Roberts C A, Jones A, Montgomery C
Department of Psychological Sciences,University of Liverpool,Liverpool,UK.
School of Natural Sciences and Psychology, Liverpool John Moores University,Liverpool,UK.
Psychol Med. 2016 Jun;46(8):1581-96. doi: 10.1017/S0033291716000258. Epub 2016 Mar 11.
Ecstasy/3,4-methylenedioxymethamphetamine (MDMA) use is proposed to cause damage to serotonergic (5-HT) axons in humans. Therefore, users should show deficits in cognitive processes that rely on serotonin-rich, prefrontal areas of the brain. However, there is inconsistency in findings to support this hypothesis. The aim of the current study was to examine deficits in executive functioning in ecstasy users compared with controls using meta-analysis. We identified k = 39 studies, contributing 89 effect sizes, investigating executive functioning in ecstasy users and polydrug-using controls. We compared function-specific task performance in 1221 current ecstasy users and 1242 drug-using controls, from tasks tapping the executive functions - updating, switching, inhibition and access to long-term memory. The significant main effect demonstrated overall executive dysfunction in ecstasy users [standardized mean difference (SMD) = -0.18, 95% confidence interval (CI) -0.26 to -0.11, Z = 5.05, p < 0.001, I 2 = 82%], with a significant subgroup effect (χ 2 = 22.06, degrees of freedom = 3, p < 0.001, I 2 = 86.4%) demonstrating differential effects across executive functions. Ecstasy users showed significant performance deficits in access (SMD = -0.33, 95% CI -0.46 to -0.19, Z = 4.72, p < 0.001, I 2 = 74%), switching (SMD = -0.19, 95% CI -0.36 to -0.02, Z = 2.16, p < 0.05, I 2 = 85%) and updating (SMD = -0.26, 95% CI -0.37 to -0.15, Z = 4.49, p < 0.001, I 2 = 82%). No differences were observed in inhibitory control. We conclude that this is the most comprehensive analysis of executive function in ecstasy users to date and provides a behavioural correlate of potential serotonergic neurotoxicity.
摇头丸/3,4-亚甲基二氧甲基苯丙胺(MDMA)的使用被认为会对人类的5-羟色胺能(5-HT)轴突造成损害。因此,使用者在依赖大脑富含血清素的前额叶区域的认知过程中应表现出缺陷。然而,研究结果并不一致,无法支持这一假设。本研究的目的是通过荟萃分析,研究摇头丸使用者与对照组相比在执行功能方面的缺陷。我们确定了39项研究,提供了89个效应量,调查了摇头丸使用者和多药滥用对照组的执行功能。我们比较了1221名当前摇头丸使用者和1242名药物滥用对照组在特定功能任务上的表现,这些任务涉及执行功能——更新、转换、抑制和长期记忆提取。显著的主效应表明摇头丸使用者总体存在执行功能障碍[标准化均数差(SMD)=-0.18,95%置信区间(CI)-0.26至-0.11,Z=5.05,p<0.001,I²=82%],存在显著的亚组效应(χ²=22.06,自由度=3,p<0.001,I²=86.4%),表明执行功能之间存在差异效应。摇头丸使用者在提取(SMD=-0.33,95%CI-0.46至-0.19,Z=4.72,p<0.001,I²=74%)、转换(SMD=-0.19,95%CI-0.36至-0.02,Z=2.16,p<0.05,I²=85%)和更新(SMD=-0.26,95%CI-0.37至-0.15,Z=4.49,p<0.001,I²=82%)方面表现出显著的表现缺陷。在抑制控制方面未观察到差异。我们得出结论认为,这是迄今为止对摇头丸使用者执行功能最全面的分析,并提供了潜在的5-羟色胺能神经毒性的行为关联。