Abstract
Objective: Anxiety is associated with increased physiological reactivity and also increased “interoceptive” sensitivity to such changes in internal bodily arousal. Joint hypermobility, an expression of a common variation in the connective tissue protein collagen, is increasingly recognized as a risk factor to anxiety and related disorders. This study explored the link between anxiety, interoceptive sensitivity and hypermobility in a sub-clinical population using neuroimaging and psychophysiological evaluation.Methods: Thirty-six healthy volunteers undertook interoceptive sensitivity tests, a clinical examination for hypermobility and completed validated questionnaire measures of state anxiety and body awareness tendency. Nineteen participants also performed an emotional processing paradigm during functional neuroimaging.Results: We confirmed a significant relationship between state anxiety score and joint hypermobility. Interoceptive sensitivity mediated the relationship between state anxiety and hypermobility. Hypermobile, compared to non-hypermobile, participants displayed heightened neural reactivity to sad and angry scenes within brain regions implicated in anxious feeling states, notably insular cortex.Conclusions: Our findings highlight the dependence of anxiety state on bodily context, and increase our understanding of the mechanisms through which vulnerability to anxiety disorders arises in people bearing a common variant of collagen.
Highlights
Anxiety is associated with heightened physiological arousal and accompanying physical sensations
We confirmed a significant relationship between state anxiety score and joint hypermobility
Interoceptive sensitivity mediated the relationship between state anxiety and hypermobility
Summary
Anxiety is associated with heightened physiological arousal and accompanying physical sensations. Interoception (i.e., sensitivity to changes in the internal physiological state of the body) is considered to be fundamental to such emotional feelings (Damasio, 1994). Responses within insula, amygdala and anterior cingulate cortex are linked both to the development and maintenance of anxiety disorders (Damsa et al, 2009; Shurick and Gross, 2013). Hyperactivity within these regions is coupled to exaggerated autonomic arousal responses (Critchley and Harrison, 2013) and occurs during anxiety symptom provocation (Holzschneider and Mulert, 2011)
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