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Relationship between anxiety, perceived pain and pain-related brain activation
Morten S. Hadsel, DDS1, Yoshitetsu Oshiro, MD, PhD1, Alexandre Quevedo, DDS1, Robert A. Kraft, PhD2, and Robert C. Coghill, PhD1. (1) Department of Neurobiology and Anatomy, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1010, (2) Division of Radiological Sciences, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1010
Emotions and factors like cognition and attention shape the pain experience in a context-dependent way. Our aim was to assess the relationship between anxiety and perceived pain-intensity, and to investigate the contribution of anxiety to stimulus and peri-stimulus changes in brain activation induced by experimental heat pain. Employing a block design, we acquired fMRI data from 12 healthy volunteers that were given cutaneous painful heat stimuli. Stimulus-related pain intensity was rated retrospectively on a 0-10 VAS scale. The Anxiety Scale raw scores of the Brief Symptom Inventory® (Pearson Assessments) were introduced as a co-variate of interest in the fMRI analysis (FSL, Oxford Centre for fMRI of the Brain, Software Library). Psychophysical/-metric analyses revealed that anxiety was negatively correlated with perceived pain intensity (r = -0.69, p = 0.01). FMRI analyses indicated that the stimulus- and the pre- and post-stimulus periods exhibited typical pain-related activation/deactivation patterns. Anxiety-related activation was only detected in the left (contralateral) middle temporal gyrus (MTG) (Brodmann's area 21)/temporoparietal junction (TPJ) and was only present during painful stimulation and not during the peri-stimulus periods. No anxiety-related deactivations could be identified. Apart from its main functions in auditory/language and associative processing, the anxiety-activated right temporal area has been implicated in mood disorders and as a detector of changes in the sensory environment. Our preliminary results suggest a role of MTG/TPJ in an up-regulated awareness of dynamic sensory changes in anxious subjects, resulting in activation of antinociceptive systems.
