Su Kuan-Pin, Wu Po-Lun, Pariante Carmine M
Department of General Psychiatry, China Medical University Hospital, No. 2, Yuh-Der Road, Taichung 404, Taiwan.
Psychopharmacology (Berl). 2005 Dec;183(3):383-6. doi: 10.1007/s00213-005-0205-2. Epub 2005 Oct 21.
The results from case-control and retrospective studies revealed that olanzapine might be associated with more increased risks of metabolic dysfunction than risperidone. The crossover design can minimize the influence of individual variation in metabolic profiles and demographic variables, such as age, sex, concomitant medication use and personal life styles.
We design a crossover study to evaluate the metabolic effect of olanzapine and risperidone.
Fifteen schizophrenic patients were shifted from olanzapine and risperidone or from risperidone and olanzapine due to poor treatment response. The body weights, lipid profiles and fasting glucose levels were assessed before medication switch and 3 months after crossover.
In the seven patients taking risperidone at the time of inclusion (risperidone-first group), after shifting to olanzapine, there was a significant increase in triglyceride level (p=0.048) and body weight (p=0.008). In the other eight patients (olanzapine-first group), after shift to risperidone, there was a decrease in triglyceride level (p=0.009), body weight (p=0.049) and body mass index (BMI; p=0.04). When comparing the metabolic profiles in all patients after olanzapine and after risperidone (irrespective of the order of treatment), the mean triglyceride level (p=0.001), body weight (p=0.001) and BMI (p=0.015) were significantly higher in patients receiving olanzapine than in those receiving risperidone. Furthermore, there was a small increase in total cholesterol level (p=0.091) and a small decrease in high-density lipoprotein (HDL) level (p=0.061) in olanzapine group, but the differences did not reach a significant level. There was no significant difference between olanzapine and risperidone in fasting glucose and low-density lipoprotein (LDL).
This study confirms that elevated levels of triglyceride and body weight could be associated with the use of olanzapine as compared with risperidone. The changes in body weights and lipid profiles should be closely monitored in patients during treatment with atypical antipsychotic drugs.
病例对照研究和回顾性研究结果显示,与利培酮相比,奥氮平可能与更多的代谢功能障碍风险增加相关。交叉设计可以最大限度地减少个体代谢特征和人口统计学变量(如年龄、性别、合并用药情况和个人生活方式)差异的影响。
我们设计了一项交叉研究,以评估奥氮平和利培酮的代谢效应。
15名精神分裂症患者因治疗反应不佳,从奥氮平换用利培酮或从利培酮换用奥氮平。在换药前和交叉治疗3个月后评估体重、血脂谱和空腹血糖水平。
纳入时服用利培酮的7名患者(利培酮优先组),换用奥氮平后,甘油三酯水平(p = 0.048)和体重(p = 0.008)显著增加。在其他8名患者(奥氮平优先组)中,换用利培酮后,甘油三酯水平(p = 0.009)、体重(p = 0.049)和体重指数(BMI;p = 0.04)均下降。比较所有患者在服用奥氮平和利培酮后的代谢特征(无论治疗顺序如何),服用奥氮平的患者平均甘油三酯水平(p = 0.001)、体重(p = 0.001)和BMI(p = 0.015)显著高于服用利培酮的患者。此外,奥氮平组总胆固醇水平略有升高(p = 0.091),高密度脂蛋白(HDL)水平略有下降(p = 0.061),但差异未达到显著水平。奥氮平和利培酮在空腹血糖和低密度脂蛋白(LDL)方面无显著差异。
本研究证实,与利培酮相比,使用奥氮平可能与甘油三酯水平升高和体重增加有关。在非典型抗精神病药物治疗期间,应密切监测患者的体重和血脂谱变化。