Dissociable neural processes during risky decision-making in individuals with Internet-gaming disorder

被引:43
作者
Liu, Lu [1 ]
Xue, Gui [2 ,3 ,4 ]
Potenza, Marc N. [5 ,6 ,7 ,8 ,9 ]
Zhang, Jin-Tao [2 ,3 ]
Yao, Yuan-Wei [2 ,3 ]
Xia, Cui-Cui [1 ,10 ]
Lan, Jing [1 ]
Ma, Shan-Shan [2 ,3 ]
Fang, Xiao-Yi [1 ]
机构
[1] Beijing Normal Univ, Inst Dev Psychol, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, State Key Lab Cognit Neurosci Learning, Beijing 100875, Peoples R China
[3] Beijing Normal Univ, IDG McGovern Inst Brain Res, Beijing 100875, Peoples R China
[4] Beijing Normal Univ, Ctr Collaborat & Innovat Brain & Learning Sci, Beijing 100875, Peoples R China
[5] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06519 USA
[6] Yale Univ, Sch Med, Dept Neurosci, New Haven, CT 06519 USA
[7] Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06519 USA
[8] Yale Univ, Sch Med, Natl Ctr Addict & Subst Abuse, New Haven, CT 06519 USA
[9] Connecticut Mental Hlth Ctr, 34 Pk St, New Haven, CT 06519 USA
[10] Beijing Normal Univ, Students Counseling Ctr, Beijing 100875, Peoples R China
基金
中国国家自然科学基金;
关键词
fMRI; Internet gaming disorder; Outcome processing; Risky decision-making; Risk evaluation; PREFRONTAL CORTEX; REWARD; ADDICTS; FMRI; NEUROBIOLOGY; UNCERTAINTY; INHIBITION; ACTIVATION; DEPENDENCE; INVENTORY;
D O I
10.1016/j.nicl.2017.03.010
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
Risk-taking is purported to be central to addictive behaviors. However, for Internet gaming disorder (IGD), a condition conceptualized as a behavioral addiction, the neural processes underlying impaired decision-making (risk evaluation and outcome processing) related to gains and losses have not been systematically investigated. Forty-one males with IGD and 27 healthy comparison (HC) male participants were recruited, and the cups task was used to identify neural processes associated with gain- and loss-related risk- and outcome-processing in IGD. During risk evaluation, the IGD group, compared to the HC participants, showed weaker modulation for experienced risk within the bilateral dorsolateral prefrontal cortex (DLPFC) (t = -4.07; t = -3.94; P-FWE < 0.05) and inferior parietal lobule (IPL) (t = -4.08; t = -4.08; P-FWE < 0.05) for potential losses. The modulation of the left DLPFC and bilateral IPL activation were negatively related to addiction severity within the IGD group (r = -0.55; r = -0.61; r = -0.51; P-FWE < 0.05). During outcome processing, the IGD group presented greater responses for the experienced reward within the ventral striatum, ventromedial prefrontal cortex, and orbitofrontal cortex (OFC) (t = 5.04, P-FWE < 0.05) for potential gains, as compared to HC participants. Within the IGD group, the increased reward-related activity in the right OFC was positively associated with severity of IGD (r = 0.51, P-FWE < 0.05). These results provide a neurobiological foundation for decision-making deficits in individuals with IGD and suggest an imbalance between hypersensitivity for reward and weaker risk experience and self-control for loss. The findings suggest a biological mechanism for why individuals with IGD may persist in game-seeking behavior despite negative consequences, and treatment development strategies may focus on targeting these neural pathways in this population.
引用
收藏
页码:741 / 749
页数:9
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