Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Journal Article (Journal Article)

Williams syndrome (WS) is a rare genetic disorder caused by the deletion of approximately 25 genes on chromosome 7q11.23 and is characterized by both hypersociability and increases in specific phobia and anticipatory anxiety regarding non-social entities or circumstances. Alterations in amygdala reactivity and prefrontal regulation consistent with the observed behavioral pattern of social versus non-social abnormalities have been previously demonstrated in individuals with WS (Meyer-Lindenberg et al., 2005). However, in that study, the social stimulus (faces) matching task was more difficult than the non-social scene (IAPS stimuli) matching task, making it impossible to disambiguate the relative contributions of task difficulty and stimulus type (social versus non-social). In the present study, we examined the performance of the same group of participants with WS and normal IQs during a more cognitively demanding task using the same scene stimuli as in the prior study. Confirming previous findings, the results indicated (a) a differential response of prefrontal regions as a function of task difficulty and (b) a persistently increased activation of the amygdala to non-social scenes by individuals with WS regardless of cognitive load. These data provide further evidence of disruption in amygdala-prefrontal circuitry in individuals with WS.

Full Text

Duke Authors

Cited Authors

  • Muñoz, KE; Meyer-Lindenberg, A; Hariri, AR; Mervis, CB; Mattay, VS; Morris, CA; Berman, KF

Published Date

  • March 2010

Published In

Volume / Issue

  • 50 / 1

Start / End Page

  • 340 - 346

PubMed ID

  • 20004252

Pubmed Central ID

  • PMC3013360

Electronic International Standard Serial Number (EISSN)

  • 1095-9572

International Standard Serial Number (ISSN)

  • 1053-8119

Digital Object Identifier (DOI)

  • 10.1016/j.neuroimage.2009.11.069


  • eng