The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings

被引:608
作者
Strakowski, SM
DelBello, MP
Adler, CM
机构
[1] Univ Cincinnati, Coll Med, Ctr Imaging Res, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Coll Med, Bipolar & Psychot Disorders Res Program, Cincinnati, OH USA
关键词
MRI; MRS; fMRI; neuroimaging; neurophysiology;
D O I
10.1038/sj.mp.4001585
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The authors review existing structural and functional neuroimaging studies of patients with bipolar disorder and discuss how these investigations enhance our understanding of the neurophysiology of this illness. Findings from structural magnetic resonance imaging (MRI) studies suggest that some abnormalities, such as those in prefrontal cortical areas (SGPFC), striatum and amygdala exist early in the course of illness and, therefore, potentially, predate illness onset. In contrast, other abnormalities, such as those found in the cerebellar vermis, lateral ventricles and other prefrontal regions (eg, left inferior), appear to develop with repeated affective episodes, and may represent the effects of illness progression and associated factors. Magnetic resonance spectroscopy investigations have revealed abnormalities of membrane and second messenger metabolism, as well as bioenergetics, in striatum and prefrontal cortex. Functional imaging studies report activation differences between bipolar and healthy controls in these same anterior limibic regions. Together, these studies support a model of bipolar disorder that involves dysfunction within subcortical ( striatal thalamic)-prefrontal networks and the associated limbic modulating regions ( amygdala, midline cerebellum). These studies suggest that, in bipolar disorder, there may be diminished prefrontal modulation of subcortical and medial temporal structures within the anterior limbic network ( eg, amygdala, anterior striatum and thalamus) that results in dysregulation of mood. Future prospective and longitudinal studies focusing on these specific relationships are necessary to clarify the functional neuroanatomy of bipolar disorder.
引用
收藏
页码:105 / 116
页数:12
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