Perry Paul J, Argo Tami R, Carnahan Ryan M, Lund Brian C, Holman Timothy L, Ellingrod Vicki L, Miller Del
Department of Clinical and Administrative Pharmacy, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
J Clin Psychopharmacol. 2005 Jun;25(3):250-4. doi: 10.1097/01.jcp.0000162800.64378.82.
Atypical antipsychotics, including olanzapine, have been associated with clinically significant weight gain in some patients. The purpose of this study was to determine if weight gain was associated with increasing plasma concentrations during olanzapine treatment in subjects with schizophrenia. This study included 39 acutely ill subjects with schizophrenia, schizoaffective disorder, or schizophreniform disorder (DSM-III-R or DSM-IV). Assessments included the Brief Psychiatric Rating Scale (BPRS), the Scale for Assessment of Negative Symptoms (SANS), and weight measurements. Olanzapine was titrated to a dose of 5 to 20 mg/d for 2 to 6 weeks. A 24-hour plasma concentration was obtained after 6 weeks of treatment. Analysis using a receiver operator characteristic curve identified a threshold dose-weighted plasma concentration of 20.6 ng/mL being associated with an increased likelihood of clinically significant weight gain (> or =7% baseline weight) during olanzapine treatment. The associations remained significant after adjusting for age, gender, baseline body mass index, baseline symptom severity, and symptom improvement (OR = 10.1; 95% CI, 1.3-75.0; P = 0.024). Similar analysis determined that a threshold olanzapine dose of 13.3 mg/d was associated with > or =7% weight gain. However, after adjusting for potential confounders, the results did not remain significant. The association of weight gain with plasma concentrations during treatment with olanzapine may support the utilization of plasma drug concentration as a marker for antipsychotic-induced weight gain in the treatment of schizophrenia.
包括奥氮平在内的非典型抗精神病药物,在一些患者中与临床上显著的体重增加有关。本研究的目的是确定在精神分裂症患者的奥氮平治疗期间,体重增加是否与血浆浓度升高有关。本研究纳入了39名患有精神分裂症、分裂情感性障碍或精神分裂症样障碍(DSM-III-R或DSM-IV)的急性病患者。评估包括简明精神病评定量表(BPRS)、阴性症状评定量表(SANS)和体重测量。奥氮平滴定至5至20mg/d的剂量,持续2至6周。治疗6周后获取24小时血浆浓度。使用受试者工作特征曲线进行分析,确定阈值剂量加权血浆浓度为20.6ng/mL与奥氮平治疗期间临床上显著体重增加(≥基线体重的7%)的可能性增加相关。在对年龄、性别、基线体重指数、基线症状严重程度和症状改善进行校正后,这种相关性仍然显著(OR = 10.1;95%CI,1.3 - 75.0;P = 0.024)。类似分析确定奥氮平阈值剂量为13.3mg/d与≥7%的体重增加相关。然而,在对潜在混杂因素进行校正后,结果不再显著。奥氮平治疗期间体重增加与血浆浓度之间的关联可能支持将血浆药物浓度用作精神分裂症治疗中抗精神病药物所致体重增加的标志物。