Department of Psychiatry, Vanderbilt University School of Medicine, Nashville, TN, USA.
Psychiatry Res. 2010 Apr 30;176(2-3):114-9. doi: 10.1016/j.psychres.2009.03.026. Epub 2010 Mar 2.
Melperone is an atypical antipsychotic drug that has been reported to be effective in treatment-resistant schizophrenia and L-DOPA psychosis. There are limited data concerning its effect on weight or body mass index (BMI). Weight and BMI were retrospectively compared in patients with schizophrenia treated with melperone (n=34), clozapine (n=225), or typical neuroleptics (n=74) for up to 3 months. Clozapine resulted in significant increases in weight and BMI from baseline to 6 weeks and 3 months. Neither melperone nor typical neuroleptics resulted in significant weight gain at either time point. Melperone did not result in significant increases in BMI. Weight and BMI were significantly lower with melperone compared with clozapine, but similar to typical neuroleptics. The proportion of melperone patients who experienced a >or=7% weight increase was lower than that in patients treated with clozapine and similar to that in patients treated with typical neuroleptics. Percent change in weight and BMI predicted improvement in BPRS total scores at 3 months in the clozapine group, but not in the melperone or typical neuroleptic groups. Because of the relationship between BMI and cardiovascular risk, melperone deserves further study as both a first line treatment and as an alternative to clozapine in refractory schizophrenia.
美哌隆是一种非典型抗精神病药物,据报道它对治疗抵抗性精神分裂症和 L-DOPA 精神病有效。关于它对体重或体重指数(BMI)的影响的数据有限。
我们回顾性比较了接受美哌隆(n=34)、氯氮平(n=225)或典型神经阻滞剂(n=74)治疗的精神分裂症患者的体重和 BMI,治疗时间最长达 3 个月。氯氮平治疗导致体重和 BMI 从基线到 6 周和 3 个月时显著增加。美哌隆和典型神经阻滞剂在任何时间点均未导致体重显著增加。美哌隆未导致 BMI 显著增加。与氯氮平相比,美哌隆组的体重和 BMI 显著较低,但与典型神经阻滞剂相似。与接受氯氮平治疗的患者相比,接受美哌隆治疗的患者体重增加>或=7%的比例较低,与接受典型神经阻滞剂治疗的患者相似。氯氮平组体重和 BMI 的百分比变化可预测 3 个月时 BPRS 总分的改善,但美哌隆组和典型神经阻滞剂组则无此预测作用。
由于 BMI 与心血管风险之间存在关联,因此美哌隆值得进一步研究,作为一线治疗药物,也可作为难治性精神分裂症患者的氯氮平替代药物。