Suppr超能文献

加巴喷丁恩卡他必利缓释片治疗酒精使用障碍的随机、双盲、安慰剂对照、多中心试验:评估疗效和安全性。

Gabapentin Enacarbil Extended-Release for Alcohol Use Disorder: A Randomized, Double-Blind, Placebo-Controlled, Multisite Trial Assessing Efficacy and Safety.

机构信息

National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland.

Department of Psychiatry, Boston University School of Medicine, Boston, Massachusetts.

出版信息

Alcohol Clin Exp Res. 2019 Jan;43(1):158-169. doi: 10.1111/acer.13917. Epub 2018 Dec 9.

Abstract

BACKGROUND

Several single-site alcohol treatment clinical trials have demonstrated efficacy for immediate-release (IR) gabapentin in reducing drinking outcomes among individuals with alcohol dependence. The purpose of this study was to conduct a large, multisite clinical trial of gabapentin enacarbil extended-release (GE-XR) (HORIZANT ), a gabapentin prodrug formulation, to determine its safety and efficacy in treating alcohol use disorder (AUD).

METHODS

Men and women (n = 346) who met DSM-5 criteria for at least moderate AUD were recruited across 10 U.S. clinical sites. Participants received double-blind GE-XR (600 mg twice a day) or placebo and a computerized behavioral intervention (Take Control) for 6 months. Efficacy analyses were prespecified for the last 4 weeks of the treatment period.

RESULTS

The GE-XR and placebo groups did not differ significantly on the primary outcome measure, percentage of subjects with no heavy drinking days (28.3 vs. 21.5, respectively, p = 0.157). Similarly, no clinical benefit was found for other drinking measures (percent subjects abstinent, percent days abstinent, percent heavy drinking days, drinks per week, drinks per drinking day), alcohol craving, alcohol-related consequences, sleep problems, smoking, and depression/anxiety symptoms. Common side-effects were fatigue, dizziness, and somnolence. A population pharmacokinetics analysis revealed that patients had lower gabapentin exposure levels compared with those in other studies using a similar dose but for other indications.

CONCLUSIONS

Overall, GE-XR at 600 mg twice a day did not reduce alcohol consumption or craving in individuals with AUD. It is possible that, unlike the IR formulation of gabapentin, which showed efficacy in smaller Phase 2 trials at a higher dose, GE-XR is not effective in treating AUD, at least not at doses approved by the U.S. Food and Drug Administration for treating other medical conditions.

摘要

背景

几项单部位酒精治疗临床试验表明,即时释放(IR)加巴喷丁在减少酒精依赖个体的饮酒结果方面具有疗效。本研究的目的是对加巴喷丁前体药物制剂加巴喷丁恩卡他比缓释片(HORIZANT)进行一项大型、多部位的临床研究,以确定其治疗酒精使用障碍(AUD)的安全性和疗效。

方法

符合 DSM-5 至少中度 AUD 标准的男性和女性(n=346)在美国 10 个临床地点招募。参与者接受为期 6 个月的双盲加巴喷丁恩卡他比缓释片(600mg,每日两次)或安慰剂和计算机化行为干预(Take Control)治疗。疗效分析预先设定在治疗期的最后 4 周。

结果

加巴喷丁恩卡他比缓释片组和安慰剂组在主要结局测量(无重度饮酒天数的受试者百分比)上无显著差异(分别为 28.3%和 21.5%,p=0.157)。同样,其他饮酒测量(戒酒的受试者百分比、戒酒的天数百分比、重度饮酒天数百分比、每周饮酒量、每日饮酒量)、酒精渴求、酒精相关后果、睡眠问题、吸烟和抑郁/焦虑症状也未发现临床获益。常见的副作用是疲劳、头晕和嗜睡。群体药代动力学分析显示,与其他使用类似剂量但用于其他适应症的研究相比,患者的加巴喷丁暴露水平较低。

结论

总的来说,每日两次 600mg 的加巴喷丁恩卡他比缓释片并不能减少 AUD 患者的饮酒量或渴求。与在较小的 2 期试验中以更高剂量显示疗效的 IR 加巴喷丁制剂不同,加巴喷丁恩卡他比缓释片可能对 AUD 无效,至少在美国食品和药物管理局批准用于治疗其他医疗状况的剂量下无效。

相似文献

7
Gabapentin enacarbil in restless legs syndrome.加巴喷丁依卡倍特治疗不宁腿综合征
Drugs Today (Barc). 2010 Jan;46(1):3-11. doi: 10.1358/dot.2010.46.1.1424766.

引用本文的文献

本文引用的文献

1
Gabapentin for the treatment of alcohol use disorder.加巴喷丁用于治疗酒精使用障碍。
Expert Opin Investig Drugs. 2018 Jan;27(1):113-124. doi: 10.1080/13543784.2018.1417383. Epub 2017 Dec 23.
6
Gabapentin: Abuse, Dependence, and Withdrawal.加巴喷丁:滥用、依赖与戒断反应
Ann Pharmacother. 2016 Mar;50(3):229-33. doi: 10.1177/1060028015620800. Epub 2015 Dec 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验