磁刺激
随机对照试验
背外侧前额叶皮质
重性抑郁障碍
功能磁共振成像
萧条(经济学)
磁共振成像
医学
心理学
物理医学与康复
前额叶皮质
神经科学
精神科
内科学
刺激
心情
放射科
认知
经济
宏观经济学
作者
Richard Morriss,Paul M. Briley,Lucy Webster,Mohamed Abdelghani,Shaun Barber,Peter Bates,Cassandra Brookes,Beth Hall,L. Ingram,Micheal Kurkar,Sudheer Lankappa,Peter F. Liddle,R. Hamish McAllister‐Williams,Alexander O’Neil-Kerr,Stefan Pszczółkowski,Ana Suazo Di Paola,Yvette Walters,Dorothee P. Auer
出处
期刊:Nature Medicine
[Springer Nature]
日期:2024-01-16
卷期号:30 (2): 403-413
被引量:39
标识
DOI:10.1038/s41591-023-02764-z
摘要
Abstract Disruption in reciprocal connectivity between the right anterior insula and the left dorsolateral prefrontal cortex is associated with depression and may be a target for neuromodulation. In a five-center, parallel, double-blind, randomized controlled trial we personalized resting-state functional magnetic resonance imaging neuronavigated connectivity-guided intermittent theta burst stimulation (cgiTBS) at a site based on effective connectivity from the right anterior insula to the left dorsolateral prefrontal cortex. We tested its efficacy in reducing the primary outcome depression symptoms measured by the GRID Hamilton Depression Rating Scale 17-item over 8, 16 and 26 weeks, compared with structural magnetic resonance imaging (MRI) neuronavigated repetitive transcranial magnetic stimulation (rTMS) delivered at the standard stimulation site (F3) in patients with ‘treatment-resistant depression’. Participants were randomly assigned to 20 sessions over 4–6 weeks of either cgiTBS ( n = 128) or rTMS ( n = 127) with resting-state functional MRI at baseline and 16 weeks. Persistent decreases in depressive symptoms were seen over 26 weeks, with no differences between arms on the primary outcome GRID Hamilton Depression Rating Scale 17-item score (intention-to-treat adjusted mean, −0.31, 95% confidence interval (CI) −1.87, 1.24, P = 0.689). Two serious adverse events were possibly related to TMS (mania and psychosis). MRI-neuronavigated cgiTBS and rTMS were equally effective in patients with treatment-resistant depression over 26 weeks (trial registration no. ISRCTN19674644).
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