Self-Other Neural Representational Distinction is Associated with Distorted Social Predictions in Social Anxiety
Yanyan QiiD, Yun Chen, Yixiao Hu, Qianqian Fan, Lingxiao WangiD, Guochun YangiD, Grit Hein, Haiyan WuiD
Abstract
Background: Social anxiety (SA) is characterized by distorted negative expectations about the future. Because optimism bias is inherently comparative, the extent to which these predictions reflect a fundamental disruption in self- versus other-referential processing remains poorly understood. Methods: Across two experiments, we investigated the mechanisms underlying social predictions in SA. In Experiment 1, individuals with high (n = 52, LSAS > 65) and low SA (n = 51, LSAS < 35) rated the future likelihood of positive and negative social outcomes for themselves or for a protagonist. In Experiment 2, 35 adults spanning a continuous spectrum of SA completed the task during fMRI. Behavior was analyzed using linear mixed-effects models. Neurally, multivariate pattern analysis (MVPA) quantified self-other representational distinctions, while a parametric general linear model (GLM) tracked neural sensitivity to likelihood predictions. Results: Behaviorally, higher SA was characterized by an attenuated optimism bias: individuals predicted a lower likelihood of positive outcomes, but a higher likelihood of negative outcomes, for themselves compared to others. Neurally, higher trait SA correlated with greater self-other representational distinction within the left pregenual anterior cingulate cortex (pgACC). Concurrently, the precuneus exhibited stronger parametric tracking of self-negative predictions versus others. Crucially, pgACC representational distinction during positive outcome processing significantly mediated the association between SA severity and heightened prediction-tracking in the precuneus. Conclusions: These findings offer a novel mechanistic framework, suggesting that an exaggerated neural segregation of the self from others drives hyper-vigilant, risk-sensitive social predictions in SA. This candidate circuit-level dynamic warrants further replication in clinical cohorts.
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