Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, IiSGM, School of Medicine, Universidad Complutense, CIBERSAM. Madrid, Spain.
Department of Child and Adolescent Psychiatry, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Schizophr Bull. 2019 Jan 1;45(1):57-68. doi: 10.1093/schbul/sbx192.
We conducted a meta-regression analysis of all double-blind, randomized, placebo-controlled clinical trials (DBRCTs) reporting effects of drug and placebo on negative symptoms in people with stable schizophrenia and predominant or prominent negative symptoms to assess predictors of placebo response in these individuals. We used Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines for systematic reviews and meta-analyses to conduct a systematic literature search to identify DBRCTs assessing treatment efficacy on negative symptoms, as primary outcome, in patients with stable schizophrenia and predominant or prominent negative symptoms. We used Cohen's d, with 95% CIs, as the effect size measure for placebo response, based on negative symptom change scores from baseline to endpoint (range 4 to 24 wk) in the placebo-treated group. We included 18 DBRCTs from 17 publications, assessing the effect of 13 drugs vs placebo on negative symptoms and comprising 998 patients, in the meta-regression analyses. Overall, drugs showed greater efficacy than placebo in reducing negative symptoms, with small effect size (Cohen's d: 0.208, P = .020). Placebo response was significant (P < .001) and clinically relevant (Cohen's d: 2.909), but there was significant heterogeneity and high risk of publication bias. Multivariable meta-regression analyses showed that larger numbers of arms in the trial, larger numbers of study sites and industry sponsorship were significant moderators of placebo response in this population. Our results suggest that some clinical trial design and operational factors affect the level of placebo response in such studies, thus highlighting the need for designs better suited to assess these outcomes.
我们对所有报告药物和安慰剂对稳定精神分裂症和主要或突出阴性症状患者阴性症状影响的双盲、随机、安慰剂对照临床试验(DBRCT)进行了荟萃回归分析,以评估这些个体中安慰剂反应的预测因素。我们使用系统评价和荟萃分析的首选报告项目(PRISMA)指南进行系统文献检索,以确定评估稳定精神分裂症和主要或突出阴性症状患者阴性症状作为主要结局的 DBRCT 治疗效果。我们使用 Cohen's d(95%CI)作为安慰剂反应的效应量测量,基于安慰剂治疗组从基线到终点(范围 4 至 24 周)的阴性症状变化评分。我们纳入了来自 17 篇文献的 18 项 DBRCT,评估了 13 种药物与安慰剂对阴性症状的影响,包括 998 名患者,用于荟萃回归分析。总体而言,药物在减轻阴性症状方面比安慰剂更有效,效应量较小(Cohen's d:0.208,P =.020)。安慰剂反应显著(P <.001)且具有临床意义(Cohen's d:2.909),但存在显著的异质性和高发表偏倚风险。多变量荟萃回归分析表明,试验中的试验臂数量较多、研究地点数量较多和行业赞助是该人群中安慰剂反应的显著调节剂。我们的研究结果表明,一些临床试验设计和操作因素会影响此类研究中安慰剂反应的水平,因此强调需要设计更适合评估这些结果的设计。