Sheba Medical Center, Tel Hashomer 52621, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Sheba Medical Center, Tel Hashomer 52621, Israel.
Eur Neuropsychopharmacol. 2023 Aug;73:65-74. doi: 10.1016/j.euroneuro.2023.04.007. Epub 2023 Apr 30.
This large randomized controlled trial examined the effect of naproxen, simvastatin or both on patients with schizophrenia. This was a large multi-center, twelve-week, randomized, double-blind, placebo-controlled, four-arm clinical trial administering naproxen, simvastatin or both to 232 subjects with schizophrenia or schizoaffective disorder. The primary outcome was change in PANSS total score. ANCOVA and mixed model analyses of the PANSS total score change showed no significant difference between naproxen and placebo (adjusted p = 0.78), simvastatin and placebo (adjusted p = 0.38) or the combination of naproxen and simvastatin compared to placebo (adjusted p = 0.72). No statistically significant drug-placebo differences were found in the PANSS subscales, CGI or BACS between all groups. There was a near significant improvement in negative symptoms (p = 0.06), and an analysis of the 5 factor PANSS factors analysis found a significant improvement in simvastatin above placebo in withdrawal (p = 0.03). These finding were not significant after correcting for multiple comparisons. A meta-analysis on changes in total PANSS scores in studies on statins in schizophrenia, including the present study together with six other studies showed a significant improvement for statins compared to placebo (Hedges' G of -0.245 (CI= -0.403, -0.086, p = 0.002). When one outlying study which showed particularly strong effects of statins was removed, part of the effect went away. In conclusion, in this study, naproxen and simvastatin alone or in combination were not efficacious in the treatment of symptoms in schizophrenia. However, the meta-analysis of all studies of simvastatin for schizophrenia indicates further research on this topic.
这项大型随机对照试验研究了萘普生、辛伐他汀或两者联合治疗精神分裂症患者的效果。这是一项大型多中心、为期 12 周、随机、双盲、安慰剂对照、四臂临床试验,共纳入 232 例精神分裂症或分裂情感障碍患者,分别给予萘普生、辛伐他汀或两者联合治疗。主要结局是 PANSS 总分的变化。对 PANSS 总分变化的协方差分析和混合模型分析显示,萘普生与安慰剂(调整后 p=0.78)、辛伐他汀与安慰剂(调整后 p=0.38)或萘普生与辛伐他汀联合与安慰剂相比(调整后 p=0.72)无显著差异。在所有组之间,PANSS 分量表、CGI 或 BACS 均未发现药物与安慰剂之间存在统计学显著差异。阴性症状有显著改善(p=0.06),5 因子 PANSS 因子分析发现辛伐他汀的改善明显优于安慰剂(p=0.03)。在进行多次比较校正后,这些发现没有统计学意义。对包括本研究在内的 6 项他汀类药物治疗精神分裂症研究的 PANSS 总分变化进行荟萃分析显示,与安慰剂相比,他汀类药物有显著改善(Hedges' G 为-0.245(CI=-0.403,-0.086,p=0.002)。当去除一项显示他汀类药物作用特别强的异常研究后,部分效果消失。总之,在这项研究中,萘普生和辛伐他汀单独或联合治疗精神分裂症症状无效。然而,对所有辛伐他汀治疗精神分裂症的研究进行荟萃分析表明,需要进一步研究这一课题。