Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, 45219, OH, USA.
Huaxi MR Research Center (HMRRC), Department of Radiology, The Center for Medical Imaging, West China Hospital of Sichuan University, Chengdu, 610041, PR China.
Neuropsychopharmacology. 2023 Mar;48(4):615-622. doi: 10.1038/s41386-022-01463-6. Epub 2022 Oct 13.
Disruptions in the limbic system, and in emotion regulation circuitry that supports affect modulation, have been reported during acute manic episodes of bipolar disorder (BD). The impact of pharmacological treatment on these deficits, especially in youth, remains poorly characterized. 107 youths with acute manic or mixed episodes of bipolar I disorder and 60 group-matched healthy controls were recruited. Youth with bipolar disorder were randomized to double-blind treatment with quetiapine or lithium and assessed weekly. Task-based fMRI studies were performed using an identical pairs continuous performance task (CPT-IP) at pre-treatment baseline and post-treatment weeks one and six. Region of interest analyses focused on the limbic system and ventral PFC - basal ganglia - thalamocortical loop structures known to be involved in emotion regulation. Changes in regional activation were compared between the two treatment groups, and pretreatment regional activation was used to predict treatment outcome. Mania treatment scores improved more rapidly in the quetiapine than lithium treated group, as did significant normalization of neural activation toward that of healthy individuals in left amygdala (p = 0.007), right putamen (p < 0.001), and right globus pallidus (p = 0.003). Activation changes in the right putamen were correlated with reduction of mania symptoms. The limbic and emotion regulation system activation at baseline and week one predicted treatment outcome in youth with bipolar disorder with significant accuracy (up to 87.5%). Our findings document more rapid functional brain changes associated with quetiapine than lithium treatment in youth with bipolar disorder, with most notable changes in the limbic system and emotion regulation circuitry. Pretreatment alterations in these regions predicted treatment response. These findings advance understanding of regional brain alterations in youth with bipolar disorder, and show that fMRI data can predict treatment outcome before it can be determined clinically, highlighting the potential utility of fMRI biomarkers for early prediction of treatment outcomes in bipolar disorder.Clinical Trials Registration: Name: Multimodal Neuroimaging of Treatment Effects in Adolescent Mania. URL: https://clinicaltrials.gov/ . Registration number: NCT00893581.
边缘系统的紊乱,以及支持情感调节的情绪调节回路,在双相情感障碍(BD)的急性躁狂发作期间已有报道。药物治疗对这些缺陷的影响,尤其是在年轻人中,仍知之甚少。招募了 107 名患有急性躁狂或混合发作的双相 I 型障碍的年轻人和 60 名匹配的健康对照组。将双相障碍患者随机分为喹硫平或锂的双盲治疗组,并在治疗前、治疗后第 1 周和第 6 周进行每周评估。使用相同配对连续绩效任务(CPT-IP)进行基于任务的 fMRI 研究,在治疗前基线和治疗后第 1 周和第 6 周进行。重点关注已知参与情绪调节的边缘系统和腹侧前额叶皮层-基底节-丘脑皮质回路结构的感兴趣区域分析。比较了两种治疗组之间的区域激活变化,并使用治疗前区域激活来预测治疗结果。与锂治疗组相比,喹硫平治疗组的躁狂治疗评分改善更快,左杏仁核(p=0.007)、右壳核(p<0.001)和右苍白球(p=0.003)的神经激活也向健康个体正常化。右壳核的激活变化与躁狂症状的减少有关。双相障碍青年患者的基线和第 1 周的边缘系统和情绪调节系统激活可以准确预测治疗结果(高达 87.5%)。我们的研究结果记录了与锂治疗相比,喹硫平治疗与双相障碍青年患者更快的大脑功能变化,最明显的变化发生在边缘系统和情绪调节回路中。这些区域的预处理改变预测了治疗反应。这些发现增进了对双相障碍青年患者大脑区域改变的理解,并表明 fMRI 数据可以在临床上确定之前预测治疗结果,突出了 fMRI 生物标志物在双相障碍治疗结果早期预测中的潜在效用。临床试验注册:名称:青少年躁狂症的治疗效果的多模态神经影像学研究。网址:https://clinicaltrials.gov/。注册号:NCT00893581。