TY - JOUR
T1 - Comparisons of Accelerated Continuous and Intermittent Theta Burst Stimulation for Treatment-Resistant Depression and Suicidal Ideation
AU - Zhao, Haoyang
AU - Jiang, Chaonan
AU - Zhao, Miaomiao
AU - Ye, Yang
AU - Yu, Liang
AU - Li, Ying
AU - Luan, Honglin
AU - Zhang, Shiyi
AU - Xu, Pengfeng
AU - Chen, Xuanqiang
AU - Pan, Fen
AU - Shang, Desheng
AU - Hu, Xiaohan
AU - Jin, Kangyu
AU - Chen, Jingkai
AU - Mou, Tingting
AU - Hu, Shaohua
AU - Fitzgibbon, Bernadette M.
AU - Fitzgerald, Paul B.
AU - Cash, Robin F.H.
AU - Che, Xianwei
AU - Huang, Manli
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (Grant No. 82271562 [to MH]), the Key Research and Development Program of Zhejiang Province of China (Grant No. 2023C03077 [to MH]), and the Natural Science Foundation of Zhejiang Province of China (Grant No. LQ22H090005 [to FP]). The funding sources had no role in the study design; collection, analysis, and interpretation of data; writing of the manuscript; or decision to submit the paper for publication. HZ and CJ drafted the manuscript. MH, XChe, and SH participated in the design of this study. HZ, CJ, MZ, YY, KJ, YL, SZ, PX, FP, TM, XH, XChen, LY, and HL carried out the study and collected important background information. JC performed TBS treatments, and DS performed the MRI scan. HZ, YY, DS, and JC performed the statistical analysis. MH, FP, XChe, RFHC, BMF, and PBF revised the manuscript. All authors read the final manuscript. All authors contributed to the article and approved the submitted version. We gratefully acknowledge all the study participants. The raw data supporting the conclusions of this article will be made available by the corresponding author upon reasonable request. The authors report no biomedical financial interests or potential conflicts of interest.
Funding Information:
This work was supported by the National Natural Science Foundation of China (Grant No. 82271562 [to MH]), the Key Research and Development Program of Zhejiang Province of China (Grant No. 2023C03077 [to MH]), and the Natural Science Foundation of Zhejiang Province of China (Grant No. LQ22H090005 [to FP]). The funding sources had no role in the study design; collection, analysis, and interpretation of data; writing of the manuscript; or decision to submit the paper for publication.
Publisher Copyright:
© 2023 Society of Biological Psychiatry
PY - 2024/7
Y1 - 2024/7
N2 - Background: Suicidal ideation is a substantial clinical challenge in treatment-resistant depression (TRD). Recent work demonstrated promising antidepressant effects in TRD patients with no or mild suicidal ideation using a specific protocol termed intermittent theta burst stimulation (iTBS). Here, we examined the clinical effects of accelerated schedules of iTBS and continuous TBS (cTBS) in patients with moderate to severe suicidal ideation. Methods: Patients with TRD and moderate to severe suicidal ideation (n = 44) were randomly assigned to receive accelerated iTBS or cTBS treatment. Treatments were delivered in 10 daily TBS sessions (1800 pulses/session) for 5 consecutive days (total of 90,000 pulses). Neuronavigation was employed to target accelerated iTBS and cTBS to the left and right dorsolateral prefrontal cortex (DLPFC), respectively. Clinical outcomes were evaluated in a 4-week follow-up period. Results: Accelerated cTBS was superior to iTBS in the management of suicidal ideation (pweek 1 = .027) and anxiety symptoms (pweek 1 = .01). Accelerated iTBS and cTBS were comparable in antidepressant effects (p < .001; accelerated cTBS: mean change at weeks 1, 3, 5 = 49.55%, 54.99%, 53.11%; accelerated iTBS: mean change at weeks 1, 3, 5 = 44.52%, 48.04%, 51.74%). No serious adverse events occurred during the trial. One patient withdrew due to hypomania. The most common adverse event was discomfort at the treatment site (22.73% in both groups). Conclusions: These findings provide the first evidence that accelerated schedules of left DLPFC iTBS and right DLPFC cTBS are comparably effective in managing antidepressant symptoms and indicate that right DLPFC cTBS is potentially superior in reducing suicidal ideation and anxiety symptoms.
AB - Background: Suicidal ideation is a substantial clinical challenge in treatment-resistant depression (TRD). Recent work demonstrated promising antidepressant effects in TRD patients with no or mild suicidal ideation using a specific protocol termed intermittent theta burst stimulation (iTBS). Here, we examined the clinical effects of accelerated schedules of iTBS and continuous TBS (cTBS) in patients with moderate to severe suicidal ideation. Methods: Patients with TRD and moderate to severe suicidal ideation (n = 44) were randomly assigned to receive accelerated iTBS or cTBS treatment. Treatments were delivered in 10 daily TBS sessions (1800 pulses/session) for 5 consecutive days (total of 90,000 pulses). Neuronavigation was employed to target accelerated iTBS and cTBS to the left and right dorsolateral prefrontal cortex (DLPFC), respectively. Clinical outcomes were evaluated in a 4-week follow-up period. Results: Accelerated cTBS was superior to iTBS in the management of suicidal ideation (pweek 1 = .027) and anxiety symptoms (pweek 1 = .01). Accelerated iTBS and cTBS were comparable in antidepressant effects (p < .001; accelerated cTBS: mean change at weeks 1, 3, 5 = 49.55%, 54.99%, 53.11%; accelerated iTBS: mean change at weeks 1, 3, 5 = 44.52%, 48.04%, 51.74%). No serious adverse events occurred during the trial. One patient withdrew due to hypomania. The most common adverse event was discomfort at the treatment site (22.73% in both groups). Conclusions: These findings provide the first evidence that accelerated schedules of left DLPFC iTBS and right DLPFC cTBS are comparably effective in managing antidepressant symptoms and indicate that right DLPFC cTBS is potentially superior in reducing suicidal ideation and anxiety symptoms.
KW - DLPFC
KW - Suicidal ideation
KW - Theta burst stimulation
KW - Treatment-resistant depression
UR - http://www.scopus.com/inward/record.url?scp=85186184880&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2023.12.013
DO - 10.1016/j.biopsych.2023.12.013
M3 - Article
C2 - 38142717
AN - SCOPUS:85186184880
SN - 0006-3223
VL - 96
SP - 26
EP - 33
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 1
ER -