Vieta Eduard, Durgam Suresh, Lu Kaifeng, Ruth Adam, Debelle Marc, Zukin Stephen
Bipolar Disorder Unit, Institute of Neuroscience, Hospital Clinic, University of Barcelona, IDIBAPS, CIBERSAM, Barcelona, Catalonia, Spain.
Forest Research Institute, Jersey City, NJ, USA.
Eur Neuropsychopharmacol. 2015 Nov;25(11):1882-91. doi: 10.1016/j.euroneuro.2015.08.020. Epub 2015 Sep 5.
Bipolar I disorder is a chronic disorder characterized by episodic recurrences of mania, depression, and mixed affective states interspersed with periods of full or partial remission; subsyndromal residual symptoms between episodes are common and disabling. Cariprazine, an atypical antipsychotic, is a potent dopamine D3 and D2 receptor partial agonist with preferential binding to D3 receptors. Post-hoc analyses of pooled data from 3 positive trials were conducted to evaluate the effect of cariprazine 3-12 mg/d on the symptoms of mania in inpatients (18-65 years) with bipolar I disorder and a current manic episode. Analyses were based on the pooled intent-to-treat (ITT) population (placebo=429; cariprazine=608). Mean change from baseline to the end of treatment on individual Young Mania Rating Scale (YMRS) items was analysed using a mixed-effects model for repeated measures (MMRM); categorical symptom severity shifts were analysed using logistic regression. Statistically significant improvement in mean change was seen for cariprazine versus placebo on all 11 YMRS items (p<0.0001); significantly more cariprazine- versus placebo-treated patients had mild/no symptoms at the end of treatment on 11 YMRS items (p<0.0001) and concurrently on the 4 YMRS core symptoms (irritability, speech, content, and disruptive-aggressive behaviour) (p<0.0001). Significantly more cariprazine- versus placebo-treated patients shifted from a Moderate/Worse or Marked/Worse Symptoms categories to Mild/No Symptoms on all 11 (p<0.0001) and 9 of 11 YMRS items (p<0.05), respectively. Results suggest that cariprazine treatment improved mania across YMRS symptoms; a significant percentage of cariprazine- versus placebo-treated patients had mild/no symptoms at the end of treatment.
双相 I 型障碍是一种慢性疾病,其特征为躁狂、抑郁和混合情感状态的发作性复发,期间穿插着完全或部分缓解期;发作之间的亚综合征残留症状很常见且会导致功能障碍。卡立普嗪是一种非典型抗精神病药物,是一种强效的多巴胺 D3 和 D2 受体部分激动剂,对 D3 受体具有优先结合作用。对 3 项阳性试验的汇总数据进行事后分析,以评估卡立普嗪 3 - 12 mg/d 对患有双相 I 型障碍且当前处于躁狂发作的住院患者(18 - 65 岁)躁狂症状的影响。分析基于汇总的意向性治疗(ITT)人群(安慰剂组 = 429 例;卡立普嗪组 = 608 例)。使用重复测量的混合效应模型(MMRM)分析从基线到治疗结束时个体杨氏躁狂评定量表(YMRS)项目的平均变化;使用逻辑回归分析分类症状严重程度的变化。在所有 11 个 YMRS 项目上,卡立普嗪组与安慰剂组相比,平均变化有统计学显著改善(p < 0.0001);在治疗结束时,接受卡立普嗪治疗的患者在 11 个 YMRS 项目上出现轻度/无症状的比例显著高于安慰剂组(p < 0.0001),同时在 4 个 YMRS 核心症状(易怒、言语、内容和破坏 - 攻击行为)上也是如此(p < 0.0001)。接受卡立普嗪治疗的患者与接受安慰剂治疗的患者相比,在所有 11 个(p < 0.0001)和 11 个 YMRS 项目中的 9 个(p < 0.05)上,从“中度/更严重”或“显著/更严重”症状类别转变为“轻度/无”症状的比例显著更高。结果表明,卡立普嗪治疗可改善 YMRS 症状方面的躁狂;与接受安慰剂治疗的患者相比,接受卡立普嗪治疗的患者中有相当比例在治疗结束时出现轻度/无症状。