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Shruti Kinger

Publications and source records attributed to Shruti Kinger.

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Intrinsic Brain Networks Underlying the Experience and Expression of Subclinical Anxiety

Anxiety includes behavioural, physiological, and subjective components that do not always align, and it remains unclear whether these dimensions are supported by distinct intrinsic brain networks. Guided by the two-system framework, we tested whether resting-state functional connectivity (rsFC) differentiates these components in subclinical anxiety. Forty-seven young adults spanning a range of subclinical anxiety levels completed a threat anticipation task measuring behavioral responses (reaction time) and physiological arousal (skin conductance), along with the NIH Fear-Affect self-report of anxiety severity. These measures were related to rsFC using region-of-interest analyses. Higher subclinical anxiety was associated with faster responses under temporally uncertain threat, consistent with increased vigilance, while no association was found with physiological arousal. At the neural level, three connectivity patterns emerged and remained significant after sequential family-wise error correction. Behavioural responses modulated by subclinical anxiety were linked to stronger connectivity between the anterior cingulate cortex (ACC) and insula. Physiological modulation was associated with connectivity between the ACC and orbitofrontal cortex (OFC). Subjective anxiety was associated with increased connectivity between the hippocampus and insula. Additional connections were observed but did not survive stricter correction. Overall, the findings indicate that behavioural, physiological, and subjective aspects of subclinical anxiety map onto partially dissociable but overlapping intrinsic brain networks, extending prior task-based results to resting-state connectivity and informing future work on early neural markers of anxiety.

q-bio.NC

Resting-State Functional Connectivity Correlates of Emotional Memory Control under Cognitive load in Subclinical Anxiety

Volitional memory control supports adaptive cognition by enabling intentional suppression of goal-irrelevant, interfering memories and recall of goal-relevant memories. Neural mechanisms of suppression and recall have been studied largely in isolation, and their operation under concurrent working memory load in the context of subclinical anxiety remains unclear. We examined control of emotionally valenced memories in 47 healthy participants with varying levels of subclinical anxiety under dual-task conditions involving directed suppression and recall while concurrently performing a secondary task imposing visual working memory load. Cognitive efficiency in controlling dual-task memory-linked interference, measured by the Balanced Integration Score (BIS), showed no differences between suppression and recall, across emotions, or by anxiety. Intrinsic functional brain networks measured by seed-to-voxel resting-state functional connectivity (rsFC) revealed dissociable rsFC profiles linked to cognitive control across emotional valences, moderated by anxiety. Efficient suppression of positive memories correlated with reduced connectivity between anterior cingulate cortex and posterior perceptual-midline regions, and diminished hippocampal-frontal pole coupling. Efficient suppression of negative memories correlated with increased posterior parietal to lateral occipital connectivity. Anxiety moderated associations between cognitive control and prefrontal connectivity during suppression of positive memories and recall of positive and neutral memories. Direct comparisons revealed stronger hippocampal-thalamic rsFC during suppression versus recall of positive memories. Together, these findings delineate neural correlates of volitional emotional memory control under cognitive load and suggest that subclinical anxiety shapes these networks selectively

q-bio.NC