Reduced amygdalar gray matter volume in familial pediatric bipolar disorder

被引:186
作者
Chang, K
Karchemskiy, A
Barnea-Goraly, N
Garrett, A
Simeonova, DI
Reiss, A
机构
[1] Stanford Univ, Sch Med, Div Child & Adolescent Psychiat, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
关键词
magnetic resonance imaging; bipolar disorder; amygdala;
D O I
10.1097/01.chi.0000159948.75136.0d
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Objective: Subcortical limbic structures have been proposed to be involved in the pathophysiology of adult and pediatric bipolar disorder (BD). We sought to study morphometric characteristics of these structures in pediatric subjects with familial BD compared with healthy controls. Method: Twenty children and adolescents with BD I (mean age = 14.6 years, four females) and 20 healthy age, gender, and 10-matched controls underwent high-resolution magnetic resonance imaging at 3 T. Patients were mostly euthymic and most were taking medications. Amygdala, hippocampus, thalamus, and caudate volumes were determined by manual tracings from researchers blinded to diagnosis. Analyses of covariance were performed, with total brain volume, age, and gender as covariates. Results: No differences were found in the volumes of hippocampus, caudate, and thalamus between subjects with BD and controls. Subjects with BD had smaller volumes in the left and right amygdala, driven by reductions in gray matter volume. Exploratory analyses revealed that subjects with BD with past lithium or valproate exposure tended to have greater amygdalar gray matter volume than subjects with BD without such exposure. Conclusions: Children and adolescents with early-onset BD may have reduced amygdalar volumes, consistent with other studies in this population. Prolonged medication exposure to lithium or valproate may account for findings in adults with BD of increased amygdalar volume relative to controls.
引用
收藏
页码:565 / 573
页数:9
相关论文
共 60 条
[1]   Recognition of facial emotion in nine individuals with bilateral amygdala damage [J].
Adolphs, R ;
Tranel, D ;
Hamann, S ;
Young, AW ;
Calder, AJ ;
Phelps, EA ;
Anderson, A ;
Lee, GP ;
Damasio, AR .
NEUROPSYCHOLOGIA, 1999, 37 (10) :1111-1117
[2]   An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia [J].
Altshuler, LL ;
Bartzokis, G ;
Grieder, T ;
Curran, J ;
Jimenez, T ;
Leight, K ;
Wilkins, J ;
Gerner, R ;
Mintz, J .
BIOLOGICAL PSYCHIATRY, 2000, 48 (02) :147-162
[3]   Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia: An MRI study demonstrating neuroanatomic specificity [J].
Altshuler, LL ;
Bartzokis, G ;
Grieder, T ;
Curran, J ;
Mintz, J .
ARCHIVES OF GENERAL PSYCHIATRY, 1998, 55 (07) :663-664
[4]  
AMARAL D G, 1992, P1
[5]   The primate amygdala and the neurobiology of social behavior: Implications for understanding social anxiety [J].
Amaral, DG .
BIOLOGICAL PSYCHIATRY, 2002, 51 (01) :11-17
[6]  
ANDREASEN NC, 1977, ARCH GEN PSYCHIAT, V34, P1229
[7]  
[Anonymous], 1996, WASH U KSADS
[8]  
AYLWARD EH, 1994, AM J PSYCHIAT, V151, P687
[9]   The amygdala and reward [J].
Baxter, MG ;
Murray, EA .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (07) :563-573
[10]  
Blumberg Hilary P, 2002, Semin Clin Neuropsychiatry, V7, P243