Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
Psychiatry Service, VA Connecticut Healthcare System, West Haven, Connecticut, USA.
Subst Abus. 2021;42(4):412-416. doi: 10.1080/08897077.2020.1844847. Epub 2020 Dec 7.
Pharmacological and psychosocial interventions have only modest efficacy for Alcohol Use Disorder (AUD), and continued alcohol use has brain effects on neurocognition, which place heavy drinkers at increased risk of early onset dementia. The most common neurocognitive deficits are in the domains of executive function and memory, and these deficits may impact AUD treatment outcomes. AUD related Mild Cognitive Impairment (AUD-MCI) is a diagnosis in DSM-V and ICD-10. Donepezil, a cholinesterase inhibitor, is currently FDA approved for treatment of dementia, and recent preclinical research suggests anticholinesterase agents may treat alcoholism. Another approach to cognitive recovery is Cognitive Remediation Therapy (CRT). Recent research supports CRT efficacy in schizophrenia and related disorders, and some research suggests that CRT could improve neurocognition in substance abuse disorders (SUDs). This is the first report of an open-label clinical trial that combined donepezil with CRT to improve neurocognitive and clinical outcomes in the early phase of AUD recovery. Eleven older male US Veterans with AUD-MCI as determined by Level II neurocognitive criteria and who had recently relapsed participated in an open-label trial of 13 weeks of donepezil combined with CRT. They were compared with matched historical control samples on neurocognitive and clinical outcomes. Participants had excellent adherence to donepezil and CRT. Neurocognitive improvements were highly significant on a composite score of learning and memory and executive function measures ( < .0001) and was significantly better than historical matched controls ( < .001). On a Clinical Global Impression scale, 90.9% of participants had a good clinical recovery compared with 59.5% of historical matched controls ( <.052). AUD-MCI has not received much research attention but is of considerable public health importance. Findings in this open-label trial of donepezil + CRT should encourage further investigation into the clinical benefit of this combined treatment for AUD-MCI.
药物和心理社会干预措施对酒精使用障碍(AUD)仅有适度疗效,持续饮酒对神经认知有大脑影响,这使重度饮酒者有更高的早发性痴呆风险。最常见的神经认知缺陷是在执行功能和记忆领域,这些缺陷可能会影响 AUD 治疗效果。AUD 相关轻度认知障碍(AUD-MCI)是 DSM-V 和 ICD-10 中的诊断。多奈哌齐是一种乙酰胆碱酯酶抑制剂,目前已获得 FDA 批准用于治疗痴呆症,最近的临床前研究表明,抗胆碱酯酶药物可能治疗酒精中毒。认知康复治疗(CRT)是另一种认知恢复方法。最近的研究支持 CRT 在精神分裂症和相关障碍中的疗效,一些研究表明 CRT 可以改善物质使用障碍(SUDs)的神经认知。这是第一个报告联合多奈哌齐和 CRT 改善 AUD 恢复早期阶段神经认知和临床结果的开放性临床试验。11 名年龄较大的美国男性退伍军人,根据二级神经认知标准确定患有 AUD-MCI,并且最近复发,参加了为期 13 周的多奈哌齐联合 CRT 开放性试验。他们与匹配的历史对照样本在神经认知和临床结果上进行了比较。参与者对多奈哌齐和 CRT 的依从性极好。学习和记忆以及执行功能测量的综合评分上的神经认知改善具有高度显著性(<0.0001),明显优于历史匹配对照组(<0.001)。在临床总体印象量表上,90.9%的参与者与历史匹配对照组(<0.052)的 59.5%相比有良好的临床恢复。AUD-MCI 没有得到太多研究关注,但具有相当大的公共卫生重要性。这项多奈哌齐+CRT 开放性试验的结果应该鼓励进一步研究这种联合治疗对 AUD-MCI 的临床益处。