The impact of anti-craving medication on cue reactivity and abstinence in patients undergoing alcohol detoxification: some preliminary evidence from a retrospective event-related potentials study.

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Clémence Dousset, Sonia Sistiaga, Anaïs Ingels, Catherine Hanak, Hendrik Kajosch, Salvatore Campanella
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引用次数: 0

Abstract

Rationale: While medications such as acamprosate, baclofen, or naltrexone have shown promising effects in the treatment of alcohol use disorder (AUD), meta-analyses have yielded conflicting findings regarding their efficacy. This retrospective study examined whether alcohol cue reactivity and its neural correlates could serve as protective factors against relapse in AUD inpatients receiving pharmacological treatment during a three-week detoxification program.

Method: Fifty-eight inpatients diagnosed with AUD undergoing a three-weeks detoxification program were selected. These patients received either acamprosate (n = 21), naltrexone (n = 21), or baclofen (n = 16) during their stay. They completed an event-related potential cue-reactivity task at the beginning (T0) and end (T1) of the program. Follow-up data on relapse were collected up to two months post- discharge.

Results: The Log-Rank (Mantel-Cox) test ([Formula: see text] (2) = 5.84; p =.059) revealed a marginally significant difference in survival distributions between medications. A significant difference emerged between baclofen and acamprosate groups ([Formula: see text] (1) = 4.73; p =.030), with slower return to alcohol use in the baclofen group. No other significant difference emerged between the acamprosate and naltrexone groups or between the naltrexone and baclofen groups (p >.05). Only the baclofen group showed a significant reduction in oddball P3 amplitude between T0 and T1 (p =.002), suggesting decreased neural cue reactivity.

Conclusion: A reduction in neural cue reactivity, observed exclusively in the baclofen group, may act as a protective factor against early relapse in AUD. However, this study was underpowered, and findings should be interpreted cautiously until confirmed in larger prospective investigations.

抗渴望药物对酒精解毒患者线索反应性和戒断的影响:来自回顾性事件相关电位研究的一些初步证据
理由:虽然阿坎普罗酸、巴氯芬或纳曲酮等药物在治疗酒精使用障碍(AUD)方面显示出有希望的效果,但荟萃分析得出的结果却相互矛盾。本回顾性研究探讨了酒精线索反应及其神经相关因素是否可作为在为期三周的戒毒计划中接受药物治疗的AUD住院患者复发的保护因素。方法:选择58例诊断为AUD的住院患者进行为期三周的戒毒计划。这些患者在住院期间接受了阿坎普罗酸(n = 21)、纳曲酮(n = 21)或巴氯芬(n = 16)治疗。他们在项目的开始(T0)和结束(T1)完成了一个与事件相关的潜在线索反应任务。复发的随访数据收集至出院后两个月。结果:Log-Rank (Mantel-Cox)检验([公式见文](2)= 5.84;P = 0.059)显示两种药物的生存分布差异有统计学意义。巴氯芬组和阿坎前列酯组之间存在显著差异([公式:见文](1)= 4.73;P = 0.030),巴氯芬组恢复饮酒的速度较慢。阿坎前列酯组和纳曲酮组之间、纳曲酮组和巴氯芬组之间没有其他显著差异(p < 0.05)。只有巴氯芬组在T0和T1之间显示奇异P3振幅显著降低(p = 0.002),提示神经线索反应性降低。结论:仅在巴氯芬组观察到的神经线索反应性降低可能是防止AUD早期复发的保护因素。然而,这项研究的力量不足,研究结果应谨慎解释,直到在更大的前瞻性调查中得到证实。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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