Department of Psychiatry, Dow University of Health Sciences, Karachi, Pakistan.
Ziauddin University Hospital, Karachi, Pakistan.
J Psychopharmacol. 2024 Sep;38(9):818-826. doi: 10.1177/02698811241267836. Epub 2024 Sep 5.
Variable benefits have been reported from the adjunctive use of simvastatin and the 5HT3 receptor antagonist, ondansetron, in patients with schizophrenia. We investigated their independent efficacy and possible synergy to improve negative symptoms of schizophrenia within a single trial.
A 6-month, randomised, double-blind, placebo-controlled trial with a 4-arm, 2 × 2 factorial design, in three centres in Pakistan. In total, 303 people with stable treated schizophrenia aged 18-65 were randomly allocated to add-on ondansetron, simvastatin, both or neither. The primary outcome was a Positive and Negative Syndrome Scale (PANSS) negative score at 3 and 6 months.
Mixed model analysis and analysis of covariance revealed no main effects of simvastatin or ondansetron but a significant negative interaction between them ( = 0.03); when given alone, both drugs significantly reduced negative symptoms compared to placebo but they were ineffective in combination. Individual treatment effects versus placebo were -1.9 points (95%CIs -3.23, -0.49; = 0.01) for simvastatin and -1.6 points for ondansetron (95%CIs -3.00, -0.14; = 0.03). Combined treatment significantly increased depression and side effects. In those with less than the median 5 years of treatment, ondansetron improved all PANSS subscales, global functioning measures and verbal learning and fluency, whereas simvastatin did not.
Small improvement in negative symptoms on simvastatin and ondansetron individually are not synergistic in combination in treating negative symptoms of schizophrenia. Ondansetron showed broad efficacy in patients on stable antipsychotic treatment within 5 years of illness. The findings suggest that ondansetron should be evaluated in patients at risk of psychosis or early in treatment.
在精神分裂症患者中,辛伐他汀和 5-HT3 受体拮抗剂昂丹司琼联合使用的益处各不相同。我们在一项单独的试验中研究了它们各自的疗效和可能的协同作用,以改善精神分裂症的阴性症状。
这是一项为期 6 个月的随机、双盲、安慰剂对照试验,采用三中心、四臂、2×2 析因设计。共有 303 名年龄在 18-65 岁之间、病情稳定的精神分裂症患者被随机分配至加用昂丹司琼、辛伐他汀、两者或均不加用。主要结局是在 3 个月和 6 个月时阳性和阴性综合征量表(PANSS)的阴性评分。
混合模型分析和协方差分析显示,辛伐他汀或昂丹司琼均无主要作用,但两者之间存在显著的负交互作用( = 0.03);单独使用时,两种药物与安慰剂相比均能显著减轻阴性症状,但联合使用则无效。与安慰剂相比,辛伐他汀和昂丹司琼的个体治疗效果分别为-1.9 分(95%CI -3.23,-0.49; = 0.01)和-1.6 分(95%CI -3.00,-0.14; = 0.03)。联合治疗显著增加了抑郁和副作用。在治疗时间少于中位数 5 年的患者中,昂丹司琼改善了所有 PANSS 子量表、总体功能测量以及言语学习和流畅性,而辛伐他汀则没有。
辛伐他汀和昂丹司琼单独使用时对阴性症状的改善较小,联合使用时在治疗精神分裂症阴性症状方面没有协同作用。昂丹司琼在疾病发病 5 年内接受稳定抗精神病治疗的患者中表现出广泛的疗效。研究结果表明,昂丹司琼应该在有患精神病风险或早期治疗的患者中进行评估。