Non-invasive electrical and magnetic stimulation of the brain, spinal cord and roots: basic principles and procedures for routine clinical application. Report of an IFCN committee

磁刺激 哈姆德 耐受性 医学 精神运动学习 重性抑郁障碍 神经科学 刺激 随机对照试验 不利影响 物理医学与康复 听力学 精神科 心理学 内科学 认知 焦虑
作者
Paolo Maria Rossini,A.T. Barker,Alfredo Berardelli,M.D. Caramia,Giuseppe Caruso,Roger Q. Cracco,M.R. Dimitrijević,Mark Hallett,Yoshiaki Katayama,C.H. Lücking,A.L. Maertens de Noordhout,C. D. Marsden,N.M.F. Murray,John C. Rothwell,Michael Swash,Claude Tomberg
出处
期刊:Electroencephalography and Clinical Neurophysiology [Elsevier]
卷期号:91 (2): 79-92 被引量:2961
标识
DOI:10.1016/0013-4694(94)90029-9
摘要

Repetitive transcranial magnetic stimulation (rTMS) at left dorsolateral prefrontal cortex (lDLPFC) is commonly used in major depressive disorder (MDD), even though its therapeutic efficacy is limited. Given that many MDD patients show psychomotor retardation, we aim to examine whether the left motor cortex (lMC) as a novel rTMS target would provide effective and well-tolerated treatment as being comparable to lDLPFC-rTMS.In this prospective double-blind randomized single-center study, 131 MDD patients were randomly assigned to the lDLPFC or lMC group and were treated with 10 Hz rTMS (90 % motor threshold) applied twice daily for 4000 pulses continuously over five days. The primary endpoint was the Hamilton Depression Scale (HAMD) total score change after treatment.After the five-day rTMS treatment, there was no significant difference in both HAMD reduction rate (lDLPFC 59.3 % ± 20.4 %, lMC 51.3 % ± 26.3 %, P = 0.10) and adverse effects (P = 0.79) between 48 (73.8 %) lMC subjects and 51 (77.3 %) lDLPFC subjects. Furthermore, the lMC study group showed stable HAMD scores at follow-up compared to their endpoint scores (P = 0.08).Sham-control group was not included and the sample size was small. Therefore, our results should be seen as exploratory and preliminary.The preliminary good therapeutic response, comparability, and tolerability of lMC-rTMS suggest lMC a potential and more easily accessible rTMS target. Together, our findings raise the possibility of symptom-specific rTMS in motor cortex (psychomotor retardation) or lDLPFC (cognitive deficits). This warrants larger clinical trials of rTMS in MDD with symptom-specific stimulation targets.
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