Neural, psychological, and transcriptomic predictors of short video addiction: A multi-site longitudinal study of fear of missing out and negative affect

默认模式网络 纵向研究 心理学 转录组 神经科学 海马结构 静息状态功能磁共振成像 基因 发展心理学 情感(语言学) 兴奋性突触后电位 扁桃形结构 生物 功能连接 外围设备 认知 神经可塑性 意识的神经相关物 神经传递 心理化 临床心理学 海马体
作者
Chang Liu,Hanbing Li,Qianyi Shangguan,Yuyang Zeng,Pinchun Wang,Zhang Zong,Weipeng Jin,Qiang Wang
出处
期刊:NeuroImage [Elsevier BV]
卷期号:323: 121605-121605 被引量:2
标识
DOI:10.1016/j.neuroimage.2025.121605
摘要

Short video addiction symptoms (SVAS) have become increasingly prevalent, yet their longitudinal neurobiological basis remains unclear. In a multi-site longitudinal study (n = 280), we examined whether baseline brain features and dispositional traits-negative affect (NA) and fear of missing out (FoMO)-predict future SVAS. Participants completed self-report measures and MRI scans at baseline, with follow-up assessments conducted after 5 months to 5 years. Behaviorally, both baseline and follow-up NA and FoMO significantly predicted SVAS. Structurally, baseline gray matter volume (GMV) in the frontal-parietal network (FPN), default mode network (DMN), and hippocampal morphological patterns predicted follow-up SVAS severity. Functionally, baseline regional homogeneity (ReHo) in the FPN, DMN, ventral attention network (VAN), and sensorimotor network (SMN) also predicted SVAS. Parallel multiple mediation analyses revealed a dissociable neural architecture: hippocampal morphological patterns predicted SVAS via the unique indirect effect of follow-up FoMO, whereas DMN functional profiles (e.g., ReHo) predicted SVAS via follow-up NA. Notably, the VAN served as an integrative hub, exerting its influence via the unique indirect effects of both follow-up NA and FoMO. Transcriptomic analyses linked SVAS-related ReHo to two gene sets, namely positively correlated (SVAS-ReHo⁺) and negatively correlated (SVAS-ReHo⁻) genes. SVAS-ReHo⁺ genes were enriched in RNA processing and vascular signaling and expressed in endothelial cells; SVAS-ReHo⁻ genes were enriched in synaptic transmission and expressed in excitatory and inhibitory neurons. Spatial-temporal patterns showed SVAS-ReHo⁺ genes were expressed in subcortical regions across adolescence, whereas SVAS-ReHo⁻ genes were prominent in cortical-limbic areas during postnatal development. Functional decoding linked SVAS-ReHo⁺ genes to sensorimotor function and metabolism, and SVAS-ReHo⁻ genes to emotion and psychiatric risk. Together, these findings highlight dissociable structural, functional, and molecular pathways through which FoMO and NA contribute to short video addiction development.
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