Tina Gupta , Helmet T. Karim , Neil P. Jones , Fabio Ferrarelli , Melissa Nance , Stephan F. Taylor , David Rogers , Ashley M. Pogue , T.H. Stanley Seah , Mary L. Phillips , Neal D. Ryan , Erika E. Forbes
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Using a randomized, counterbalanced design, we administered 3 types of TBS at different sessions: intermittent (iTBS; potentiating), continuous (cTBS; depotentiating), and sham TBS (control). We used neuronavigation to target personalized dmPFC targets based on VS-dmPFC FC. PA and negative affect (NA), and resting-state fMRI were collected pre- and post-TBS. We found no changes in PA or NA with time (pre/post), condition (iTBS, cTBS, sham), or their interaction. Functional connectivity (FC) between the nucleus accumbens and dmPFC showed a significant condition (cTBS, iTBS, and sham) by time (pre-vs. post-TBS) interaction, and post-hoc testing showed decreased pre-to post-TBS for cTBS but not iTBS or sham. For cTBS only, reduced FC pre/post stimulation was associated with increased PA (but not NA). Our findings lend support to the proposed mechanistic model of aberrant FC between the dmPFC and VS in depression and suggest a way forward for treating depression in young adults. 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引用次数: 0
摘要
抑郁症与积极情绪(PA)减弱有关,据推测这反映了前额纹状体奖赏回路的紊乱。抑郁症一直与背内侧前额叶皮层(dmPFC)激活程度较高有关,而该区域通过腹侧纹状体(VS)连接来调节 PA。抑郁症患者的低PA可能反映了dmPFC与VS功能连接(FC)的异常。为了验证这一点,我们对 29 名成年抑郁症患者(79% 为女性,年龄 = 21.4,SD = 2.04)的 dmPFC 施加了 Theta 脉冲串刺激(TBS)。我们采用随机、平衡的设计,在不同的疗程中施用了三种类型的 TBS:间歇性(iTBS;增效)、持续性(cTBS;去势)和假 TBS(对照)。我们使用神经导航技术,根据 VS-dmPFC FC 靶向个性化的 dmPFC 靶点。我们收集了TBS前后的PA和负性情绪(NA)以及静息态fMRI。我们发现 PA 或 NA 没有随时间(前/后)、条件(iTBS、cTBS、假)或它们之间的相互作用而发生变化。伏隔核和大脑前交叉韧带之间的功能连接(FC)显示出显著的条件(cTBS、iTBS和假体)与时间(TBS前与TBS后)的交互作用,事后测试显示,cTBS的TBS前与TBS后功能连接减少,而iTBS或假体则没有。仅对 cTBS 而言,刺激前/后 FC 的降低与 PA(而非 NA)的增加有关。我们的研究结果支持了所提出的抑郁症患者大脑前交叉功能区(dmPFC)和大脑后交叉功能区(VS)之间FC异常的机理模型,并为治疗青壮年抑郁症提供了一种思路。未来的研究需要评估多疗程TBS以检验临床效果。
Continuous theta burst stimulation to dorsomedial prefrontal cortex in young adults with depression: Changes in resting frontostriatal functional connectivity relevant to positive mood
Depression is associated with diminished positive affect (PA), postulated to reflect frontostriatal reward circuitry disruptions. Depression has consistently been associated with higher dorsomedial prefrontal cortex (dmPFC) activation, a region that regulates PA through ventral striatum (VS) connections. Low PA in depression may reflect dmPFC's aberrant functional connectivity (FC) with the VS. To test this, we applied theta burst stimulation (TBS) to dmPFC in 29 adults with depression (79% female, Mage = 21.4, SD = 2.04). Using a randomized, counterbalanced design, we administered 3 types of TBS at different sessions: intermittent (iTBS; potentiating), continuous (cTBS; depotentiating), and sham TBS (control). We used neuronavigation to target personalized dmPFC targets based on VS-dmPFC FC. PA and negative affect (NA), and resting-state fMRI were collected pre- and post-TBS. We found no changes in PA or NA with time (pre/post), condition (iTBS, cTBS, sham), or their interaction. Functional connectivity (FC) between the nucleus accumbens and dmPFC showed a significant condition (cTBS, iTBS, and sham) by time (pre-vs. post-TBS) interaction, and post-hoc testing showed decreased pre-to post-TBS for cTBS but not iTBS or sham. For cTBS only, reduced FC pre/post stimulation was associated with increased PA (but not NA). Our findings lend support to the proposed mechanistic model of aberrant FC between the dmPFC and VS in depression and suggest a way forward for treating depression in young adults. Future studies need to evaluate multi-session TBS to test clinical effects.
期刊介绍:
The major focus of Behaviour Research and Therapy is an experimental psychopathology approach to understanding emotional and behavioral disorders and their prevention and treatment, using cognitive, behavioral, and psychophysiological (including neural) methods and models. This includes laboratory-based experimental studies with healthy, at risk and subclinical individuals that inform clinical application as well as studies with clinically severe samples. The following types of submissions are encouraged: theoretical reviews of mechanisms that contribute to psychopathology and that offer new treatment targets; tests of novel, mechanistically focused psychological interventions, especially ones that include theory-driven or experimentally-derived predictors, moderators and mediators; and innovations in dissemination and implementation of evidence-based practices into clinical practice in psychology and associated fields, especially those that target underlying mechanisms or focus on novel approaches to treatment delivery. In addition to traditional psychological disorders, the scope of the journal includes behavioural medicine (e.g., chronic pain). The journal will not consider manuscripts dealing primarily with measurement, psychometric analyses, and personality assessment.