Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD 21228, USA.
J Clin Psychopharmacol. 2011 Feb;31(1):86-91. doi: 10.1097/JCP.0b013e318204825b.
Weight gain is a major adverse effect of several second-generation antipsychotic medications. Rimonabant is a cannabinoid-1 receptor antagonist that promotes weight loss in the general population. We conducted a 16-week, double-blind, placebo-controlled study of rimonabant (20 mg/d) in people with schizophrenia or schizoaffective disorder, based on the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria, who were clinically stable on second-generation antipsychotics. Participants had a body mass index of 27 kg/m or higher with hyperlipidemia or body mass index of 30 kg/m or higher, and no current substance abuse/dependence (except nicotine), more than weekly cannabis use, or recent depressive symptoms/suicidality. An exercise and dietary counseling group was offered weekly. Target enrollment was 60; the trial was terminated early because of withdrawal of rimonabant from the European market. Fifteen participants were randomized (7 rimonabant, 8 placebo); 5 completed in each group. Rimonabant was associated with a greater reduction in Brief Psychiatric Rating Scale total score versus placebo (mean ± SE difference, -1.9 ± 0.8, P = 0.02), driven by differences in the Brief Psychiatric Rating Scale anxiety/depression (-1.4 ± 0.35, P = 0.0004) and hostility (-0.7 ± 0.3, P = 0.02) factors. Group differences were not significant for the Calgary Depression Scale total score (P = 0.24), Scale for the Assessment of Negative Symptoms total score (P = 0.13), weight, blood pressure, or fasting lipids or glucose. Rimonabant was well tolerated with no significant adverse events. No significant weight loss, metabolic effects, or adverse psychiatric effects were associated with the cannabinoid-1 receptor antagonist rimonabant in this small sample of people with schizophrenia. The endocannabinoid system remains a promising target for pharmacotherapy of schizophrenia and obesity.
体重增加是几种第二代抗精神病药物的主要不良反应。利莫那班是一种大麻素 1 型受体拮抗剂,可促进普通人群体重下降。我们根据《精神障碍诊断与统计手册》第四版标准,对接受第二代抗精神病药物治疗且病情稳定的精神分裂症或分裂情感性障碍患者进行了一项为期 16 周、双盲、安慰剂对照的利莫那班(20mg/d)研究。参与者的体重指数(BMI)为 27kg/m2 或更高,伴血脂异常,或 BMI 为 30kg/m2 或更高,且无当前物质滥用/依赖(尼古丁除外)、每周使用大麻超过一次、近期抑郁症状/自杀意念。每周提供一次运动和饮食咨询。目标入组人数为 60 人;由于利莫那班撤出欧洲市场,试验提前终止。15 名参与者被随机分配(利莫那班 7 人,安慰剂 8 人);每组各有 5 人完成。与安慰剂相比,利莫那班治疗组简明精神病评定量表总分下降更为显著(平均 ± SE 差值,-1.9 ± 0.8,P = 0.02),这主要归因于简明精神病评定量表焦虑/抑郁因子(-1.4 ± 0.35,P = 0.0004)和敌意因子(-0.7 ± 0.3,P = 0.02)的差异。两组间在 Calgary 抑郁量表总分(P = 0.24)、阴性症状评定量表总分(P = 0.13)、体重、血压、空腹血脂或血糖方面无显著差异。利莫那班耐受性良好,无显著不良事件。在这项小样本精神分裂症患者研究中,大麻素 1 型受体拮抗剂利莫那班未导致显著体重减轻、代谢效应或不良精神效应。内源性大麻素系统仍然是精神分裂症和肥胖症药物治疗的一个有前途的靶点。