Abstract

BackgroundCoordination of activity between the amygdala and ventromedial prefrontal cortex (vmPFC) is important for fear-extinction learning. Aberrant recruitment of this circuitry is associated with anxiety disorders. Here, we sought to determine if individual differences in future threat uncertainty sensitivity, a potential risk factor for anxiety disorders, underly compromised recruitment of fear extinction circuitry.Twenty-two healthy subjects completed a cued fear conditioning task with acquisition and extinction phases. During the task, pupil dilation, skin conductance response, and functional magnetic resonance imaging were acquired. We assessed the temporality of fear extinction learning by splitting the extinction phase into early and late extinction. Threat uncertainty sensitivity was measured using self-reported intolerance of uncertainty (IU).ResultsDuring early extinction learning, we found low IU scores to be associated with larger skin conductance responses and right amygdala activity to learned threat vs. safety cues, whereas high IU scores were associated with no skin conductance discrimination and greater activity within the right amygdala to previously learned safety cues. In late extinction learning, low IU scores were associated with successful inhibition of previously learned threat, reflected in comparable skin conductance response and right amgydala activity to learned threat vs. safety cues, whilst high IU scores were associated with continued fear expression to learned threat, indexed by larger skin conductance and amygdala activity to threat vs. safety cues. In addition, high IU scores were associated with greater vmPFC activity to threat vs. safety cues in late extinction. Similar patterns of IU and extinction learning were found for pupil dilation. The results were specific for IU and did not generalize to self-reported trait anxiety.ConclusionsOverall, the neural and psychophysiological patterns observed here suggest high IU individuals to disproportionately generalize threat during times of uncertainty, which subsequently compromises fear extinction learning. More broadly, these findings highlight the potential of intolerance of uncertainty-based mechanisms to help understand pathological fear in anxiety disorders and inform potential treatment targets.

Highlights

  • Coordination of activity between the amygdala and ventromedial prefrontal cortex is important for fear-extinction learning

  • We show that self-reported intolerance of uncertainty (IU), a personality trait implicated in the maintenance of anxiety and depressive disorders [32, 33, 31], predicts psychophysiological and neural recruitment during fear extinction learning

  • Low IU predicted reduced skin conductance response (SCR) magnitude and right amygdala activity to threat vs. safety cues, suggesting successful fear extinction, in line with previous extinction research [13, 11, 6]

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Summary

Introduction

Coordination of activity between the amygdala and ventromedial prefrontal cortex (vmPFC) is important for fear-extinction learning Aberrant recruitment of this circuitry is associated with anxiety disorders. During fear acquisition, heightened amygdala activity and increased skin conductance have been observed in response to previously neutral cues that, through conditioning, come to be associated with aversive outcomes (conditioned stimulus, CS+, e.g. shock or tone) [4, 7, 8]. Stimulation of the infralimbic cortex in rats, an area homologous to the human vmPFC, reduces responsiveness of amygdala neurons and defensive freezing behavior to conditioned tones [10] In both humans and animals, increased vmPFC activity to the CS+ has been observed in late extinction phases [6, 11], and during subsequent extinction sessions, conducted a few days after initial fear acquisition [12, 13]

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