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

被引:29
作者
Farokhnia, Mehdi [1 ]
Sabzabadi, Maryam [1 ]
Pourmahmoud, Hossein [2 ]
Khodaie-Ardakani, Mohammad-Reza [2 ]
Hosseini, Seyed-Mohammad-Reza [1 ]
Yekehtaz, Habibeh [1 ]
Tabrizi, Mina [3 ]
Rezaei, Farzin [4 ]
Salehi, Bahman [5 ]
Akhondzadeh, Shahin [1 ]
机构
[1] Univ Tehran Med Sci, Roozbeh Hosp, Psychiat Res Ctr, Tehran 13337, Iran
[2] Univ Social Welf & Rehabil Sci, Razi Hosp, Tehran, Iran
[3] Univ Tehran Med Sci, Fac Med, Dept Med Genet, Tehran 13337, Iran
[4] Kurdistan Univ Med Sci, Dept Psychiat, Sanandaj, Iran
[5] Arak Univ Med Sci, Dept Psychiat, Arak, Iran
关键词
Riluzole; Glutamate; Schizophrenia; Negative symptoms; PANSS; Clinical trial; OPEN-LABEL TRIAL; GLUTAMATE ANTAGONIST; DOPAMINE RELEASE; AGENT RILUZOLE; RATING-SCALE; ADD-ON; PHENCYCLIDINE; LAMOTRIGINE; DYSFUNCTION; MECHANISMS;
D O I
10.1007/s00213-013-3261-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several recent studies have focused on glutamate modulating agents for symptoms relief in schizophrenia, especially negative symptoms which are resistant to conventional therapies. 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. In this randomized double-blind placebo-controlled parallel-group study, 50 patients with chronic schizophrenia and a score of a parts per thousand yen20 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. 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 (beta = -0.56, P < 0.001). No significant difference was observed between two groups in the frequency of side effects. 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. Iranian registry of clinical trials www.irct.ir, IRCT201107281556N26.
引用
收藏
页码:533 / 542
页数:10
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