萧条(经济学)
功能磁共振成像
医学
神经导航
扣带回前部
重性抑郁障碍
磁刺激
背外侧前额叶皮质
病人健康调查表
最小意识状态
刺激
静息状态功能磁共振成像
磁共振成像
听力学
物理医学与康复
心理学
物理疗法
前额叶皮质
精神科
抑郁症状
内科学
神经科学
心情
放射科
认知
意识
宏观经济学
经济
作者
Erica Nakano,Peter Sedaros,Vivian Hoang,Joyce Pi,Julie Di Marco,S. Shankar,Gloria Pai,Vincenzo De Luna,Shan Siddiqi,Nathan Meng,Danielle D. DeSouza,David Carreon
标识
DOI:10.1016/j.brs.2023.07.032
摘要
Background: Accelerated intermittent theta-burst stimulation (aiTBS) using resting-state functional magnetic resonance imaging (fMRI)-based neuronavigation was recently cleared by the FDA for use in adults with depression. The objective of this study was to gauge the clinical utility of fMRI-guided neuronavigation in adolescents with depression. Methods: Three individuals (male, 16-17 years) underwent resting-state fMRI scanning prior to treatment. Individualized left dorsolateral prefrontal cortex (DLPFC) brain targets were derived for each patient based on resting-state functional connectivity to the subgenual anterior cingulate cortex. aiTBS treatments were administered via the MagVenture MagPro R30 system and a MagVenture Cool-B65 coil, paired with the Localite TMS Navigator. Patients received 50 stimulation sessions over five days (8 to 11 sessions per day, spaced by a minimum of 50 minutes). Self-reported depression symptoms were evaluated pre- and one-week post-treatment using the Patient Health Questionnaire-9 (PHQ-9). Results: Baseline PHQ-9 scores were 20, 19, and 19 for each patient indicating moderately-severe to severe symptoms. Following treatment, scores decreased to 3, 2 and 12, respectively indicating two patients achieved remission and no longer had depressive symptoms (85% and 89% reduction in symptom severity). One patient was considered a non-responder, however still achieved a 37% reduction in symptom severity. Conclusions: fMRI-guided aiTBS treatment was well tolerated by all three patients. This case series provides evidence that neuronavigated aiTBS may be a safe and effective treatment for some adolescents with depression. Future studies should examine the safety, efficacy, and durability in a larger randomized sham-controlled trial. Conflicts of Interest: None Funding: None Disclosures: None
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