Brower Kirk J, Myra Kim Hyungjin, Strobbe Stephen, Karam-Hage Maher A, Consens Flavia, Zucker Robert A
University of Michigan Addiction Research Center, 4250 Plymouth Road, Ann Arbor, MI 48109-5740, USA.
Alcohol Clin Exp Res. 2008 Aug;32(8):1429-38. doi: 10.1111/j.1530-0277.2008.00706.x. Epub 2008 Jun 6.
Insomnia and other sleep disturbances are common, persistent, and associated with relapse in alcohol-dependent patients. The purpose of this pilot study was to compare gabapentin versus placebo for the treatment of insomnia and prevention of relapse in alcohol-dependent patients.
Twenty-one subjects, including 10 women who met study criteria for alcohol dependence and insomnia and expressed a desire to abstain from alcohol, were recruited to the study. During a 1 to 2 week placebo lead-in and screening phase, a complete medical history, physical exam, blood tests, urine drug test, and structured interviews were performed to determine eligibility and patterns of alcohol use and sleep. Insomnia due to intoxication or acute withdrawal, psychiatric or medical illness, medications, and other sleep disorders were ruled out. Subjects were then randomized to either placebo (n = 11) or gabapentin (n = 10) for 6 weeks and titrated over a 10-day period to 1,500 mg or 5 pills at bedtime. After a 4-day taper, subjects were reassessed 6 weeks after ending treatment.
Gabapentin significantly delayed the onset to heavy drinking, an effect which persisted for 6 weeks after treatment ended. Insomnia improved in both treatment groups during the medication phase, but gabapentin had no differential effects on sleep as measured by either subjective report or polysomnography.
Because gabapentin is a short-acting medication that was taken only at nighttime in this study, it may possibly exert a nocturnal effect that prevents relapse to heavy drinking by a physiological mechanism not measured in this pilot study.
失眠及其他睡眠障碍在酒精依赖患者中很常见、持续存在且与复发相关。本初步研究的目的是比较加巴喷丁与安慰剂治疗酒精依赖患者失眠及预防复发的效果。
招募了21名受试者,其中包括10名符合酒精依赖和失眠研究标准且表示希望戒酒的女性。在为期1至2周的安慰剂导入和筛查阶段,进行了完整的病史、体格检查、血液检查、尿液药物检测及结构化访谈,以确定入选资格以及酒精使用和睡眠模式。排除了由中毒或急性戒断、精神或躯体疾病、药物及其他睡眠障碍引起的失眠。然后将受试者随机分为安慰剂组(n = 11)或加巴喷丁组(n = 10),为期6周,并在10天内滴定至睡前1500毫克或5片。经过4天的逐渐减量后,在治疗结束6周后对受试者进行重新评估。
加巴喷丁显著延迟了大量饮酒的开始时间,该效果在治疗结束后持续了6周。在用药阶段,两个治疗组的失眠情况均有所改善,但通过主观报告或多导睡眠图测量,加巴喷丁对睡眠没有差异影响。
由于加巴喷丁是一种短效药物,且在本研究中仅在夜间服用,它可能通过一种本初步研究未测量的生理机制产生夜间效应,从而防止复发至大量饮酒。