Department of Neurosciences, Institute for Functional Genomics, INSERM U-661, CNRS UMR-5203, 34094 Montpellier, France.
INSERM 1114, Department of Psychiatry and Addictology, University Hospital of Strasbourg, Fédération de Médecine Translationnelle de Strasbourg (FMTS), 67000 Strasbourg, France.
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Feb 2;81:306-332. doi: 10.1016/j.pnpbp.2017.09.008. Epub 2017 Sep 14.
Alcohol, tobacco, and illegal drug usage is pervasive throughout the world, and abuse of these substances is a major contributor to the global disease burden. Many pharmacotherapies have been developed over the last 50years to target addictive disorders. While the efficacy of these pharmacotherapies is largely recognized, their cognitive impact is less known. However, all substance abuse disorders are known to promote cognitive disorders like executive dysfunction and memory impairment. These impairments are critical for the maintenance of addictive behaviors and impede cognitive behavioral therapies that are regularly administered in association with pharmacotherapies. It is also unknown if addictolytic medications have an impact on preexisting cognitive disorders, and if this impact is modulated by the indication of prescription, i.e. abstinence, reduction or substitution, or by the specific action of the medication.
We reviewed the cognitive effects of labeled medications for tobacco addiction (varenicline, bupropion, nicotine patch and nicotine gums), alcohol addiction (naltrexone, nalmefene, baclofen, disulfiram, sodium oxybate, acamprosate), and opioid addiction (methadone, buprenorphine) in human studies. Studies were selected following MOOSE guidelines for systematic reviews of observational studies, using the keywords [Cognition] and [Cognitive disorders] and [treatment] for each medication.
971 articles were screened and 77 studies met the inclusion criteria and were reported in this review (for alcohol abuse, n=21, for tobacco n=22, for opioid n=34. However, very few comparative clinical trials have explored the chronic effects of addictolytic medications on cognition in addictive behaviors, and there are no clinical trials on the cognitive impact of nalmefene in patients suffering from alcohol use disorders.
Although some medications seem to enhance cognition in patients suffering from cognitive disorders, others could promote cognitive impairments, and our work highlights a lack of literature on this subject. In conclusion, more comparative clinical trials are needed to better understand the cognitive impact of addictolytic medications.
酒精、烟草和非法药物的使用在全球范围内普遍存在,这些物质的滥用是全球疾病负担的主要原因之一。在过去的 50 年中,已经开发出许多药物疗法来针对成瘾障碍。尽管这些药物疗法的疗效已得到广泛认可,但它们对认知的影响却知之甚少。然而,所有物质滥用障碍都已知会导致认知障碍,如执行功能障碍和记忆障碍。这些损伤对于维持成瘾行为至关重要,并阻碍了与药物治疗相结合的认知行为疗法。目前尚不清楚戒毒药物是否会对先前存在的认知障碍产生影响,如果有影响,这种影响是否会因处方的适应症(即戒断、减少或替代)或药物的具体作用而有所不同。
我们回顾了标签药物治疗烟草成瘾(伐伦克林、安非他酮、尼古丁贴片和尼古丁咀嚼剂)、酒精成瘾(纳曲酮、纳美芬、巴氯芬、双硫仑、羟丁酸钠、阿坎酸)和阿片类药物成瘾(美沙酮、丁丙诺啡)的认知效应。使用每个药物的关键字[认知]和[认知障碍]和[治疗],按照 MOOSE 指南对观察性研究进行系统综述,筛选了 971 篇文章,77 项研究符合纳入标准,并在本综述中报告(酒精滥用 n=21,烟草 n=22,阿片类药物 n=34。然而,很少有比较性临床试验探索戒毒药物对成瘾行为中认知的慢性影响,也没有关于纳美芬在酒精使用障碍患者中认知影响的临床试验。
尽管一些药物似乎可以提高认知障碍患者的认知能力,但其他药物可能会导致认知损伤,我们的工作强调了这方面文献的缺乏。总之,需要更多的比较性临床试验来更好地了解戒毒药物对认知的影响。