Amygdala response to faces parallels social behavior in Williams syndrome

被引:21
作者
Paul, Brianna M. [1 ]
Snyder, Abraham Z. [2 ,3 ]
Haist, Frank [4 ]
Raichle, Marcus E. [2 ,3 ,5 ,6 ]
Bellugi, Ursula [7 ]
Stiles, Joan [8 ]
机构
[1] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90095 USA
[2] Washington Univ, Dept Radiol, St Louis, MO USA
[3] Washington Univ, Dept Neurol, St Louis, MO USA
[4] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[5] Washington Univ, Dept Biomed Engn, St Louis, MO USA
[6] Washington Univ, Dept Anat & Neurobiol, St Louis, MO USA
[7] Salk Inst Biol Studies, Cognit Neurosci Lab, La Jolla, CA 92037 USA
[8] Univ Calif San Diego, Dept Cognit Sci, La Jolla, CA 92093 USA
关键词
Williams syndrome; face processing; amygdala; fMRI; social cognition; BRAIN ACTIVATION; NEURAL BASIS; ADULTS; COGNITION; FMRI; HYPERSOCIABILITY; NORMALIZATION; NEUROBIOLOGY; CHILDREN; SYSTEMS;
D O I
10.1093/scan/nsp023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Individuals with Williams syndrome (WS), a genetically determined disorder, show relatively strong face-processing abilities despite poor visuospatial skills and depressed intellectual function. Interestingly, beginning early in childhood they also show an unusually high level of interest in face-to-face social interaction. We employed functional magnetic resonance imaging (fMRI) to investigate physiological responses in face-sensitive brain regions, including ventral occipito-temporal cortex and the amygdala, in this unique genetic disorder. Participants included 17 individuals with WS, 17 age- and gender-matched healthy adults (chronological age-matched controls, CA) and 17 typically developing 8- to 9-year-old children (developmental age controls, DA). While engaged in a face discrimination task, WS participants failed to recruit the amygdala, unlike both CA and DA controls. WS fMRI responses in ventral occipito-temporal cortex, however, were comparable to those of DA controls. Given the integral role of the amygdala in social behavior, the failure of WS participants to recruit this region during face processing may be a neural correlate of the abnormally high sociability that characterizes this disorder.
引用
收藏
页码:278 / 285
页数:8
相关论文
共 58 条
[1]   The human amygdala in social judgment [J].
Adolphs, R ;
Tranel, D ;
Damasio, AR .
NATURE, 1998, 393 (6684) :470-474
[2]   Role of the amygdala in processing visual social stimuli [J].
Adolphs, Ralph ;
Spezio, Michael .
UNDERSTANDING EMOTIONS, 2006, 156 :363-378
[3]   The primate amygdala and the neurobiology of social behavior: Implications for understanding social anxiety [J].
Amaral, DG .
BIOLOGICAL PSYCHIATRY, 2002, 51 (01) :11-17
[4]   AMYGDALO-CORTICAL PROJECTIONS IN THE MONKEY (MACACA-FASCICULARIS) [J].
AMARAL, DG ;
PRICE, JL .
JOURNAL OF COMPARATIVE NEUROLOGY, 1984, 230 (04) :465-496
[5]   Brain activation during face perception: Evidence of a developmental change [J].
Aylward, EH ;
Park, JE ;
Field, KM ;
Parsons, AC ;
Richards, TL ;
Cramer, SC ;
Meltzoff, AN .
JOURNAL OF COGNITIVE NEUROSCIENCE, 2005, 17 (02) :308-319
[6]  
BEERY KE, 1997, BEERYBUKTENICA DEV T
[7]   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
[8]   Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome [J].
Bellugi, U ;
Lichtenberger, L ;
Mills, D ;
Galaburda, A ;
Korenberg, JR .
TRENDS IN NEUROSCIENCES, 1999, 22 (05) :197-207
[9]  
Bellugi U., 1994, Atypical cognitive deficits in developmental disorders: Implications for brain function, P23
[10]  
Bellugi U., 2001, Journey from cognition to brain to gene: Perspectives from Williams syndrome