Park Sunyoung, Choi Won-Jung, Kim Sejoo, Kim Borah, Son Sang Joon, Roh Daeyoung, Kim Woo Jung, Park Jin Young
Department of Psychiatry, National Health Insurance Corporation Ilsan Hospital, Goyang, Republic of Korea.
Gangnam Yonsei Psychiatry Clinic, Seoul, South Korea; Department of Psychiatry, Yonsei University College of Medicine, Seoul, Republic of Korea.
J Psychiatr Res. 2020 Aug;127:42-47. doi: 10.1016/j.jpsychires.2020.04.012. Epub 2020 May 8.
We compared the efficacy and safety of transcranial direct current stimulation (tDCS) vs. Sertraline in the treatment of Major Depressive Disorder (MDD) in South Korean participants. This was a multi-center, double blind, active controlled study with non-inferiority testing. Patients were randomly assigned to receive tDCS (n = 45) or Sertraline (n = 47). tDCS was administered in 30-min, 2 mA prefrontal stimulation sessions for 10 consecutive weekdays, followed by 2 treatments at 4 and 6 weeks. Sertraline was administered at a dose of 50 mg per day for 6 weeks. The primary outcome measure was a change in the Montgomery-Asberg Depression Rating Scale (MADRS) score at six weeks. Mean MADRS scores decreased by 14.58 ± 8.51 points in the tDCS group and 12.32 ± 8.56 points in the Sertraline group. There was no significant main effect of group (p = 0.5877) or time by group interaction across weeks 0, 3, and 6 (p = 0.1539). Noninferiority of tDCS compared with Sertraline was not demonstrated. The mean difference between the Sertraline and tDCS group was -2.258 (95% confidence interval [CI], -5.795 to 1.27811), and the lower boundary of the CI was lower than the prespecified noninferiority margin of -3.56. There were no significant group differences in the rate of adverse events. In the present study, the noninferiority of tDCS to Sertraline for the treatment of depression was not found in this Korean population.
我们比较了经颅直流电刺激(tDCS)与舍曲林在韩国参与者中治疗重度抑郁症(MDD)的疗效和安全性。这是一项多中心、双盲、活性对照的非劣效性试验研究。患者被随机分配接受tDCS(n = 45)或舍曲林(n = 47)治疗。tDCS采用2毫安的前额叶刺激,每次30分钟,连续10个工作日进行,随后在第4周和第6周各进行2次治疗。舍曲林以每日50毫克的剂量服用6周。主要结局指标是6周时蒙哥马利-阿斯伯格抑郁量表(MADRS)评分的变化。tDCS组的MADRS平均得分下降了14.58±8.51分,舍曲林组下降了12.32±8.56分。在第0、3和6周,组间没有显著的主效应(p = 0.5877),组与时间之间也没有显著的交互作用(p = 0.1539)。未证明tDCS相对于舍曲林的非劣效性。舍曲林组和tDCS组之间的平均差异为-2.258(95%置信区间[CI],-5.795至1.27811),CI的下限低于预先设定的非劣效性边界-3.56。不良事件发生率在两组之间没有显著差异。在本研究中,未发现tDCS在治疗抑郁症方面相对于舍曲林在韩国人群中的非劣效性。