Strakowski Stephen M, Fleck David E, Welge Jeffrey, Eliassen James C, Norris Matthew, Durling Michelle, Komoroski Richard A, Chu Wen-Jang, Weber Wade, Dudley Jonathan A, Blom Thomas J, Stover Amanda, Klein Christina, Strawn Jeffrey R, DelBello Melissa P, Lee Jing-Huei, Adler Caleb M
Department of Psychiatry and Behavioral Neuroscience and Center for Imaging Research, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Department of Psychiatry, Dell Medical School, University of Texas at Austin, Austin, TX, USA.
Bipolar Disord. 2016 Sep;18(6):490-501. doi: 10.1111/bdi.12426. Epub 2016 Sep 19.
We tested the hypothesis that, with treatment, functional magnetic resonance imaging (fMRI) regional brain activation in first-episode mania would normalize - i.e., that differences from healthy subjects would diminish over time, and would be associated with clinical remission status, potentially identifying neuroanatomic treatment response markers.
Forty-two participants with bipolar I disorder were recruited during their first manic episode, pseudo-randomized to open-label lithium or quetiapine, and followed for 8 weeks. fMRI scans were obtained at baseline and then after 1 and 8 weeks of treatment, while participants performed a continuous performance task with emotional distracters. Healthy participants received fMRI scans at these same intervals. Specific region-of-interest (ROI) activations within prefrontal emotional networks were assessed as potential measures of treatment response.
ROI data were reduced using exploratory factor analysis, which identified five factors that were organizationally consistent with functional anatomic models of human emotion modulation. Half of the participants with bipolar disorder achieved remission by Week 8 and were contrasted with the other half that did not. Analyses demonstrated that, in the bipolar disorder group in general, treatment led to decreases in activation across brain regions toward healthy subject values. However, differences in activation changes were observed between subjects with bipolar disorder who did or did not achieve remission in subcortical and amygdala factors.
These findings provide evidence for potential neuroanatomic treatment response markers in first-episode bipolar disorder.
我们检验了这样一个假设,即通过治疗,首次发作躁狂症患者的功能磁共振成像(fMRI)脑区激活会恢复正常——也就是说,与健康受试者的差异会随时间减少,并且会与临床缓解状态相关,这有可能识别出神经解剖学治疗反应标志物。
42名双相I型障碍患者在首次躁狂发作期间被招募,伪随机分为开放标签锂盐组或喹硫平组,并随访8周。在基线时以及治疗1周和8周后进行fMRI扫描,同时受试者执行带有情绪干扰因素的持续操作任务。健康受试者在相同时间间隔接受fMRI扫描。前额叶情绪网络内的特定感兴趣区域(ROI)激活被评估为治疗反应的潜在指标。
使用探索性因子分析减少ROI数据,该分析确定了五个在组织上与人类情绪调节功能解剖模型一致的因子。一半的双相障碍患者在第8周时实现缓解,并与未缓解的另一半患者进行对比。分析表明,总体而言,在双相障碍组中,治疗导致脑区激活朝着健康受试者的值下降。然而,在皮质下和杏仁核因子方面,实现或未实现缓解的双相障碍患者之间观察到激活变化的差异。
这些发现为首次发作双相障碍潜在的神经解剖学治疗反应标志物提供了证据。