Razi Psychiatric Hospital, Welfare Sciences University, Iran.
J Psychiatr Res. 2013 Apr;47(4):472-8. doi: 10.1016/j.jpsychires.2013.01.011. Epub 2013 Jan 30.
Some 5-HT3 antagonists such as ondansetron have shown beneficial effects on negative symptoms of patients with schizophrenia. We aimed to evaluate the efficacy of granisetron (another 5-HT3 antagonist) add-on therapy in the treatment of negative symptoms of patients with stable schizophrenia. In a randomized, double-blind, and placebo-controlled study, forty stable patients with schizophrenia (DSM-IV-TR), were randomized to either granisetron (1 mg twice daily) or placebo (twice daily) in addition to risperidone up to 6 mg/day for eight weeks. The patients were assessed using positive and negative syndrome scale (PANSS) and extrapyramidal symptom rating scale (ESRS) at baseline, week 4 and 8. Hamilton depression rating scale (HDRS) was used to assess depression at baseline and week 8. Thirty-eight patients completed the trial. Granisetron group showed a significantly greater improvement on negative subscale than the placebo group at endpoint [t(38) = 6.046, mean difference (±95% CI) = 3.2(1.8-3.7), P < 0.001]. The same effect was observed for total score [t(38) = 4.168, mean difference (95% CI) = 3.2(1.6-4.7), P < 0.001]. However the placebo and granisetron groups did not differ in their reduction of positive and general psychopathology symptoms scores. HDRS scores and its changes did not differ between the two groups. The ESRS score at week 4 was significantly lower in the granisetron than the placebo group while the two groups showed similar ESRS score at week 8. Frequency of other side effects was similar between the two groups. In summary, granisetron add-on can safely and effectively reduce the primary negative symptoms of patients with schizophrenia.
一些 5-HT3 拮抗剂,如昂丹司琼,已显示出对精神分裂症患者阴性症状的有益影响。我们旨在评估格拉司琼(另一种 5-HT3 拮抗剂)添加治疗对稳定精神分裂症患者阴性症状的疗效。在一项随机、双盲、安慰剂对照研究中,40 例稳定期精神分裂症患者(DSM-IV-TR)被随机分为格拉司琼(1mg,每日 2 次)或安慰剂(每日 2 次),同时加用利培酮至 6mg/天,共 8 周。患者在基线、第 4 周和第 8 周时使用阳性和阴性症状量表(PANSS)和锥体外系症状评定量表(ESRS)进行评估。在基线和第 8 周时使用汉密尔顿抑郁量表(HDRS)评估抑郁。38 例患者完成了试验。在终点时,格拉司琼组在阴性量表上的改善明显大于安慰剂组[t(38)=6.046,平均差异(±95%CI)=3.2(1.8-3.7),P<0.001]。总分也观察到相同的效果[t(38)=4.168,平均差异(95%CI)=3.2(1.6-4.7),P<0.001]。然而,安慰剂组和格拉司琼组在阳性和一般精神病症状评分的降低方面没有差异。两组 HDRS 评分及其变化无差异。格拉司琼组在第 4 周时的 ESRS 评分明显低于安慰剂组,而两组在第 8 周时的 ESRS 评分相似。两组的其他不良反应发生率相似。总之,格拉司琼添加治疗可以安全有效地减轻精神分裂症患者的主要阴性症状。