Biological Psychiatry Division, Medical University Innsbruck, Innsbruck, Austria.
Int J Neuropsychopharmacol. 2010 Sep;13(8):1115-25. doi: 10.1017/S1461145710000490. Epub 2010 May 12.
Clozapine is associated with significant weight gain and metabolic disturbances. This multicentre, randomized study comprised a double-blind, placebo-controlled treatment phase of 16 wk, and an open-label extension phase of 12 wk. Outpatients who met DSM-IV-TR criteria for schizophrenia, who were not optimally controlled while on stable dosage of clozapine for > or =3 months and had experienced weight gain of > or =2.5 kg while taking clozapine, were randomized (n=207) to aripiprazole at 5-15 mg/d or placebo, in addition to a stable dose of clozapine. The primary endpoint was mean change from baseline in body weight at week 16 (last observation carried forward). Secondary endpoints included clinical efficacy, body mass index (BMI) and waist circumference. A statistically significant difference in weight loss was reported for aripiprazole vs. placebo (-2.53 kg vs. -0.38 kg, respectively, difference=-2.15 kg, p<0.001). Aripiprazole-treated patients also showed BMI (median reduction 0.8 kg/m(2)) and waist circumference reduction (median reduction 2.0 cm) vs. placebo (no change in either parameter, p<0.001 and p=0.001, respectively). Aripiprazole-treated patients had significantly greater reductions in total and low-density lipoprotein (LDL) cholesterol. There were no significant differences in Positive and Negative Syndrome Scale total score changes between groups but Clinical Global Impression Improvement and Investigator's Assessment Questionnaire scores favoured aripiprazole over placebo. Safety and tolerability were generally comparable between groups. Combining aripiprazole and clozapine resulted in significant weight, BMI and fasting cholesterol benefits to patients suboptimally treated with clozapine. Improvements may reduce metabolic risk factors associated with clozapine treatment.
氯氮平会引起明显的体重增加和代谢紊乱。这项多中心、随机研究包括 16 周的双盲、安慰剂对照治疗期和 12 周的开放标签扩展期。符合 DSM-IV-TR 精神分裂症标准、在服用氯氮平稳定剂量>或=3 个月时未得到最佳控制且在服用氯氮平时体重增加>或=2.5kg 的门诊患者,随机(n=207)接受阿立哌唑 5-15mg/d 或安慰剂,同时服用氯氮平稳定剂量。主要终点是第 16 周(末次观察结转)时体重相对于基线的平均变化。次要终点包括临床疗效、体重指数(BMI)和腰围。阿立哌唑与安慰剂相比,体重减轻有统计学意义(分别为-2.53kg 和-0.38kg,差异=-2.15kg,p<0.001)。与安慰剂相比,阿立哌唑治疗的患者还显示出 BMI(中位数降低 0.8kg/m2)和腰围减少(中位数降低 2.0cm)(两个参数均无变化,p<0.001 和 p=0.001)。阿立哌唑治疗的患者总胆固醇和低密度脂蛋白(LDL)胆固醇降低更为显著。两组间阳性和阴性综合征量表总分变化无显著差异,但临床总体印象改善和研究者评估问卷评分均显示阿立哌唑优于安慰剂。安全性和耐受性在一般情况下两组间无显著差异。阿立哌唑联合氯氮平可使氯氮平治疗效果不理想的患者体重、BMI 和空腹胆固醇显著获益。这些改善可能会降低与氯氮平治疗相关的代谢危险因素。