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A naturalistic comparison of the long-term metabolic adverse effects of clozapine versus other antipsychotics for patients with psychotic illnesses

机译:氯氮平与其他抗精神病药对精神病患者长期代谢不良反应的自然比较

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OBJECTIVE: Clozapine, an evidence-based treatment of refractory schizophrenia, is associated with increased weight gain and metabolic dysregulation compared with most antipsychotics in short-term clinical trials. However, there are limited data describing comparative long-term metabolic risks. In this report, we examined whether short-term differences persist with long-term exposure to clozapine. METHODS: The data of all patients in a university-based clinic with a psychotic illness or a mood disorder with psychotic features, based on the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision diagnosis, and treated with an antipsychotic in calendar year 2012 were examined. A total of 307 patients met the criteria; 96 patients were treated with clozapine and the remaining 211 patients were treated with 1 or more non-clozapine antipsychotics. Body mass index, type 2 diabetes, hypertension, dyslipidemia, and obesity were compared. RESULTS: The mean duration of the clozapine treatment was 7.6 years (range, 2 months to 21 y). On all metabolic measures, there were no statistically significant differences between the clozapine and non-clozapine groups (mean body mass index, 31 vs 32; type 2 diabetes, 17% vs 18%; dyslipidemia, 35% vs 38%; hypertension, 32% vs 39%; and obesity, 48% vs 54%). Removing the olanzapine-treated patients (n = 51) from the non-clozapine group did not change the findings. CONCLUSIONS: In this university-based clinic sample with a large number of clozapine-treated patients, we found no evidence of increased risk in any individual measure for those receiving clozapine. Although speculative, the relative contribution of the increased short-term metabolic risk associated with clozapine may be diminished over time because multiple other variables likely also impact metabolic risk during the life span. Although speculative, the relative contribution of the increased short-term metabolic risk associated with clozapine may be diminished over time due to the accumulated impact of other variables that also impact metabolic risk across the life span.
机译:目的:在短期临床试验中,与大多数抗精神病药相比,氯氮平是一种基于证据的难治性精神分裂症治疗,与体重增加和代谢异常相关。但是,描述相对长期代谢风险的数据有限。在本报告中,我们研究了长期接触氯氮平后短期持续存在差异。方法:根据《精神疾病诊断和统计手册》第四版,文本修订版诊断,并在日历中接受抗精神病药物治疗,以大学为基础的诊所中患有精神病或具有精神病特征的情绪障碍的所有患者的数据2012年进行了检查。共有307名患者符合标准。 96例患者接受了氯氮平治疗,其余211例患者接受了1种或多种非氯氮平抗精神病药治疗。比较了体重指数,2型糖尿病,高血压,血脂异常和肥胖症。结果:氯氮平治疗的平均持续时间为7.6年(范围2个月至21年)。在所有代谢指标上,氯氮平组和非氯氮平组之间均无统计学差异(平均体重指数分别为31 vs 32; 2型糖尿病,分别为17%vs 18%;血脂异常,35%vs 38%;高血压,32 %vs 39%;肥胖症48%vs 54%)。从非氯氮平组中删除奥氮平治疗的患者(n = 51)不会改变结果。结论:在这个基于大学的临床样本中,有大量接受氯氮平治疗的患者,我们没有发现任何证据表明接受氯氮平治疗的患者的任何单独措施均会增加风险。尽管是推测性的,但随着时间的流逝,与氯氮平相关的短期代谢风险增加的相对贡献可能会降低,因为多个其他变量也可能影响生命周期中的代谢风险。尽管是推测性的,但由于其他变量的累积影响也会影响整个寿命期间的代谢风险,因此与氯氮平相关的短期代谢风险增加的相对贡献可能会随着时间的推移而减少。

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