Citrome Leslie, Álvarez-Barón Elena, Gabarda-Inat Irene, Thangavelu Karthinathan, Tocco Michael
Department of Psychiatry and Behavioral Sciences, New York Medical College, Valhalla, New York, USA.
Angelini Pharma S.p.a, Global Medical Department, Rome, Italy.
Int Clin Psychopharmacol. 2025 Jul 1;40(4):214-223. doi: 10.1097/YIC.0000000000000563. Epub 2024 Jul 22.
Symptoms of hostility in patients during acute exacerbations of schizophrenia have been associated with aggressive behavior. Data suggest that some second-generation antipsychotics have specific anti-hostility effects, independent of sedation and positive symptom improvement. Two post hoc analyses were performed to examine the efficacy of lurasidone for reducing hostility in patients with schizophrenia. One analysis pooled adults ( N = 1168) from 5 placebo-controlled, 6-week trials of lurasidone (40-160 mg). Another analysis pooled younger patients (up to age 25 years, N = 427) from the adult studies and a similarly designed trial of lurasidone (40 or 80 mg) in adolescent patients (13-17 years old). The outcome measure was mean change in the hostility item (P7) of the Positive and Negative Syndrome Scale (PANSS). To address pseudospecificity, results were adjusted for positive symptom change and sedation. In adults with a baseline PANSS hostility score ≥2, significant improvement in hostility was observed for all doses with a dose-related increase in effect size (Cohen's d): lurasidone 40 mg = 0.18, 80 mg = 0.24, 120 mg = 0.36, and 160 mg = 0.53. The same dose-response pattern was observed for the more severe hostility subgroups (P7: ≥3, ≥4), and in the early-onset population. Results suggest that lurasidone has specific, dose-related anti-hostility effects.
精神分裂症急性加重期患者的敌意症状与攻击行为有关。数据表明,一些第二代抗精神病药物具有特定的抗敌意作用,独立于镇静作用和阳性症状的改善。进行了两项事后分析,以检验鲁拉西酮对降低精神分裂症患者敌意的疗效。一项分析汇总了来自5项鲁拉西酮(40 - 160毫克)安慰剂对照、为期6周试验的成人(N = 1168)。另一项分析汇总了来自成人研究的年轻患者(年龄最大25岁,N = 427)以及一项针对青少年患者(13 - 17岁)设计类似的鲁拉西酮(40或80毫克)试验。结局指标是阳性和阴性症状量表(PANSS)中敌意项目(P7)的平均变化。为解决伪特异性问题,对结果进行了阳性症状变化和镇静的校正。在基线PANSS敌意评分≥2的成人中,所有剂量的敌意均有显著改善,且效应量呈剂量相关增加(科恩d值):鲁拉西酮40毫克 = 0.18,80毫克 = 0.24,120毫克 = 0.36,160毫克 = 0.53。在更严重的敌意亚组(P7:≥3,≥4)以及早发人群中也观察到了相同的剂量反应模式。结果表明,鲁拉西酮具有特定的、剂量相关的抗敌意作用。