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纳曲酮对尼古丁依赖的男性和女性戒烟效果及体重增加的影响。

Effects of naltrexone on smoking cessation outcomes and weight gain in nicotine-dependent men and women.

机构信息

Department of Psychiatry & Behavioral Neuroscience, University of Chicago, Chicago, IL 60637, USA.

出版信息

J Clin Psychopharmacol. 2012 Oct;32(5):630-6. doi: 10.1097/JCP.0b013e3182676956.

Abstract

This study examined whether the opioid receptor antagonist naltrexone is efficacious in smoking cessation and whether sex moderates the response. We assessed smoking quit rates and weight gain in a double-blind randomized trial comparing oral naltrexone (n = 162) with placebo (n = 154) in nicotine-dependent participants who wanted to quit smoking. The medication was gradually titrated up to 50 mg during the week before the quit date and then maintained at this dose for 12 weeks. For the first 4 weeks after the quit date, all participants received a nicotine patch to mitigate tobacco withdrawal and attended weekly individual cognitive-behavioral smoking cessation counseling sessions. After this time, participants continued with naltrexone or placebo through 12 weeks. Follow-up assessments were conducted at 26 and 52 weeks. During treatment, naltrexone (vs placebo) increased quit rates, attenuated smoking urge, and reduced weight gain. At follow-up, after medication discontinuation, the effect of naltrexone on improving quit rates was no longer evident. Men and women experienced different benefits from naltrexone; men showed greater reductions in smoking, whereas women showed greater reductions in weight gain. In sum, naltrexone showed acute efficacy in treating nicotine dependence, but after the medication was discontinued, the effect on quit rate was not maintained. Further study of naltrexone in smoking cessation treatment and reduction of cessation-related weight gain, as well as preclinical investigation of mechanisms underlying sex differences, is warranted.

摘要

这项研究旨在探讨阿片受体拮抗剂纳曲酮在戒烟中的疗效,以及性别是否调节其反应。我们在一项双盲随机试验中评估了吸烟戒断率和体重增加情况,该试验比较了口服纳曲酮(n = 162)与安慰剂(n = 154)在想要戒烟的尼古丁依赖参与者中的效果。在戒烟日期前的一周内,逐渐将药物滴定至 50mg,然后维持此剂量 12 周。在戒烟日期后的前 4 周,所有参与者都接受尼古丁贴片以减轻烟草戒断症状,并参加每周一次的个体认知行为戒烟咨询。此后,参与者继续服用纳曲酮或安慰剂 12 周。随访评估在 26 周和 52 周进行。在治疗期间,纳曲酮(与安慰剂相比)提高了戒烟率,减轻了吸烟冲动,并减少了体重增加。在随访时,停药后,纳曲酮对提高戒烟率的效果不再明显。男性和女性从纳曲酮中获得的益处不同;男性的吸烟量减少幅度更大,而女性的体重增加幅度减少幅度更大。总之,纳曲酮在治疗尼古丁依赖方面具有急性疗效,但停药后,对戒烟率的影响无法维持。需要进一步研究纳曲酮在戒烟治疗和减少与戒烟相关的体重增加方面的作用,以及对性别差异背后机制的临床前研究。

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