Department of Psychiatry, National Clinical Research Center for Mental Disorders, and National Center for Mental Disorders, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, China.
Department of Psychiatry, First Affiliated Hospital of Kunming Medical University, Kunming 650032, Yunnan, China.
Int J Neuropsychopharmacol. 2024 Nov 1;27(11). doi: 10.1093/ijnp/pyae052.
This study aimed to evaluate the efficacy and safety of lumateperone in treating bipolar disorder and schizophrenia. A comprehensive literature search was conducted across multiple databases and websites from inception to July 16, 2024, to identify both published and unpublished randomized controlled trials (RCTs). Meta-analyses were performed using random-effects or fixed-effects models depending on statistical heterogeneity. Relative risks (RRs) or standardized mean differences (SMDs) with 95% confidence intervals (CIs) were used to summarize the effects. Out of 931 records screened, 7 RCTs (four focusing on bipolar depression and 3 on schizophrenia) were eligible for inclusion. Lumateperone was efficacious in reducing depressive symptoms in bipolar depression (SMDs = -0.36, 95% CI: -.59 to -.13). In treating schizophrenia, lumateperone exhibited a lower combined SMD of -0.14 (95% CI: -.27 to 0, P = .051, I² = 49.6%), showing no significant difference from the placebo group, although the P-value approached significance. The lumateperone group showed significantly higher response rates compared with placebo in both bipolar depression (RRs = 1.27, 95% CI = 1.07 to 1.51) and schizophrenia (RRs = 1.44, 95% CI = 1.12 to 1.86). Common treatment-emergent adverse events included somnolence, dry mouth, dizziness, nausea, and headache (RRs = 1.30 to 3.29). Importantly, lumateperone did not significantly increase extrapyramidal symptoms (EPS, RRs = 1.46, 95% CI = .84 to 2.53). Lumateperone is effective in treating bipolar depression but does not significantly reduce symptom severity in schizophrenia. It has a favorable safety and tolerability profile. However, caution is warranted in interpreting these findings due to the limited number of studies included.
这项研究旨在评估卢美哌隆治疗双相情感障碍和精神分裂症的疗效和安全性。我们对多个数据库和网站进行了全面的文献检索,检索时间从建库至 2024 年 7 月 16 日,以确定已发表和未发表的随机对照试验(RCT)。Meta 分析采用随机效应或固定效应模型,具体取决于统计学异质性。相对风险(RR)或标准化均数差(SMD)及其 95%置信区间(CI)用于总结效应。在筛选出的 931 条记录中,有 7 项 RCT(4 项聚焦于双相抑郁,3 项聚焦于精神分裂症)符合纳入标准。卢美哌隆在治疗双相抑郁时能有效减轻抑郁症状(SMD = -0.36,95%CI:-0.59 至 -0.13)。在治疗精神分裂症时,卢美哌隆的联合 SMD 为 -0.14(95%CI:-0.27 至 0,P =.051,I² = 49.6%),与安慰剂组无显著差异,尽管 P 值接近显著水平。在双相抑郁和精神分裂症中,与安慰剂组相比,卢美哌隆组的应答率均显著升高(双相抑郁:RRs = 1.27,95%CI = 1.07 至 1.51;精神分裂症:RRs = 1.44,95%CI = 1.12 至 1.86)。常见的治疗中出现的不良事件包括嗜睡、口干、头晕、恶心和头痛(RRs = 1.30 至 3.29)。重要的是,卢美哌隆并未显著增加锥体外系症状(EPS,RRs = 1.46,95%CI =.84 至 2.53)。卢美哌隆治疗双相抑郁有效,但对精神分裂症的症状严重程度无显著改善。它具有良好的安全性和耐受性。然而,由于纳入的研究数量有限,在解释这些发现时需要谨慎。