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抗抑郁药治疗伴有重性抑郁障碍的儿童和青少年及安慰剂反应的影响:一项荟萃分析。

Antidepressants in children and adolescents with major depressive disorder and the influence of placebo response: A meta-analysis.

机构信息

Clinical Trials Network and Institute, Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

Clinical Trials Network and Institute, Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

出版信息

J Affect Disord. 2022 May 15;305:55-64. doi: 10.1016/j.jad.2022.02.074. Epub 2022 Mar 3.

Abstract

BACKGROUND

There are few available antidepressants for pediatric Major Depressive Disorder (MDD). The objective of this systematic review and meta-analysis was to review industry-funded studies of antidepressants in children and adolescents with MDD, and to better understand the contribution of study design and placebo response to the findings of these studies.

METHODS

Randomized, double-blind, placebo-controlled clinical trials that compared antidepressant with placebo for the acute treatment of MDD in children and/or adolescents were selected. Estimates of the standardized mean difference (SMD) in change in Children's Depression Rating Scale-Revised scores were pooled, after examining for heterogeneity. A random-effects meta-analysis was completed.

RESULTS

Thirty-four antidepressant-placebo comparisons, involving 6161 subjects, were included. The SMD among all studies was 0.12 (CI 0.08, 0.17; p < 0.001), a very small effect size, lower than that seen in studies of adults with MDD. When the meta-analysis was limited to studies with a low mean placebo response, the SMD increased to 0.19 and further increased to 0.22 when studies with at least a 50% chance of receiving placebo were included.

LIMITATIONS

Many studies focused on older children and younger adolescents. Our findings may not reflect antidepressant efficacy in older adolescents.

CONCLUSIONS

The modest SMD identified in this analysis may reflect study design factors and the application of antidepressants developed for adults to pediatric patients. Given the urgent clinical need for more pediatric MDD treatments, the influence of placebo response and the need for drug development tailored to this population should be considered in pediatric MDD trial design.

摘要

背景

目前用于儿童重度抑郁症(MDD)的抗抑郁药有限。本系统评价和荟萃分析的目的是回顾抗抑郁药治疗儿童和青少年 MDD 的行业资助研究,并更好地了解研究设计和安慰剂反应对这些研究结果的贡献。

方法

选择了比较抗抑郁药与安慰剂治疗儿童和/或青少年 MDD 急性治疗的随机、双盲、安慰剂对照临床试验。在检查异质性后,汇总了儿童抑郁评定量表修订版评分变化的标准化均数差(SMD)估计值。完成了随机效应荟萃分析。

结果

纳入了 34 项抗抑郁药与安慰剂的比较,涉及 6161 名受试者。所有研究的 SMD 为 0.12(CI 0.08, 0.17;p < 0.001),这是一个非常小的效应量,低于成人 MDD 研究中的效应量。当荟萃分析仅限于安慰剂反应平均值较低的研究时,SMD 增加到 0.19,当纳入至少有 50%接受安慰剂机会的研究时,SMD 进一步增加到 0.22。

局限性

许多研究都集中在年龄较大的儿童和较年轻的青少年上。我们的发现可能无法反映抗抑郁药在年龄较大的青少年中的疗效。

结论

本分析中确定的适度 SMD 可能反映了研究设计因素以及将为成人开发的抗抑郁药应用于儿科患者。鉴于儿科 MDD 治疗的迫切临床需求,应在儿科 MDD 试验设计中考虑安慰剂反应的影响和针对该人群的药物开发需求。

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