Effect of Lurasidone on Social Functioning in Schizophrenia: Post Hoc Analysis of the JEWEL Study.

Itaru Miura, Fumiya Sano, Reiko Sakaguchi, Keisuke Okamoto, Hidenori Maruyama
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Abstract

Objective: To evaluate the effects of lurasidone on social functioning in schizophrenia over the course of a 6-week, double-blind, placebo-controlled study and a subsequent 12-week open-label extension study. Methods: A total of 478 patients with schizophrenia (per DSM-IV-TR criteria) randomized to either lurasidone 40 mg/d (n = 245) or placebo (n = 233) in the initial 6-week double-blind study (initiated May 2016, completed November 2018) were included in the analysis. Longer-term changes were examined in a sample of 146 patients who received lurasidone, and 141 who received placebo, during the 6-week study and received flexibly dosed (40-80 mg/d) lurasidone during the 12-week extension phase. The 4-item Positive and Negative Syndrome Scale (PANSS) prosocial subscale was used to examine changes in social functioning. Results: At week 6 of the double-blind phase, lurasidone-treated patients had significantly greater improvement on the PANSS prosocial subscale compared to placebo-treated patients (P < .01, effect size at week 6 = 0.33). Significant differences from placebo were also evident at week 2 (P < .05), week 4 (P < .001), and week 5 (P < .01). Across the 12-week extension phase, patients who received lurasidone during both the 6-week double-blind phase and the 12-week open-label phase continued to show successive decreases in scores on the 4-item PANSS prosocial subscale (score change of -3.0 from double-blind baseline to week 6; mean score change of -4.2 from double-blind baseline to week 12 of the extension phase). Conclusions: In patients with schizophrenia treated with lurasidone, social functioning improved relative to placebo during a 6-week double-blind study and continued to improve over the course of 12 weeks of extension treatment with lurasidone. Effects of lurasidone on social functioning appear to be comparable to what has been reported for other atypical antipsychotics. Trial Registration: EudraCT Numbers: 2016-000060-42 and 2016-000061-23.
鲁拉西酮对精神分裂症患者社会功能的影响:JEWEL研究的事后分析。
研究目的通过为期6周的双盲安慰剂对照研究和随后为期12周的开放标签扩展研究,评估鲁拉西酮对精神分裂症患者社会功能的影响。研究方法共有478名精神分裂症患者(根据DSM-IV-TR标准)被纳入分析,他们在最初的6周双盲研究(2016年5月启动,2018年11月完成)中被随机分配至鲁拉西酮40 mg/d(n = 245)或安慰剂(n = 233)。在为期6周的研究中,146名患者接受了鲁拉西酮治疗,141名患者接受了安慰剂治疗,并在为期12周的延长阶段接受了剂量灵活(40-80 mg/d)的鲁拉西酮治疗。研究使用了4个项目的积极与消极综合征量表(PANSS)亲社会分量表来考察患者社会功能的变化。研究结果在双盲阶段的第6周,与安慰剂治疗的患者相比,鲁拉西酮治疗的患者在PANSS亲社会分量表上有明显的改善(P < .01,第6周的效应大小= 0.33)。第2周(P <.05)、第4周(P <.001)和第5周(P <.01)与安慰剂相比也有明显差异。在为期12周的延长期中,在6周双盲期和12周开放标签期接受鲁拉西酮治疗的患者在4项PANSS亲社会分量表上的得分持续下降(从双盲基线到第6周的得分变化为-3.0;从双盲基线到延长期第12周的平均得分变化为-4.2)。结论在为期6周的双盲研究中,接受鲁拉西酮治疗的精神分裂症患者的社会功能相对于安慰剂有所改善,并且在鲁拉西酮延长治疗的12周期间仍在持续改善。鲁拉西酮对社会功能的影响似乎与其他非典型抗精神病药物相当。试验注册:EudraCT 编号2016-000060-42和2016-000061-23。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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