Trajectories of Irritability Improvement in Depressed Adolescents Treated With 1 Hz and 10 Hz Transcranial Magnetic Stimulation.

IF 4.5 2区 医学 Q1 PSYCHIATRY
Karina Delaney, Paul A Nakonezny, Dicle Buyuktaskin, Lucero Sangster Carrasco, Arjun P Athreya, Magdalena Romanowicz, Julia Shekunov, Jennifer L Vande Voort, Paul E Croarkin
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引用次数: 0

Abstract

Objective: Irritability is a debilitating, transdiagnostic symptom in adolescents spanning internalizing and externalizing disorders, and early reduction in irritability with antidepressant treatments has been seen as a positive prognostic sign in depression recovery. There are substantial knowledge gaps regarding how transcranial magnetic stimulation (TMS) treatments impact irritability.

Methods: This exploratory study sought to investigate the relationship between irritability and depressive symptoms in adolescents with a DSM-5 diagnosis of major depressive disorder (MDD) undergoing treatment with 2 different doses of TMS. Participants aged 12-18 years (N = 41) underwent 6 weeks of treatment (30 sessions) in a double-blind, randomized trial of 1 Hz vs. 10 Hz TMS for the treatment of MDD. The clinical trial was conducted from September 24, 2018, through March 3, 2023. A linear mixed model was used to assess the change in irritability (assessed with item 8 on the Children's Depression Rating Scale Revised) throughout the treatment course, and a logistic regression was implemented to examine the relationship between early (week 4) irritability improvements and a posttreatment Clinical Global Impressions-Improvement (CGI-I) score.

Results: Irritability significantly improved during the course of TMS treatments in conjunction with overall depression improvement across the 6 week trial for the 1 Hz TMS group (P = .0120, d =0.381) and for the 10 Hz TMS group (P = .0288, d = 0.331). There was a significant negative (inverse) relationship between the change in irritability symptoms and CGI-I response for the 10 Hz TMS group (δ log odds = -1.5474, SE = 0.7343, P = .0351) and for the 1 Hz TMS group (δ log odds = -1.2852, SE = 0.5656, P = .0231).

Conclusion: These results suggest that irritability is an important correlate of disease severity and predictor of treatment response for MDD in adolescents, replicating similar results found in trials using antidepressant medications. Future research should focus on incorporating assessments of irritability into clinical decision-making and intervention discovery for transdiagnostic symptoms of irritability in youth and adolescents.

Clinical Trial Registration: Data used in this secondary analysis came from ClinicalTrials.gov identifier: NCT03363919.

接受1hz和10hz经颅磁刺激治疗的抑郁青少年易怒改善轨迹。
目的:易怒是青少年内化和外化障碍的一种使人衰弱的跨诊断症状,抗抑郁药物治疗早期减少易怒被视为抑郁症康复的积极预后迹象。关于经颅磁刺激(TMS)治疗如何影响烦躁,存在大量的知识空白。方法:本探索性研究旨在探讨DSM-5诊断为重度抑郁症(MDD)的青少年在接受两种不同剂量的经颅刺激治疗后,烦躁与抑郁症状之间的关系。12-18岁的参与者(N = 41)在一项1hz vs 10hz TMS治疗重度抑郁症的双盲随机试验中接受了6周(30个疗程)的治疗。该临床试验于2018年9月24日至2023年3月3日进行。采用线性混合模型评估整个治疗过程中易怒的变化(使用修订儿童抑郁评定量表第8项进行评估),并采用逻辑回归来检验早期(第4周)易怒改善与治疗后临床总体印象改善(CGI-I)评分之间的关系。结果:在为期6周的试验中,1 Hz TMS组和10 Hz TMS组的烦躁性显著改善,同时抑郁症总体改善(P = 0.0120, d =0.381)。10 Hz经颅磁刺激组和1 Hz经颅磁刺激组的激惹症状变化与CGI-I反应呈显著负相关(δ log odds = -1.5474, SE = 0.7343, P = 0.051), δ log odds = -1.2852, SE = 0.5656, P = 0.0231)。结论:这些结果表明,易怒是疾病严重程度的重要相关因素,也是青少年MDD治疗反应的预测因素,与使用抗抑郁药物的试验结果相似。未来的研究应侧重于将易怒评估纳入青少年易怒跨诊断症状的临床决策和干预措施的发现。临床试验注册:本次要分析使用的数据来自ClinicalTrials.gov识别码:NCT03363919。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Psychiatry
Journal of Clinical Psychiatry 医学-精神病学
CiteScore
7.40
自引率
1.90%
发文量
0
审稿时长
3-8 weeks
期刊介绍: For over 75 years, The Journal of Clinical Psychiatry has been a leading source of peer-reviewed articles offering the latest information on mental health topics to psychiatrists and other medical professionals.The Journal of Clinical Psychiatry is the leading psychiatric resource for clinical information and covers disorders including depression, bipolar disorder, schizophrenia, anxiety, addiction, posttraumatic stress disorder, and attention-deficit/hyperactivity disorder while exploring the newest advances in diagnosis and treatment.
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