Cohen Sem E, de Boer Anthonius, Storosum Bram W C, Mattila Taina K, Niemeijer Marisa J, Geller Daniel A, Denys Damiaan, Zantvoord Jasper B
Amsterdam University Medical Center, Amsterdam, the Netherlands; Amsterdam Neuroscience Research Institute, Amsterdam, the Netherlands.
Medicines Evaluation Board, Utrecht, the Netherlands; Utrecht University, Utrecht, the Netherlands.
J Am Acad Child Adolesc Psychiatry. 2025 Jan 10. doi: 10.1016/j.jaac.2025.01.001.
Selective serotonin reuptake inhibitors (SSRIs) are the first choice in pharmacotherapy for children and adolescents with obsessive-compulsive disorder (OCD). SSRI trials for pediatric OCD have not been investigated using individual participant data (IPD), which is crucial for detecting patient-level effect modifiers. This study performed an IPD meta-analysis of efficacy of SSRIs compared with placebo and a meta-regression on baseline patient characteristics that might modify efficacy.
Crude participant data from short-term, randomized, placebo-controlled SSRI trials for pediatric OCD were obtained from the registry of the Dutch regulatory authority. A systematic literature search was also performed, and authors were approached to provide IPD. A 1- and 2-stage analysis was conducted, with change on Children's Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) as the primary outcome. Odds ratio (OR) with ≥35% CY-BOCS reduction was used as the responder outcome measure. Modifying effect of age, sex, weight, duration of illness, family history, and baseline symptom severity was examined. The Cochrane RoB 2.0 tool was used to examine methodological rigor, and Grading of Recommendations Assessment, Development, and Evaluation (GRADE) was used to examine certainty of evidence.
Data were obtained from 4 studies comprising 614 patients. The sample represented 86% of all participants ever included in double-blind placebo-controlled SSRI trials for pediatric OCD. Meta-analysis showed reduction of 3.0 CY-BOCS points compared with placebo (95% CI 2.5-3.5), corresponding to a small effect size (0.38 Hedges' g). Analysis of response showed an odds ratio of 1.89 (95% CI 1.45-2.45). Of all possible modifiers, severity was correlated negatively with odds ratio for response (β = -0.92, p = .0074). Risk of bias was generally low. All studies were performed in North America with an overrepresentation of White participants. Findings were limited by inability to include data on additional variables such as socioeconomic status and comorbidities.
This IPD meta-analysis showed a small effect size of SSRIs in pediatric OCD, with baseline severity as a negative modifier of response. Generalizability of findings might be limited by selective inclusion of White, North American participants.
Patient Characteristics and Efficacy of SSRI Treatment in Children and Adolescents With Obsessive Compulsive Disorder: An Individual Participant Data Meta-analysis of Randomized, Placebo-Controlled Trials; https://www.crd.york.ac.uk; CRD42023486079.
选择性5-羟色胺再摄取抑制剂(SSRIs)是治疗儿童及青少年强迫症(OCD)的药物治疗首选。尚未采用个体参与者数据(IPD)对儿科强迫症的SSRI试验进行研究,而IPD对于检测患者水平的效应修饰因素至关重要。本研究对SSRI与安慰剂相比的疗效进行了IPD荟萃分析,并对可能影响疗效的基线患者特征进行了荟萃回归分析。
从荷兰监管机构的登记处获取儿科强迫症短期、随机、安慰剂对照SSRI试验的原始参与者数据。还进行了系统的文献检索,并联系作者以提供IPD。进行了1阶段和2阶段分析,以儿童耶鲁-布朗强迫症量表(CY-BOCS)的变化作为主要结局。以CY-BOCS降低≥35%的比值比(OR)作为反应结局指标。研究了年龄、性别、体重、病程、家族史和基线症状严重程度的修饰作用。使用Cochrane RoB 2.0工具检查方法的严谨性,并使用推荐分级评估、制定和评价(GRADE)来检查证据的确定性。
数据来自4项研究,共614例患者。该样本占所有纳入儿科强迫症双盲安慰剂对照SSRI试验参与者的86%。荟萃分析显示,与安慰剂相比,CY-BOCS评分降低了3.0分(95%CI 2.5-3.5),对应较小的效应量(0.38 Hedges' g)。反应分析显示比值比为1.89(95%CI 1.45-2.45)。在所有可能的修饰因素中,严重程度与反应比值比呈负相关(β = -0.92,p = 0.0074)。偏倚风险一般较低。所有研究均在北美进行,白人参与者占比过高。由于无法纳入社会经济地位和合并症等其他变量的数据,研究结果受到限制。
这项IPD荟萃分析显示,SSRI在儿科强迫症中的效应量较小,基线严重程度是反应的负性修饰因素。研究结果的普遍性可能因选择性纳入北美白人参与者而受到限制。
《患强迫症儿童和青少年中SSRI治疗的患者特征和疗效:一项随机、安慰剂对照试验的个体参与者数据荟萃分析》;https://www.crd.york.ac.uk;CRD42023486079。