High dosage accelerated intermittent theta burst stimulation without precision targeting and dosing in depression: an open-label pilot study.

IF 3.7 3区 医学 Q1 CLINICAL NEUROLOGY
Miaoxi Chen, Jonas Björklund, Kai-Yen Chang, Gerrit Burkhardt, Lucia Bulubas, Simone Weller, Kristin Hagenah, Daniel Kesser, Andre R Brunoni, Frank Padberg, Ulrike Vogelmann
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Abstract

Background: High dosage accelerated intermittent theta-burst stimulation (aiTBS) protocols (10 sessions per day for 5 days) combined with precision targeting and depth adjusted iTBS intensity yield high response and remission rates in depression. However, disentangling their efficacy components to develop pragmatic mental health solutions is challenging. This pilot study applied such a high dosage aiTBS protocol without using any precision features.

Methods: Eight patients with treatment-resistant depression (TRD) underwent open-label aiTBS targeting the left dorsolateral prefrontal cortex (DLPFC) using the Beam F3 algorithm. Over 5 days, patients received 50 aiTBS sessions, each delivering 1800 pulses at 90% resting motor threshold with 50-min inter-session intervals. All patients underwent a 4 weeks follow-up without stimulation, were offered tDCS for 4 weeks thereafter and had a final follow-up after 6 months. Treatment effects were assessed by clinical and cognitive measures.

Results: Patients received 46 aiTBS sessions on average. At one-month follow-up, mean MADRS scores decreased by -12.50 ± 9.81 (Cohen's d = 2.83; 95% CI, 2.34-3.32; p < 0.001), with response and remission rates of 50% and 12.5%, respectively. After tDCS, 28.6% and 14.3% sustained response and remission, which declined to 16.7% and 0% at six months.

Conclusion: This pilot trial evidenced the antidepressant effect of a high dosage aiTBS protocol comparable with the Stanford Neuromodulation Therapy (SNT) approach but without individualized precision components. Its effectiveness appeared lower than previously reported for SNT. Randomized controlled trials should systematically investigate the contribution of precision components to the overall effectiveness of aiTBS in depression. This trial is a part of a real-world clinical study of non-invasive brain stimulation treatments conducted at our department (preregistered at DRKS-ID: DRKS00024776, drks.de).

高剂量加速间歇性θ波爆发刺激无精确靶向和剂量抑郁症:一项开放标签试点研究。
背景:高剂量加速间歇性θ -burst刺激(aiTBS)方案(每天10次,持续5天)结合精确靶向和深度调节iTBS强度可获得高疗效和缓解率。然而,理清它们的功效成分以开发实用的心理健康解决方案是具有挑战性的。该试点研究采用了如此高剂量的aiTBS方案,而没有使用任何精度特征。方法:8例难治性抑郁症(TRD)患者采用Beam F3算法对左侧背外侧前额叶皮质(DLPFC)进行开放标签aiTBS治疗。在5天的时间里,患者接受了50次aiTBS治疗,每次治疗以90%静息运动阈值提供1800次脉冲,每次治疗间隔50分钟。所有患者均接受4周无刺激随访,随后给予tDCS 4周,6个月后进行最终随访。通过临床和认知测试评估治疗效果。结果:患者平均接受46次aiTBS治疗。随访1个月,平均MADRS评分下降-12.50±9.81 (Cohen’s d = 2.83;95% ci, 2.34-3.32;结论:该试点试验证明了高剂量aiTBS方案的抗抑郁效果与斯坦福神经调节疗法(SNT)方法相当,但没有个体化精确成分。其有效性似乎低于先前报道的SNT。随机对照试验应该系统地调查精确成分对抑郁症aiTBS总体有效性的贡献。该试验是我科进行的非侵入性脑刺激治疗临床研究的一部分(DRKS-ID: DRKS00024776, drks.de)。
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来源期刊
CiteScore
8.80
自引率
4.30%
发文量
154
审稿时长
6-12 weeks
期刊介绍: The original papers published in the European Archives of Psychiatry and Clinical Neuroscience deal with all aspects of psychiatry and related clinical neuroscience. Clinical psychiatry, psychopathology, epidemiology as well as brain imaging, neuropathological, neurophysiological, neurochemical and moleculargenetic studies of psychiatric disorders are among the topics covered. Thus both the clinician and the neuroscientist are provided with a handy source of information on important scientific developments.
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