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安非他命和相关精神兴奋剂对冲动性的急性影响:临床试验的系统评价。

Acute effects of amphetamine and related psychostimulants on impulsivity: a systematic review of clinical trials.

机构信息

Centre for Human Psychopharmacology, Swinburne University of Technology, Melbourne, Victoria, Australia.

Institute for Breathing and Sleep, Austin Hospital, Melbourne, Victoria, Australia.

出版信息

Addict Biol. 2022 Mar;27(2):e13128. doi: 10.1111/adb.13128.

Abstract

Evidence for acute amphetamine effects on behavioural impulsivity in healthy populations remains elusive and, at times, mixed. This review collates and reviews the clinical literature on the acute effects of amphetamines on measures of behavioural impulsivity in healthy adults. Randomised and placebo-controlled clinical trials that assessed behavioural impulsivity following the administration of an acute dose of amphetamine or a related psychostimulant (including amphetamine analogues and methylphenidate) were eligible for inclusion. The EBSCOHost, SCOPUS, PsychNet, Web of Science and ProQuest databases were searched from inception to 26 April 2021. Study selection, data extraction and the Cochrane risk of bias assessments were conducted by two independent reviewers. Reporting follows PRISMA guidelines, and the review was registered a priori on the PROSPERO database (Registration No: CRD42021249861). A total of 20 studies were included, comprising a total of 737 participants. Overall, results indicate that low-moderate doses of amphetamine and related psychostimulants may improve (i.e., reduce) impulsive responding without compromising performance, reflecting enhanced inhibitory control of behaviour. These effects are mild and appear most pronounced in individuals with high baseline impulsivity. This review highlights the need for greater consistency in behavioural task selection and future high-quality and well-designed studies to address current concerns around growing prescription psychostimulant use and misuse.

摘要

在健康人群中,急性安非他命对行为冲动的影响的证据仍然难以捉摸,有时甚至相互矛盾。这篇综述汇集并回顾了关于健康成年人急性安非他命对行为冲动测量影响的临床文献。符合纳入标准的研究为随机和安慰剂对照临床试验,评估了急性安非他命或相关精神兴奋剂(包括安非他命类似物和哌甲酯)给药后对行为冲动的影响。从研究开始到 2021 年 4 月 26 日,我们在 EBSCOHost、SCOPUS、PsychNet、Web of Science 和 ProQuest 数据库中进行了搜索。两名独立评审员进行了研究选择、数据提取和 Cochrane 偏倚风险评估。报告遵循 PRISMA 指南,该综述已在 PROSPERO 数据库(注册号:CRD42021249861)中预先注册。共纳入 20 项研究,共 737 名参与者。总体而言,结果表明,低至中等剂量的安非他命和相关精神兴奋剂可能会改善(即减少)冲动反应而不影响表现,这反映了行为的抑制控制得到增强。这些影响很轻微,在基线冲动性较高的个体中最为明显。该综述强调需要在行为任务选择方面更加一致,并开展更多高质量和精心设计的研究,以解决当前对处方精神兴奋剂使用和滥用日益增加的关注。

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