Prisciandaro James J, Hoffman Michaela, Brown Truman R, Voronin Konstantin, Book Sarah, Bristol Emily, Anton Raymond F
Department of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Am J Psychiatry. 2021 Sep 1;178(9):829-837. doi: 10.1176/appi.ajp.2021.20121757. Epub 2021 Jul 14.
Although gabapentin has demonstrated efficacy in mitigating alcohol withdrawal symptoms and preventing relapse drinking in individuals with alcohol use disorder (AUD), the neurobiological mechanisms of action underlying these therapeutic effects remain unknown. The present study evaluated changes in GABA and glutamate levels in the dorsal anterior cingulate cortex (dACC) as candidate mechanisms of action.
In a 16-week randomized clinical trial, 68 adults with AUD, including a history of alcohol withdrawal syndrome, received 1,200 mg/day of gabapentin (N=37) or placebo (N=31) and nine medical management visits after ≥72 hours of abstinence. Proton MR spectroscopy (H-MRS) estimates of dACC levels of GABA (N=67) and glutamate (N=64) were acquired before start of treatment and again approximately 14 days after randomization. Percent days abstinent was reported via timeline followback interview.
The effects of gabapentin on GABA and glutamate levels were significantly associated with participants' percent days abstinent during early treatment. Specifically, gabapentin was associated with greater increases in glutamate and greater decreases in GABA levels in participants who remained mostly or entirely abstinent, and yet the opposite in participants who drank on more than half of the days preceding the second scan. Furthermore, gabapentin-treated participants with greater increases in glutamate levels during early treatment had significantly more percent days abstinent across the remainder of the study, relative to placebo-treated participants.
In addition to providing insight into the mechanisms through which gabapentin may promote abstinence in individuals with AUD, this study also provides evidence for a biomarker of efficacious treatment that may be used to evaluate other glutamatergic or GABAergic medications for AUD and related conditions.
尽管加巴喷丁已被证明在减轻酒精使用障碍(AUD)患者的酒精戒断症状和预防复饮方面具有疗效,但其这些治疗效果背后的神经生物学作用机制仍不清楚。本研究评估了背侧前扣带回皮质(dACC)中γ-氨基丁酸(GABA)和谷氨酸水平的变化,将其作为可能的作用机制。
在一项为期16周的随机临床试验中,68名患有AUD且有酒精戒断综合征病史的成年人,在戒酒≥72小时后,接受1200毫克/天的加巴喷丁(N = 37)或安慰剂(N = 31)治疗,并进行9次医疗管理随访。在治疗开始前以及随机分组后约14天再次采集dACC中GABA(N = 67)和谷氨酸(N = 64)水平的质子磁共振波谱(H-MRS)估计值。通过时间线回溯访谈报告戒酒天数百分比。
加巴喷丁对GABA和谷氨酸水平的影响与早期治疗期间参与者的戒酒天数百分比显著相关。具体而言,在大部分或完全戒酒的参与者中,加巴喷丁与谷氨酸水平的更大升高和GABA水平的更大降低相关,而在第二次扫描前超过一半天数饮酒的参与者中则相反。此外,与接受安慰剂治疗的参与者相比,在早期治疗期间谷氨酸水平升高幅度更大的加巴喷丁治疗参与者在研究的其余时间内戒酒天数百分比显著更高。
除了深入了解加巴喷丁可能促进AUD患者戒酒的机制外,本研究还为有效治疗的生物标志物提供了证据,该生物标志物可用于评估其他用于AUD及相关病症的谷氨酸能或GABA能药物。