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提交用于成人强迫症监管审批的选择性5-羟色胺再摄取抑制剂安慰剂对照试验的个体患者数据荟萃分析。

Individual patient data meta-analysis of placebo-controlled trials of selective serotonin reuptake inhibitors submitted for regulatory approval in adult obsessive-compulsive disorder.

作者信息

Cohen Sem E, Storosum Bram W, Zantvoord Jasper B, Mattila Taina K, de Boer Anthonius, Denys Damiaan

机构信息

Department of Psychiatry, Amsterdam UMC, Amsterdam, Netherlands.

Amsterdam Neuroscience Research Institute, Amsterdam, Netherlands.

出版信息

Br J Psychiatry. 2025 May 15:1-8. doi: 10.1192/bjp.2025.87.

Abstract

BACKGROUND

Selective serotonin reuptake inhibitors (SSRIs) are the preferred pharmacological treatment for obsessive-compulsive disorder (OCD). However, insufficient response is common and it remains unclear whether specific patient-level factors influence the likelihood of treatment response.

AIMS

To determine the efficacy and acceptability of SSRIs in adult OCD, and to identify patient-level modifiers of efficacy.

METHODS

We conducted an individual patient data meta-analysis (IPDMA) of industry-sponsored short-term, randomised, placebo-controlled SSRI trials submitted for approval to the Dutch regulatory agency to obtain marketing approval for treating OCD in adults. We performed a two-stage meta-analysis, using crude data of available trials. The primary outcome was the difference in Yale-Brown Obsessive-Compulsive Scale (YBOCS) change between active treatment and placebo. Secondary outcomes were differences in response (defined as the odds ratio of ≥35% YBOCS point reduction) and acceptability (defined as the odds ratio for all-cause discontinuation). We examined the modifying effect of baseline characteristics: age, gender, illness severity, depressive symptoms, weight, illness duration and history of antidepressant use.

RESULTS

After excluding three trials because of missing data, we analysed results from 11 trials (79% of all submitted trials, = 2372). The trial duration ranged from 10 to 13 weeks. Mean difference of SSRIs relative to placebo was 2.65 YBOCS points (95% CI 1.85-3.46, < 0.0001), equalling a small effect size (0.33 Hedges' ). The odds ratio for response was 2.21 in favour of active treatment (95% CI 1.72-2.83, < 0.0001), with a number needed to treat of seven. Patient characteristics did not modify symptom change or response. Acceptability was comparable for SSRIs and placebo.

CONCLUSIONS

Our IPDMA showed that SSRIs are well accepted and superior to placebo for treating OCD. The effects are modest and independent of baseline patient characteristics.

摘要

背景

选择性5-羟色胺再摄取抑制剂(SSRIs)是强迫症(OCD)的首选药物治疗方法。然而,疗效欠佳的情况很常见,目前尚不清楚特定的患者层面因素是否会影响治疗反应的可能性。

目的

确定SSRIs在成人强迫症治疗中的疗效和可接受性,并识别疗效的患者层面调节因素。

方法

我们对制药行业赞助的短期、随机、安慰剂对照的SSRI试验进行了个体患者数据荟萃分析(IPDMA),这些试验已提交给荷兰监管机构以获得治疗成人强迫症的上市许可。我们使用现有试验的原始数据进行了两阶段荟萃分析。主要结局是活性治疗组与安慰剂组之间耶鲁-布朗强迫症量表(YBOCS)变化的差异。次要结局是反应差异(定义为YBOCS评分降低≥35%的比值比)和可接受性(定义为全因停药的比值比)。我们研究了基线特征的调节作用:年龄、性别、疾病严重程度、抑郁症状、体重、病程和抗抑郁药使用史。

结果

由于数据缺失排除三项试验后,我们分析了11项试验的结果(占所有提交试验的79%,n = 2372)。试验持续时间为10至13周。SSRIs相对于安慰剂的平均差异为2.65个YBOCS评分(95%CI 1.85 - 3.46,P < 0.0001),相当于小效应量(0.33 Hedges'g)。活性治疗组反应的比值比为2.21(95%CI 1.72 -

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