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辛伐他汀对人类戒烟无影响:一项双盲、随机、安慰剂对照的临床研究。

Lack of effects of simvastatin on smoking cessation in humans: A double-blind, randomized, placebo-controlled clinical study.

机构信息

INSERM, Clinical Investigation Center CIC 1402, University of Poitiers, CHU Poitiers, Poitiers, France.

Department of Epidemiology & Biostatistics, Faculty of Medicine, Poitiers, France.

出版信息

Sci Rep. 2018 Mar 1;8(1):3836. doi: 10.1038/s41598-018-21819-7.

DOI:10.1038/s41598-018-21819-7
PMID:29497063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5832803/
Abstract

A recent pre-clinical study has shown that brain-penetrating statins can reduce risks of relapse to cocaine and nicotine addiction in rats. Based on this information, we conducted a randomized, double-blind, placebo-controlled, proof-of-concept trial to assess the efficacy of simvastatin in smoking cessation. After informed consent, 118 participants received behavioral cessation support and were randomly assigned to a 3-month treatment with simvastatin or placebo. The primary outcome was biochemically verified abstinence or smoking reduction at 3-month post-target quit date (TQD). Secondary outcomes were abstinence during weeks 9-12 post-TQD, prolonged abstinence or reduction at months 6 and 12 post-TQD, safety and craving assessed at each visit during the 3-month period of treatment. Simvastatin treatment was not associated with higher 3-month abstinence or smoking reduction compared to placebo. There was no significant difference in any of the secondary outcomes. Simvastatin was well tolerated. Over 3 and 9 months follow-up period, 78% simvastatin and 69% placebo participants were retained in the study. At 6 and 12 months, smoking remained significantly reduced from baseline in both groups. Our results demonstrate that a 3-month simvastatin treatment (40 mg/day), added to individual behavioral cessation support, does not improve significantly smoking cessation compared to placebo in humans.

摘要

一项最近的临床前研究表明,穿透血脑屏障的他汀类药物可以降低大鼠可卡因和尼古丁成瘾复发的风险。基于这一信息,我们进行了一项随机、双盲、安慰剂对照、概念验证试验,以评估辛伐他汀在戒烟中的疗效。在获得知情同意后,118 名参与者接受了行为戒烟支持,并被随机分配接受为期 3 个月的辛伐他汀或安慰剂治疗。主要结局是在目标戒烟日期(TQD)后 3 个月通过生物化学验证的戒烟或吸烟量减少。次要结局是在 TQD 后 9-12 周期间的戒烟、在 TQD 后 6 和 12 个月的延长戒烟或减少、在治疗期间的每个访视期间评估安全性和渴望。与安慰剂相比,辛伐他汀治疗与更高的 3 个月戒烟或吸烟减少无关。在任何次要结局中均无显著差异。辛伐他汀耐受性良好。在 3 个月和 9 个月的随访期间,分别有 78%的辛伐他汀和 69%的安慰剂参与者保留在研究中。在 6 个月和 12 个月时,两组的吸烟量均较基线显著减少。我们的结果表明,与安慰剂相比,在人类中,为期 3 个月的辛伐他汀治疗(40mg/天)联合个体化行为戒烟支持并不能显著提高戒烟率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/6fad9ae33d9f/41598_2018_21819_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/7fc3d3acf6d2/41598_2018_21819_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/4eb4e5860f1e/41598_2018_21819_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/84a67b252511/41598_2018_21819_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/6fad9ae33d9f/41598_2018_21819_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/7fc3d3acf6d2/41598_2018_21819_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/4eb4e5860f1e/41598_2018_21819_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/84a67b252511/41598_2018_21819_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ce/5832803/6fad9ae33d9f/41598_2018_21819_Fig4_HTML.jpg

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