Ji Sun Kim, Young Wook Song, Sungkean Kim, Ji-Yoon Lee, So Young Yoo, Joon Hwan Jang, Jung-Seok Choi
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引用次数: 0
Abstract
Introduction: To investigate the neurophysiological aspects of addiction, the microstate characteristics of internet gaming disorder (IGD), alcohol use disorder (AUD), and healthy control (HC) groups were compared using resting-state electroencephalography (EEG).
Methods: In total, 199 young adults (75 patients with IGD, 57 patients with AUD, and 67 HCs) participated in this study. We conducted EEG microstate analysis among the groups and also compared the obtained parameters with the results of psychological assessments.
Results: The global explained variance, occurrence, and coverage of microstate C were significantly lower in the AUD group than in the IGD group. Additionally, rates of transition from microstates A, B, and D to C were significantly lower in the AUD group than in the IGD group, whereas rates of transition from microstate A to B were lower in the IGD group compared to HCs. Furthermore, the occurrence of microstate C and transition from microstate B to C were negatively correlated with the Alcohol Use Disorder Identification and Behavioural Inhibition Scale score.
Conclusion: There were significant differences in microstate characteristics among the groups, which correlated with the psychological scores. These findings suggest that microstate features can be used as neuromarkers in clinical settings to differentiate between addictive disorders and evaluate the pathophysiology of AUD and IGD.
简介为了研究成瘾的神经生理学方面,我们使用静息状态脑电图(EEG)比较了网络游戏障碍(IGD)、酒精使用障碍(AUD)和健康对照组(HC)的微观状态特征:共有 199 名年轻成人(75 名 IGD 患者、57 名 AUD 患者和 67 名 HC)参与了本研究。我们对各组进行了脑电图微状态分析,并将获得的参数与心理评估结果进行了比较:结果:AUD 组微态 C 的总体解释方差、发生率和覆盖率明显低于 IGD 组。此外,AUD 组从微状态 A、B 和 D 过渡到 C 的比率明显低于 IGD 组,而 IGD 组从微状态 A 过渡到 B 的比率低于 HC 组。此外,微状态 C 的出现以及从微状态 B 到 C 的转变与酒精使用障碍识别和行为抑制量表的评分呈负相关:结论:各组间的微状态特征存在明显差异,并与心理评分相关。这些研究结果表明,微状态特征可作为神经标记物用于临床环境,以区分成瘾性疾病并评估 AUD 和 IGD 的病理生理学。
期刊介绍:
Dialogues in Clinical Neuroscience (DCNS) endeavors to bridge the gap between clinical neuropsychiatry and the neurosciences by offering state-of-the-art information and original insights into pertinent clinical, biological, and therapeutic aspects. As an open access journal, DCNS ensures accessibility to its content for all interested parties. Each issue is curated to include expert reviews, original articles, and brief reports, carefully selected to offer a comprehensive understanding of the evolving landscape in clinical neuroscience. Join us in advancing knowledge and fostering dialogue in this dynamic field.