Individual differences in social behavior predict amygdala response to fearful facial expressions in Williams syndrome

被引:47
作者
Haas, Brian W. [1 ]
Hoeft, Fumiko [1 ]
Searcy, Yvonne M. [2 ]
Mills, Debra [3 ]
Bellugi, Ursula [2 ]
Reiss, Allan [1 ]
机构
[1] Stanford Univ, Sch Med, CIBSR, Stanford, CA 94305 USA
[2] Salk Inst Biol Studies, Cognit Neurosci Lab, San Diego, CA 92138 USA
[3] Bangor Univ, Sch Psychol, Bangor, Gwynedd, Wales
关键词
Williams syndrome; Emotion; Social neuroscience; Amygdala; Social fearlessness; functional Magnetic Resonance Imaging; GENETIC INFLUENCES; YOUNG-CHILDREN; D PERSONALITY; HYPERSOCIABILITY; COGNITION; BRAIN; APPROACHABILITY; SOCIABILITY; PERCEPTION; EVERYBODY;
D O I
10.1016/j.neuropsychologia.2009.12.030
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Williams syndrome (WS) is a genetic condition often paired with abnormal social functioning and behavior. In particular, those with WS are characterized as being relatively hypersocial, overly emotional/empathic, and socially uninhibited or fearless. In addition, WS is associated with abnormal amygdala structure and function. Very little is known however about the relationship between specific social behaviors and altered amygdala function in WS. This study was designed to compare three models that relate abnormal social behavior with amygdala function in WS (indiscriminate sociability, emotional and empathic sociability and social fearlessness). We used a social behavior assessment procedure (Salk Institute Sociability Questionnaire), functional magnetic resonance imaging and an implicit emotion face processing task to test these models. Our findings provide support for a model of abnormal social fearlessness by showing that in WS, abnormal amygdala response to fear is paired with an increased tendency to approach strangers. Specifically, individuals with WS that exhibited less amygdala response to fearful facial expressions (compared to neutral) also exhibited an increased tendency to approach strangers. These findings contribute to our understanding of social and emotional functioning in neurodevelopmental conditions and provide evidence that in WS, amygdala response to fear modulates social behavior. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1283 / 1288
页数:6
相关论文
共 43 条
[1]   The human amygdala in social judgment [J].
Adolphs, R ;
Tranel, D ;
Damasio, AR .
NATURE, 1998, 393 (6684) :470-474
[2]   Towards the neural basis for hypersociability in a genetic syndrome [J].
Bellugi, U ;
Adolphs, R ;
Cassady, C ;
Chiles, M .
NEUROREPORT, 1999, 10 (08) :1653-1657
[3]   Affect, social behavior, and the brain in Williams syndrome [J].
Bellugi, Ursula ;
Jarvinen-Pasley, Anna ;
Doyle, Teresa F. ;
Reilly, Judy ;
Reiss, Allan L. ;
Korenberg, Julie R. .
CURRENT DIRECTIONS IN PSYCHOLOGICAL SCIENCE, 2007, 16 (02) :99-104
[4]   Friendly faces and unusual minds [J].
Bhattacharjee, Y .
SCIENCE, 2005, 310 (5749) :802-804
[5]   Amygdala response to happy faces as a function of extraversion [J].
Canli, T ;
Sivers, H ;
Whitfield, SL ;
Gotlib, IH ;
Gabrieli, JDE .
SCIENCE, 2002, 296 (5576) :2191-2191
[6]  
Costa P.T., 1992, Revised NE0 personality inventory and NE0 five-factor inventory professional manual
[7]   Adults with Williams syndrome - Preliminary study of social, emotional and behavioural difficulties [J].
Davies, M ;
Udwin, O ;
Howlin, P .
BRITISH JOURNAL OF PSYCHIATRY, 1998, 172 :273-276
[8]   Decreased differential activity in the amygdala in response to fearful expressions in Type D personality [J].
de Geder, B. ;
van de Riet, W. A. C. ;
Grezes, J. ;
Denollet, J. .
NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY, 2008, 38 (03) :163-169
[9]   DS14: Standard assessment of negative affectivity, social inhibition, and Type D personality [J].
Denollet, J .
PSYCHOSOMATIC MEDICINE, 2005, 67 (01) :89-97
[10]   Williams syndrome: A genetic deletion disorder presenting clues to the biology of sociability and clinical challenges of hypersociability [J].
Deutsch, Stephen I. ;
Rosse, Richard B. ;
Schwartz, Barbara L. .
CNS SPECTRUMS, 2007, 12 (12) :903-907