O'Reardon John P, Solvason H Brent, Janicak Philip G, Sampson Shirlene, Isenberg Keith E, Nahas Ziad, McDonald William M, Avery David, Fitzgerald Paul B, Loo Colleen, Demitrack Mark A, George Mark S, Sackeim Harold A
Department of Psychiatry, University of Pennsylvania, 3535 Market Street, Philadelphia, PA 19014, USA.
Biol Psychiatry. 2007 Dec 1;62(11):1208-16. doi: 10.1016/j.biopsych.2007.01.018. Epub 2007 Jun 14.
We tested whether transcranial magnetic stimulation (TMS) over the left dorsolateral prefrontal cortex (DLPFC) is effective and safe in the acute treatment of major depression.
In a double-blind, multisite study, 301 medication-free patients with major depression who had not benefited from prior treatment were randomized to active (n = 155) or sham TMS (n = 146) conditions. Sessions were conducted five times per week with TMS at 10 pulses/sec, 120% of motor threshold, 3000 pulses/session, for 4-6 weeks. Primary outcome was the symptom score change as assessed at week 4 with the Montgomery-Asberg Depression Rating Scale (MADRS). Secondary outcomes included changes on the 17- and 24-item Hamilton Depression Rating Scale (HAMD) and response and remission rates with the MADRS and HAMD.
Active TMS was significantly superior to sham TMS on the MADRS at week 4 (with a post hoc correction for inequality in symptom severity between groups at baseline), as well as on the HAMD17 and HAMD24 scales at weeks 4 and 6. Response rates were significantly higher with active TMS on all three scales at weeks 4 and 6. Remission rates were approximately twofold higher with active TMS at week 6 and significant on the MADRS and HAMD24 scales (but not the HAMD17 scale). Active TMS was well tolerated with a low dropout rate for adverse events (4.5%) that were generally mild and limited to transient scalp discomfort or pain.
Transcranial magnetic stimulation was effective in treating major depression with minimal side effects reported. It offers clinicians a novel alternative for the treatment of this disorder.
我们测试了经颅磁刺激(TMS)作用于左侧背外侧前额叶皮质(DLPFC)在重度抑郁症急性治疗中是否有效且安全。
在一项双盲、多中心研究中,301例未服用药物且之前治疗无效的重度抑郁症患者被随机分为接受活性TMS组(n = 155)或假TMS组(n = 146)。每周进行5次治疗,TMS频率为每秒10次脉冲,强度为运动阈值的120%,每次治疗3000次脉冲,持续4 - 6周。主要结局是在第4周时用蒙哥马利 - 阿斯伯格抑郁评定量表(MADRS)评估的症状评分变化。次要结局包括17项和24项汉密尔顿抑郁评定量表(HAMD)的变化以及用MADRS和HAMD评估的缓解率和反应率。
在第4周时,活性TMS在MADRS上显著优于假TMS(对基线时两组症状严重程度不平等进行事后校正),在第4周和第6周时在HAMD17和HAMD24量表上也是如此。在第4周和第6周时,活性TMS在所有三个量表上的反应率均显著更高。在第6周时,活性TMS的缓解率约高出两倍,在MADRS和HAMD24量表上具有显著性(但在HAMD17量表上不显著)。活性TMS耐受性良好,不良事件脱落率低(4.5%),不良事件一般较轻,仅限于短暂的头皮不适或疼痛。
经颅磁刺激在治疗重度抑郁症方面有效,且报告的副作用最小。它为临床医生提供了一种治疗该疾病的新选择。