Frontostriatal circuits, resting state functional connectivity and cognitive control in internet gaming disorder

斯特罗普效应 神经科学 心理学 伏隔核 腹侧纹状体 眶额皮质 静息状态功能磁共振成像 纹状体 认知 前额叶皮质 神经影像学 免疫球蛋白D 扣带回前部 尾状核 医学 中枢神经系统 多巴胺 B细胞 免疫学 抗体
作者
Kai Yuan,Dahua Yu,Chenxi Cai,Dan Feng,Yangding Li,Yanzhi Bi,Jixin Liu,Yi Zhang,Chenwang Jin,Linling Li,Wei Qin,Jie Tian
出处
期刊:Addiction Biology [Wiley]
卷期号:22 (3): 813-822 被引量:140
标识
DOI:10.1111/adb.12348
摘要

Converging evidence has identified cognitive control deficits in internet gaming disorder (IGD). Recently, mounting evidence had revealed that resting state functional connectivity (RSFC) and structural connectivity of frontostriatal circuits could modulate cognitive control in healthy individuals. Unfortunately, relatively little is known about the thoroughly circuit-level characterization of the frontostriatal pathways (both the dorsal and ventral striatum) during resting-state and their association with cognitive control in IGD. In the current study, the differences of striatum volume and RSFC networks were investigated between 43 young IGD individuals and 44 healthy controls. Meanwhile, cognitive control deficits were assessed by Stroop task performances. The neuroimaging findings were then correlated with the Stroop task behaviors. In IGD subjects, we demonstrated an increased volume of right caudate and nucleus accumbens (NAc) as well as reduced RSFC strength of dorsal prefrontal cortex (DLPFC)-caudate and orbitofrontal cortex (OFC)-NAc. NAc volumes were positively correlated with internet addiction test scores in IGD. The caudate volume and DLPFC-caudate RSFC was correlated with the impaired cognitive control (more incongruent errors in Stroop task) in IGD. Consistent with substance use disorder (SUD) findings, we detected striatum volume and frontostriatal circuits RSFC differences between IGD and healthy controls, which provided evidence of some degree of the similarity between IGD and SUD. More importantly, the cognitive control deficits in IGD were correlated with the reduced frontostrital RSFC strength. It is hoped that our results could shed insight on the neurobiological mechanisms of IGD and suggest potential novel therapeutic targets for treatment.
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