily for female smokers and those with a history of major depression. These effects remained six months later.
These results provide, at best, mild promise for naltrexone as a smoking cessation drug and provide another instance of a differential response to nicotine dependence treatment according to gender and depression history.
本研究在一项双盲安慰剂对照随机试验中,检验了长效阿片类拮抗剂纳曲酮作为戒烟辅助药物的疗效。研究假设纳曲酮在治疗结束时及六个月后会带来更高的戒烟率。
研究对象为68名年龄在18至65岁之间、每天至少吸20支烟且希望戒烟的吸烟者。他们每天服用纳曲酮或安慰剂,持续四周,并每周接受一次个体戒烟治疗。
在治疗结束时,接受纳曲酮治疗的受试者的总体戒烟率(可替宁<15 ng/mL)相较于安慰剂组有统计学上的升高趋势(分别为46.7%和26.3%,优势比=2.5,p<.10);然而,这种差异在六个月时有所减弱(分别为27%和15%,优势比=1.9,p=无统计学意义)。分层分析表明,纳曲酮主要对女性吸烟者和有重度抑郁病史的吸烟者有效。这些效果在六个月后依然存在。
这些结果充其量为纳曲酮作为戒烟药物提供了微弱的前景,并提供了另一个根据性别和抑郁病史对尼古丁依赖治疗有不同反应的实例。