Neurophysiological effects of multiple mood episodes in bipolar disorder

被引:21
作者
Borgelt, Logan [1 ]
Strakowski, Stephen M. [1 ,2 ]
DelBello, Melissa P. [1 ]
Weber, Wade [1 ]
Eliassen, James C. [1 ]
Komoroski, Richard A. [1 ]
Chu, Wen-Jang [1 ,3 ]
Welge, Jeffrey A. [1 ]
Blom, Thomas J. [1 ]
Rummelhoff, Emily [1 ]
Tallman, Maxwell [1 ]
Lee, Jing-Huei [3 ]
Adler, Caleb M. [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH USA
[2] Univ Texas Austin, Dept Psychiat, Dell Med Sch, Austin, TX 78712 USA
[3] Univ Cincinnati, Coll Engn & Appl Sci, Dept Biomed Engn, Cincinnati, OH USA
关键词
bipolar disorder; fMRI; mania; MRS; neuroprogression; MAGNETIC-RESONANCE-SPECTROSCOPY; FMRI; ACTIVATION; ILLNESS; MEMORY; METAANALYSIS; ATTENTION; COGNITION; AMYGDALA; SYSTEMS;
D O I
10.1111/bdi.12782
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives Bipolar disorder is marked by progressive symptomatic changes, which have been linked with episode-related structural findings-particularly in the prefrontal cortex. However, few studies have examined neurofunctional and neurochemical effects of disease burden. In this study, we compared first- and multi-episode bipolar individuals. We hypothesized that the latter would demonstrate evidence of neurophysiological differences consistent with a model of progressive functional degradation of these networks. Methods First- and multi-episode manic bipolar subjects participated in functional magnetic resonance imaging (fMRI) including a continuous performance task with emotional distractors, and in single-voxel (H-1) magnetic resonance spectroscopy (MRS). A priori fMRI regions-of-interest (ROI) included structures comprising prefrontal-striatal-amygdala networks; (H-1)MRS voxels were placed within bilateral ventrolateral prefrontal (VLPFC) and anterior cingulate cortex (ACC). Both ROI and voxel-based brain activation in response to emotional stimuli, and neurochemical concentrations derived from (H-1)MRS were compared across bipolar groups. Results Multi-episode bipolar subjects showed relatively lower regional activation across prefrontal-striatal-amygdala networks, including bilateral VLPFC, orbitofrontal cortex, ACC, putamen, caudate, and amygdala. Exploratory whole-brain, voxel-based analysis suggested additional areas of lower activation extending into Brodmann area 22, posterior parietal regions, and right thalamus. Glutamate and N-acetylaspartate (NAA) concentrations were also relatively lower in the ACC of multi-episode subjects. Conclusions Disease burden, exemplified by multiple affective episodes is associated with evidence of widespread decrements in affective network activity. Lower ACC NAA concentration is similarly consistent with a model of progressive functional deficits. These findings support the functional significance of previously observed progressive structural changes throughout these regions.
引用
收藏
页码:503 / 513
页数:11
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