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阿莫达非尼辅助治疗对精神分裂症/分裂情感障碍患者抗精神病药物治疗后认知功能和精神病理学的影响:一项随机、双盲、安慰剂对照试验。

The effect of adjunctive armodafinil on cognitive performance and psychopathology in antipsychotic-treated patients with schizophrenia/schizoaffective disorder: a randomized, double-blind, placebo-controlled trial.

机构信息

Department of Psychiatry, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

Schizophr Res. 2011 Aug;130(1-3):106-13. doi: 10.1016/j.schres.2011.05.015. Epub 2011 Jun 8.

Abstract

BACKGROUND

The efficacy, safety and tolerability of adjunctive armodafinil for cognitive performance, and negative and affective symptoms, were examined in 60 patients with schizophrenia or schizoaffective disorder.

METHOD

This was a 6-week, double-blind, placebo-controlled, fixed dose trial of armodafinil (150 mg/d) augmentation in patients with clinically stable schizophrenia or schizoaffective disorder. Cognition, psychopathology, alertness/wakefulness and adverse effects were assessed with standardized rating instruments. The primary endpoint was performance on measures of attention/vigilance.

RESULTS

Patients were randomly allocated to adjunctive armodafinil or placebo. There was a significant Drug×Time interaction effect for attention/vigilance, due to modest non-significant worsening in the armodafinil group and improvement in the armodafinil group [CPT-Pairs d', F(1,40)=6.2, p=0.017]. However, it became non-significant after correction for multiple comparisons. There were no differences between armodafinil and placebo in other cognitive domains or psychopathology measures. However, armodafinil was associated with significant improvement in the Scale for the Assessment of Negative Symptoms (SANS) anhedonia-asociality [F(1,41)=4.1, p=0.05].

CONCLUSIONS

There were no significant differences in neurocognitive measures between adjunctive armodafinil and placebo in this 6-week study. Armodafinil improved anhedonia-asociality, but not other negative symptom domains.

摘要

背景

本研究旨在评估辅助阿莫达非尼治疗对认知表现、负性症状和情感症状的疗效、安全性和耐受性,共纳入 60 例精神分裂症或分裂情感障碍患者。

方法

这是一项为期 6 周的、双盲、安慰剂对照、固定剂量的临床试验,旨在评估阿莫达非尼(150mg/d)对临床稳定的精神分裂症或分裂情感障碍患者的增效作用。采用标准化评定量表评估认知功能、精神病理学、警觉性/觉醒度和不良反应。主要终点为注意力/警觉性评估指标的表现。

结果

患者随机分配至辅助阿莫达非尼或安慰剂组。注意力/警觉性存在显著的药物×时间交互作用效应,这主要是由于阿莫达非尼组出现了轻微的非显著性恶化,而阿莫达非尼组出现了改善[CPT-Pairs d',F(1,40)=6.2,p=0.017]。然而,经多重比较校正后,该差异无统计学意义。在其他认知领域或精神病理学评估指标上,阿莫达非尼与安慰剂之间无差异。然而,阿莫达非尼与显著改善阴性症状评定量表(SANS)快感缺失-社交退缩[F(1,41)=4.1,p=0.05]有关。

结论

在这项为期 6 周的研究中,辅助阿莫达非尼与安慰剂在神经认知评估指标上无显著差异。阿莫达非尼改善了快感缺失-社交退缩,但对其他阴性症状领域无影响。

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