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Comparison of metabolic effects of ziprasidone versus olanzapine treatment in patients with first-episode schizophrenia

机译:齐拉西酮与奥氮平治疗首发精神分裂症患者的代谢作用比较

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Objective: The objective of the study was to compare metabolic effects of ziprasidone versus olanzapine treatment in patients with first-episode schizophrenia. Methods: In this 6-week, multicenter, open-label trial, 260 patients were randomly assigned to receive ziprasidone or olanzapine treatment (130 per group). Primary metabolic measures were changes in weight and body mass index (BMI). Secondary metabolic measures were changes in glucose, insulin, lipids, and blood pressure. Efficacy and safety were also measured additionally. Results: A total number of 230 patients completed the study. The mean daily dosages were 138.2(28.6) mg for ziprasidone and 19.0(2.3) mg for olanzapine. After 6-week treatment, there were significant between-group differences in change scores on weight [4.22(3.49) kg versus -0.84(2.04) kg, p < 0.001] and BMI [1.59(1.37) versus -0.30(0.74), p < 0.001]. In addition, there were significant between-group differences in change scores on fasting plasma glucose, insulin, homeostasis model assessment 2-insulin resistance, low-density lipoprotein, total cholesterol, and triglycerides (p < 0.001); all the changes were clinically in favor of ziprasidone treatment. Both medications were effective in improving schizophrenia symptoms, but the decreases in Positive and Negative Syndrome Scale total scores of the olanzapine group were significantly greater than that of the ziprasidone group (p < 0.05). Compared with olanzapine, ziprasidone also induced more prolonging of corrected QT interval and extrapyramidal side effects (p < 0.05). Both medications were well tolerated, and no serious adverse events were observed in either group. Conclusions: Compared with olanzapine, ziprasidone treatment was associated with less adverse effects on glucose and lipid metabolism in patients with first-episode schizophrenia.
机译:目的:本研究的目的是比较齐拉西酮和奥氮平对首发精神分裂症患者的代谢作用。方法:在为期6周的多中心开放标签试验中,随机分配260名患者接受齐拉西酮或奥氮平治疗(每组130名)。主要的代谢指标是体重和体重指数(BMI)的变化。次要的代谢指标是葡萄糖,胰岛素,脂质和血压的变化。功效和安全性也被另外测量。结果:总共230位患者完成了研究。齐拉西酮的平均日剂量为138.2(28.6)mg,奥氮平为19.0(2.3)mg。经过6周的治疗,体重变化评分的组间差异显着[4.22(3.49)kg对-0.84(2.04)kg,p <0.001]和BMI [1.59(1.37)对-0.30(0.74), p <0.001]。此外,空腹血糖,胰岛素,体内稳态模型评估2-胰岛素抵抗,低密度脂蛋白,总胆固醇和甘油三酸酯的变化评分之间存在显着的组间差异(p <0.001);所有这些变化在临床上均支持齐拉西酮治疗。两种药物均可有效改善精神分裂症症状,但奥氮平组的阳性和阴性综合征量表总分的降低明显大于齐拉西酮组(p <0.05)。与奥氮平相比,齐拉西酮还引起更正的QT间期延长和锥体束外副作用(p <0.05)。两种药物的耐受性良好,两组均未观察到严重不良事件。结论:与奥氮平相比,齐拉西酮治疗对首发精神分裂症患者的葡萄糖和脂质代谢的不良影响较小。

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