Abnormal Granger causal connectivity based on altered gray matter volume and associated neurotransmitters of adolescents with internet gaming disorder revealed by a multimodal neuroimaging study

IF 4.6 2区 医学 Q1 NEUROSCIENCES
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引用次数: 0

Abstract

Although prior studies have revealed alterations in gray matter volume (GMV) among individuals with internet gaming disorder (IGD). The brain's multifaceted functions hinge crucially on the intricate connections and communication among distinct regions. However, the intricate interaction of information between brain regions with altered GMV and other regions, and how they synchronize with various neurotransmitter systems, remains enigmatic. Therefore, we aimed to integrate structural, functional and molecular data to explore the GMV-based Granger causal connectivity abnormalities and their correlated neurotransmitter systems in IGD adolescents. Voxel-based morphometry (VBM) analysis was firstly performed to investigate GMV differences between 37 IGD adolescents and 35 matched controls. Brain regions with altered GMV were selected as seeds for further Granger causality analysis (GCA). Two-sample t tests were performed using the SPM12 toolkit to compare the GMV and Granger causal connectivity between IGD and control groups (GRF corrected, Pvoxel<0.005, Pcluster<0.05). Then, GMV-based Granger causal connectivity was spatially correlated with PET- and SPECT-derived maps covering multifarious neurotransmitter systems. Multiple comparison correction was performed using false discovery rate (FDR). Compared with controls, IGD adolescents showed higher GMV in the caudate nucleus and lingual gyrus. For the GCA, IGD adolescents showed higher Granger causal connectivity from insula, putamen, supplementary motor area (SMA) and middle cingulum cortex (MCC) to the caudate nucleus, and lower Granger causal connectivity from superior/inferior parietal gyrus (SPG/IPG) and middle occipital gyrus (MOG) to the lingual gyrus. Besides, GMV-based Granger causal connectivity of IGD adolescents were associated with the dopaminergic, serotonergic, GABAergic and noradrenaline systems. This study revealed that the caudate nucleus and lingual gyrus may be the key sites of neuroanatomical changes in IGD adolescents, and whole-brain Granger causal connectivity abnormalities based on altered GMV involved large brain networks including reward, cognitive control, and visual attention networks, and these abnormalities are associated with a variety of neurotransmitter systems, which may be associated with higher reward sensitivity, cognitive control, and attention control dysfunction.
多模态神经影像学研究发现,基于网络游戏障碍青少年灰质体积和相关神经递质改变的格兰杰因果连接异常
尽管先前的研究显示,网络游戏障碍(IGD)患者的灰质体积(GMV)发生了改变。大脑的多方面功能关键取决于不同区域之间错综复杂的联系和交流。然而,GMV改变的大脑区域与其他区域之间错综复杂的信息互动,以及它们如何与各种神经递质系统同步,仍然是个谜。因此,我们旨在整合结构、功能和分子数据,探索 IGD 青少年基于 GMV 的格兰杰因果连接异常及其相关神经递质系统。首先进行体素形态计量(VBM)分析,研究37名IGD青少年与35名匹配对照组之间的GMV差异。选取 GMV 发生变化的脑区作为种子区域,进一步进行格兰杰因果关系分析(GCA)。使用 SPM12 工具包进行双样本 t 检验,比较 IGD 组和对照组之间的 GMV 和格兰杰因果连通性(GRF 校正,Pvoxel<0.005,Pcluster<0.05)。然后,将基于 GMV 的格兰杰因果连通性与正电子发射计算机断层显像(PET)和正电子发射计算机断层显像(SPECT)得出的涵盖多种神经递质系统的图谱进行空间关联。使用错误发现率(FDR)进行多重比较校正。与对照组相比,IGD 青少年尾状核和舌回的 GMV 更高。在GCA方面,IGD青少年从岛叶、普塔门、辅助运动区(SMA)和中腔皮层(MCC)到尾状核的格兰杰因果连接性较高,而从顶上/顶下回(SPG/IPG)和枕中回(MOG)到舌回的格兰杰因果连接性较低。此外,IGD青少年基于GMV的格兰杰因果连通性与多巴胺能、血清素能、GABA能和去甲肾上腺素系统有关。该研究揭示,尾状核和舌回可能是IGD青少年神经解剖学变化的关键部位,基于GMV改变的全脑格兰杰因果连接异常涉及包括奖赏、认知控制和视觉注意力网络在内的大型脑网络,这些异常与多种神经递质系统有关,可能与奖赏敏感性增高、认知控制和注意力控制功能障碍有关。
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来源期刊
CiteScore
7.60
自引率
10.60%
发文量
124
审稿时长
6-12 weeks
期刊介绍: The journal publishes theoretical and research papers on cognitive brain development, from infancy through childhood and adolescence and into adulthood. It covers neurocognitive development and neurocognitive processing in both typical and atypical development, including social and affective aspects. Appropriate methodologies for the journal include, but are not limited to, functional neuroimaging (fMRI and MEG), electrophysiology (EEG and ERP), NIRS and transcranial magnetic stimulation, as well as other basic neuroscience approaches using cellular and animal models that directly address cognitive brain development, patient studies, case studies, post-mortem studies and pharmacological studies.
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