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A double-blind, placebo controlled, randomized trial of riluzole as an adjunct to risperidone for treatment of negative symptoms in patients with chronic schizophrenia

机译:利鲁唑作为利培酮的辅助治疗安慰剂对照的双盲,随机试验,用于治疗慢性精神分裂症患者的阴性症状

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Rationale: Several recent studies have focused on glutamate modulating agents for symptoms relief in schizophrenia, especially negative symptoms which are resistant to conventional therapies. Objectives: We aimed to assess the efficacy and tolerability of riluzole, an anti-glutamate agent with neuroprotective properties, as an adjunct to risperidone in improving negative symptoms of schizophrenia. Methods: In this randomized double-blind placebo-controlled parallel-group study, 50 patients with chronic schizophrenia and a score of ≥20 on the negative subscale of positive and negative syndrome scale (PANSS) were enrolled in the active phase of their illness. Participants were equally randomized to receive riluzole (100 mg/day) or placebo in addition to risperidone (up to 6 mg/day) for 8 weeks. Participants were rated by PANSS every 2 weeks. The primary outcome of this study was the difference in the decrease of PANSS negative subscale score from baseline to the study endpoint between the two groups. Results: By the study endpoint, riluzole-treated patients showed significantly greater improvement in the negative symptoms (P < 0.001) as well as the PANSS total and general psychopathology subscale scores (P = 0.001 and P < 0.001; respectively) compared to the placebo group. Treatment group was the only significant predictor of changes in negative symptom in this trial (β = -0.56, P < 0.001). No significant difference was observed between two groups in the frequency of side effects. Conclusion: These preliminary findings suggest that riluzole may be a safe and effective medication for the treatment of negative symptoms in patients with chronic schizophrenia. Further research and replication of study findings is warranted. Clinical trial registry name and registration number: Iranian registry of clinical trials www.irct.ir, IRCT201107281556N26
机译:理由:最近的一些研究集中在谷氨酸调节剂上,以减轻精神分裂症的症状,尤其是对常规疗法有抵抗力的阴性症状。目的:我们旨在评估具有神经保护特性的抗谷氨酸剂利鲁唑作为利培酮辅助改善精神分裂症阴性症状的功效和耐受性。方法:在这项随机双盲安慰剂对照平行组研究中,将50例慢性精神分裂症患者,其正负综合症量表的负子量表(PANSS)得分≥20。除利培酮(最多6 mg /天)外,参与者同样随机接受利鲁唑(100 mg /天)或安慰剂治疗8周。 PANSS每2周对参与者进行一次评分。这项研究的主要结局是两组之间从基线到研究终点的PANSS阴性子量表得分减少的差异。结果:与安慰剂相比,到研究终点,利鲁唑治疗的患者的阴性症状(P <0.001)以及PANSS总和一般心理病理学次级量表得分(P分别为0.001和P <0.001)均有显着改善。组。在该试验中,治疗组是阴性症状变化的唯一重要预测因子(β= -0.56,P <0.001)。两组之间在副作用发生频率上没有显着差异。结论:这些初步发现表明,利鲁唑可能是治疗慢性精神分裂症患者阴性症状的安全有效药物。进一步研究和复制研究结果是必要的。临床试验注册中心名称和注册号:伊朗临床试验注册中心www.irct.ir,IRCT201107281556N26

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