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Changes in the brain structural connectome after a prospective randomized clinical trial of lithium and quetiapine treatment in youth with bipolar disorder.在一项针对双相情感障碍青少年的锂盐和喹硫平治疗前瞻性随机临床试验后,大脑结构连接组的变化。
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Neurophysiological effects of multiple mood episodes in bipolar disorder.双相情感障碍中多次情绪发作的神经生理学影响。
Bipolar Disord. 2019 Sep;21(6):503-513. doi: 10.1111/bdi.12782. Epub 2019 Jun 10.
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A BRIEF INTRODUCTION TO THE NEUROGENETICS OF COGNITION-EMOTION INTERACTIONS.认知-情绪相互作用的神经遗传学简介
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An evaluation of the efficacy, reliability, and sensitivity of motion correction strategies for resting-state functional MRI.评价静息态功能磁共振成像中运动校正策略的疗效、可靠性和敏感性。
Neuroimage. 2018 May 1;171:415-436. doi: 10.1016/j.neuroimage.2017.12.073. Epub 2017 Dec 24.
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Prediction of lithium response in first-episode mania using the LITHium Intelligent Agent (LITHIA): Pilot data and proof-of-concept.使用锂智能代理(LITHIA)预测首发躁狂症的锂反应:试点数据与概念验证
Bipolar Disord. 2017 Jun;19(4):259-272. doi: 10.1111/bdi.12507. Epub 2017 Jun 2.
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fMRI brain activation changes following treatment of a first bipolar manic episode.首次双相躁狂发作治疗后的功能磁共振成像脑激活变化
Bipolar Disord. 2016 Sep;18(6):490-501. doi: 10.1111/bdi.12426. Epub 2016 Sep 19.
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The Human Brainnetome Atlas: A New Brain Atlas Based on Connectional Architecture.人类脑网络组图谱:基于连接结构的新脑图谱。
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Pharmacotherapy of bipolar disorder with quetiapine: a recent literature review and an update.喹硫平治疗双相情感障碍:近期文献综述与更新
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Neurofunctional effects of quetiapine in patients with bipolar mania.喹硫平对双相躁狂症患者的神经功能影响。
Bipolar Disord. 2015 Jun;17(4):444-9. doi: 10.1111/bdi.12274. Epub 2014 Oct 31.
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The effects of carbamazepine on prefrontal activation in manic youth with bipolar disorder.卡马西平对双相情感障碍躁狂期青少年前额叶激活的影响。
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双相障碍青少年急性躁狂或混合发作期短期喹硫平与锂治疗对边缘系统及情绪调节回路的影响。

Effects of short-term quetiapine and lithium therapy for acute manic or mixed episodes on the limbic system and emotion regulation circuitry in youth with bipolar disorder.

机构信息

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.

出版信息

Neuropsychopharmacology. 2023 Mar;48(4):615-622. doi: 10.1038/s41386-022-01463-6. Epub 2022 Oct 13.

DOI:10.1038/s41386-022-01463-6
PMID:36229596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9938175/
Abstract

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.

摘要

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。