Individual differences in striatal and amygdala response to emotional faces are related to symptom severity in social anxiety disorder.

Neuroimage Clin

Department of Psychiatry (NAC, FC, KLK, HK), University of Illinois at Chicago, 1601 W. Taylor St (M/C 912), Chicago, IL 60612, United States; Department of Psychology (FC, KLK, HK), University of Illinois at Chicago, 1007 W. Harrison St (M/C 285), Chicago, IL 60607, United States.

Published: July 2021

Social anxiety disorder (SAD) is a common heterogeneous disorder characterized by excessive fear and deficient positive experiences. Case-control emotion processing studies indicate that altered amygdala and striatum function may underlie SAD; however, links between these regions and symptomatology have yet to be established. Therefore, in the current study, 80 individuals diagnosed with SAD completed a validated emotion processing task during functional magnetic resonance imaging. Anatomy-based regions of interest were amygdala, caudate, putamen, and nucleus accumbens. Neural activity in response to angry > happy faces and fearful > happy faces in these regions were submitted to multiple linear regression analysis with bootstrapping. Additionally, multiple linear regression analysis was performed to explore clinical features of SAD. Results showed greater putamen activity and less amygdala activity in response to angry > happy faces were related to greater social anxiety severity. In the model consisting of caudate and amygdala activity in response to angry > happy faces, results were marginally related to social anxiety severity and the pattern of activity was similar to the regression model comprising putamen and amygdala. Nucleus accumbens activity was not related to social anxiety severity. There was no correspondence between brain activity in response to fearful > happy faces and social anxiety severity. Clinical variables revealed greater levels of anhedonia and general anxiety were related to social anxiety severity, however, neural activity was not related to these features of SAD. Neuroimaging findings suggest that variance in dorsal striatal and amygdala activity in response to certain social signals of threat contrasted with an approach/rewarding social signal may contribute to individual differences in SAD. Clinical findings indicate variance in anhedonia and general anxiety symptoms may contribute to individual differences in social anxiety severity.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985697PMC
http://dx.doi.org/10.1016/j.nicl.2021.102615DOI Listing

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