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社交焦虑症状与脑代谢的相关性研究

Association Between Social Anxiety Symptoms and Brain Metabolism

  • 摘要:
    目的 运用18氟(18F)-代脱氧葡萄糖(flurodeoxyglucose, FDG)正电子发射断层成像/计算机断层扫描(positron emission tomography/computed tomography, PET/CT)技术,分析利博维茨社交焦虑量表(Liebowitz Social Anxiety Scale, LSAS)不同量表模型与脑区代谢的相关性,以揭示社交焦虑的神经生物学基础。
    方法 共招募39名认知正常的受试者(男性29例,女性10例,年龄范围30~63岁),对其进行LSAS评估及脑18F-FDG PET扫描,进而分析脑区代谢与LSAS各模型评分之间的相关性。
    结果 结果显示,LSAS分量表得分与特定脑区的代谢活动之间存在统计学意义的关联。在Safren模型中,他人观察分量表得分与左侧梭状回(P<0.001,FDR校正)及左侧尾状核尾部(P<0.001,FDR校正)呈正相关,提示与他人观察相关的情绪状态与上述脑区的代谢活动密切相关。在Baker模型中,进食和饮水分量表得分与右侧楔前叶(P<0.001,FDR校正)呈负相关,而自我主张分量表得分与左侧尾状核(P<0.001,FDR校正)呈正相关。这些结果揭示了不同情绪和行为维度与特定脑区代谢活动之间复杂的关联模式。
    结论 社交焦虑与特定脑区(包括左侧岛叶、左侧尾状核尾部及右侧楔前叶)的代谢变化密切相关,且不同社交情境所激活的脑区存在差异。与社交焦虑障碍患者相比,正常人群的社交焦虑涉及脑区较少。本研究为理解社交焦虑的神经机制提供了新的实验证据。

     

    Abstract:
    Objective In this study, we investigated the correlation between the scores for different Liebowitz Social Anxiety Scale (LSAS) subscale models and the metabolic activity in specific regions of the brain using 18F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) (18F-FDG PET), thereby improving the understanding of the neurobiological characteristics of social anxiety.
    Methods A total of 39 cognitively normal participants (29 men and 10 women, aged 30-63 years) were enrolled. All participants underwent LSAS assessment and brain 18F-FDG PET scanning. Correlations between metabolic activities in various brain regions and scores from the different LSAS subscales were analyzed accordingly.
    Results LSAS subscale scores were significantly correlated with metabolic activity in specific brain regions. In the Safren model, the score for the observation by others subscale was positively correlated with the left fusiform gyrus (P < 0.001, false discovery rate FDR-corrected) and the left caudate tail (P < 0.001, FDR-corrected), suggesting a close association between mood states related to observation by others and the metabolic activity in these regions. In the Baker model, the score for the eating and drinking subscale was negatively correlated with the right precuneus (P < 0.001, FDR-corrected), while the score for the assertiveness subscale was positively correlated with the left caudate nucleus (P < 0.001, FDR-corrected). These findings revealed the complex associative patterns between various mood and behavioral dimensions and metabolic activities in specific brain regions.
    Conclusion Social anxiety symptoms are closely associated with metabolic changes in specific brain regions, including the left insula, left caudate tail, and right precuneus. Moreover, different social situations activate distinct brain regions. Compared with individuals with social anxiety disorder, normal individuals exhibit involvement of fewer brain regions when experiencing social anxiety. These findings provide new experimental evidence for understanding the neural mechanisms underlying social anxiety.

     

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