Kashif Saima, Pandey Samiksha, Warriach Zain I
Department of Research, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Department of Research, Division of Clinical & Translational Research/Larkin Health System, Miami, USA.
Cureus. 2021 Sep 10;13(9):e17866. doi: 10.7759/cureus.17866. eCollection 2021 Sep.
Pathological online gaming is a relatively newer psychiatric disorder. It is the second behavioral addiction (after internet gambling disorder) included in the Diagnostic and Statistical Manual of Psychiatric Disorders (DSM), 5 edition as "Internet Gaming Disorder" (IGD). Recent research is showing high morbidity associated with IGD, thus encouraging researchers to find valid and reliable biomarkers of IGD. So that, early diagnosis and proper treatment could limit the high disability level accompanying excessive online gaming. As electroencephalography (EEG) is a non-invasive and relatively easily available diagnostic technique, we aimed at collecting EEG studies that investigated EEG changes associated with IGD, with a specific focus on finding diagnostic and predictive neurophysiological biomarkers of IGD. We searched PubMed and Google Scholar for EEG studies of IGD. We eliminated those EEG studies that were not focused on finding biomarkers. Scale for the Assessment of Narrative Review Articles (SANRA) is followed in the writing of this review article. Our results showed that increased slow-wave resting-state activity and reduced P300 and N100 can serve as useful IGD diagnostic markers of IGD. Moreover, increased resting-state theta activity can be a predictive biomarker of IGD. Lastly, increased late low potentials (LLPs) can be specific trait markers of cue-induced cravings in IGD.
病理性网络游戏是一种相对较新的精神障碍。它是《精神疾病诊断与统计手册》(DSM)第5版中作为“互联网游戏障碍”(IGD)纳入的第二种行为成瘾(仅次于网络赌博障碍)。最近的研究表明IGD的发病率很高,这促使研究人员寻找有效且可靠的IGD生物标志物。这样,早期诊断和适当治疗可以限制过度网络游戏所伴随的高残疾水平。由于脑电图(EEG)是一种非侵入性且相对容易获得的诊断技术,我们旨在收集研究IGD相关脑电图变化的EEG研究,特别关注寻找IGD的诊断和预测性神经生理生物标志物。我们在PubMed和谷歌学术上搜索了关于IGD的EEG研究。我们排除了那些并非专注于寻找生物标志物的EEG研究。本综述文章的撰写遵循叙事性综述文章评估量表(SANRA)。我们的结果表明,静息状态下慢波活动增加以及P300和N100降低可作为IGD有用的诊断标志物。此外,静息状态下θ活动增加可能是IGD的预测性生物标志物。最后,晚期低电位(LLP)增加可能是IGD中线索诱发渴望的特定特质标志物。