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精神分裂症谱系障碍中抗精神病药物治疗的副作用变异性研究:方差的荟萃分析。

Examining Side Effect Variability of Antipsychotic Treatment in Schizophrenia Spectrum Disorders: A Meta-analysis of Variance.

机构信息

University Hospital of Psychiatry Zurich, Zurich, Switzerland.

Center for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, NY, USA.

出版信息

Schizophr Bull. 2021 Oct 21;47(6):1601-1610. doi: 10.1093/schbul/sbab078.

Abstract

Side effects of antipsychotic drugs play a key role in nonadherence of treatment in schizophrenia spectrum disorders (SSD). While clinical observations suggest that side effect variability between patients may be considerable, statistical evidence is required to confirm this. Here, we hypothesized to find larger side effect variability under treatment compared with control. We included double-blind, placebo-controlled, randomized controlled trials (RCTs) of adults with a diagnosis of SSD treated with 1 out of 14 antipsychotics. Standard deviations of the pre-post treatment differences of weight gain, prolactin levels, and corrected QT (QTc) times were extracted. The outcome measure was the variability ratio of treatment to control for individual antipsychotic drugs and the overall variability ratio of treatment to control across RCTs. Individual variability ratios were weighted by the inverse-variance method and entered into a random-effects model. We included N = 16 578 patients for weight gain, N = 16 633 patients for prolactin levels, and N = 10 384 patients for QTc time. Variability ratios (VR) were significantly increased for weight gain (VR = 1.08; 95% CI: 1.02-1.14; P = .004) and prolactin levels (VR = 1.38; 95% CI: 1.17-1.62; P < .001) but did not reach significance for QTc time (VR = 1.05; 95% CI: 0.98-1.12; P = 0.135). We found marked differences between individual antipsychotics and increased variability in side effects in patients under treatment with antipsychotics suggesting that subgroups of patients or individual patients may benefit from treatment allocation through stratified or personalized medicine.

摘要

抗精神病药物的副作用在精神分裂症谱系障碍(SSD)的治疗不依从中起着关键作用。虽然临床观察表明患者之间的副作用变异性可能相当大,但需要统计证据来证实这一点。在这里,我们假设在治疗下会比对照下发现更大的副作用变异性。我们纳入了 14 种抗精神病药物之一治疗成人 SSD 的双盲、安慰剂对照、随机对照试验(RCT)。体重增加、催乳素水平和校正 QT(QTc)时间的治疗前后差异的标准差被提取。测量结果是个体抗精神病药物治疗与对照的变异性比和 RCT 中治疗与对照的总体变异性比。个体变异性比通过逆方差法加权,并纳入随机效应模型。我们纳入了 N = 16578 例体重增加患者、N = 16633 例催乳素水平患者和 N = 10384 例 QTc 时间患者。体重增加的变异性比(VR)显著增加(VR = 1.08;95%CI:1.02-1.14;P =.004)和催乳素水平(VR = 1.38;95%CI:1.17-1.62;P <.001),但 QTc 时间未达到显著水平(VR = 1.05;95%CI:0.98-1.12;P = 0.135)。我们发现个体抗精神病药物之间存在显著差异,并且接受抗精神病药物治疗的患者的副作用变异性增加,这表明亚组患者或个体患者可能受益于通过分层或个体化医学进行的治疗分配。

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