Nguyen Quoc Khoa David, Solanki Pravik, Thomas Elizabeth H X, Cerins Andris, Hahn Lisa, Galletly Cherrie, Fitzgerald Paul B, Chen Leo
Alfred Mental and Addiction Health, Alfred Health, Level 4, 607 St Kilda Road, Melbourne, Victoria 3004, Australia; Department of Psychiatry, School of Translational Medicine, Monash University, Level 4, 607 St Kilda Road, Melbourne, Victoria 3004, Australia.
Alfred Mental and Addiction Health, Alfred Health, Level 4, 607 St Kilda Road, Melbourne, Victoria 3004, Australia; Department of Psychiatry, School of Translational Medicine, Monash University, Level 4, 607 St Kilda Road, Melbourne, Victoria 3004, Australia.
J Affect Disord. 2025 Sep 15;385:119373. doi: 10.1016/j.jad.2025.05.033. Epub 2025 May 10.
Accelerated forms of repetitive transcranial magnetic stimulation (rTMS) are proving to be a safe and effective for treatment-resistant depression (TRD). However, the likelihood of treatment response remains difficult to predict. It is possible to assess inadequate treatment responses early in treatment courses to predict eventual non-response by course end.
Post-hoc analysis of prospective clinical trial data was conducted (N = 298). Participants were randomized to one of three treatment arms: daily, unilateral 10 Hz rTMS to the left dorsolateral prefrontal cortex or accelerated bilateral theta-burst stimulation (TBS) at either 80 % or 120 % resting motor threshold stimulation intensity. Clinical response was assessed using the Quick Inventory of Depressive Symptomatology (QIDS). Negative predictive values (NPVs) were generated at week 1 using various QIDS percentage improvement cut-offs to predict eventual non-response.
Participants who showed a ≤ 10 % or ≤ 20 % improvement in QIDS score by week 1 had NPVs ranging from 70.0 % to 97.5 %. Higher NPVs were found for participants randomized to low-intensity accelerated TBS than 10 Hz daily rTMS at week 1.
Accelerated TBS and standard rTMS courses featured relatively short courses of 20 sessions. Analyses predict eventual treatment response using only change in QIDS severity without subscale analysis.
Early treatment non-response potentially has predictive utility, including in an accelerated TBS protocol. Further studies should determine whether there is clinical benefit in reviewing and/or adapting treatment protocols in view of these findings.
重复经颅磁刺激(rTMS)的加速形式已被证明对难治性抑郁症(TRD)是安全有效的。然而,治疗反应的可能性仍然难以预测。在治疗过程早期评估治疗反应不足,以预测疗程结束时最终的无反应情况是可行的。
对前瞻性临床试验数据进行事后分析(N = 298)。参与者被随机分配到三个治疗组之一:每日对左侧背外侧前额叶皮质进行单侧10Hz rTMS,或在静息运动阈值刺激强度的80%或120%下进行加速双侧theta爆发刺激(TBS)。使用抑郁症状快速量表(QIDS)评估临床反应。在第1周使用各种QIDS改善百分比临界值生成阴性预测值(NPV),以预测最终的无反应情况。
到第1周时,QIDS评分改善≤10%或≤20%的参与者的NPV范围为70.0%至97.5%。在第1周,随机分配到低强度加速TBS组的参与者的NPV高于每日10Hz rTMS组。
加速TBS和标准rTMS疗程的疗程相对较短,为20次。分析仅使用QIDS严重程度的变化来预测最终治疗反应,未进行分量表分析。
早期治疗无反应可能具有预测效用,包括在加速TBS方案中。进一步的研究应确定鉴于这些发现,在审查和/或调整治疗方案时是否有临床益处。