Shao Ping, Ou Jianjun, Wu Renrong, Fang Maosheng, Chen Honghui, Xu Yi, Zhao Jingping
Department of Neurosis, Brain Hospital of Hunan Province, Changsha, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2013 Apr;38(4):365-9. doi: 10.3969/j.issn.1672-7347.2013.04.005.
To investigate the effect of ziprasidone and olanzapine on glucose and lipid metabolism in first-episode schizophrenia.
A total of 260 schizophrenics were assigned randomly to receive ziprasidone or olanzapine for 6 weeks. The weight was measured at baseline, week 2, 4 and 6. Fasting blood glucose (FBS), fasting insulin, high-density lipoprotein (HDL), total-cholesterol (TC) and triglycerides (TG) were measured at baseline and the end of 6-week treatment. Low-density lipoprotein (LDL) was measured in some patients at baseline and the end of 6-week treatment. Body mass index (BMI) and insulin resistance index (IRI) were counted.
A total of 245 patients completed the trial, including 121 ziprasidone patients and 124 olanzapine patients. The average dose was 137.5 mg/d for ziprasidone and 19.5 mg/d for olanzapine. Patients treated with olanzapine had higher weight gain than those treated with ziprasidone [(4.55±3.37) kg vs (-0.83±2.05) kg, P<0.001]. After the treatment, FBS, fasting insulin, HDL, TC, TG, LDL and IRI levels were significantly increased in the olanzapine group (all P values<0.001 ). However, in the ziprasidone group, FBS decreased significantly and HDL and TG levels increased significantly after the 6-week treatment (all P values<0.05). The mean changes of FBS, fasting insulin, TC, TG, LDL and IRI were significantly different in the two groups (all P values<0.001).
Ziprasidone has less glucose and lipid metabolic effect for first-episode schizophrenia patients in short-term treatment. However, olanzapine induces weight gain and dysfunction of glucose and lipid metabolism significantly, which is associated with increased risk of complications. When the doctors choose antipsychotics in the clinic, they should consider the side effects of the medication.
探讨齐拉西酮与奥氮平对首发精神分裂症患者糖脂代谢的影响。
将260例精神分裂症患者随机分为两组,分别接受齐拉西酮或奥氮平治疗6周。在基线、第2周、第4周和第6周测量体重。在基线和6周治疗结束时测量空腹血糖(FBS)、空腹胰岛素、高密度脂蛋白(HDL)、总胆固醇(TC)和甘油三酯(TG)。在部分患者的基线和6周治疗结束时测量低密度脂蛋白(LDL)。计算体重指数(BMI)和胰岛素抵抗指数(IRI)。
共有245例患者完成试验,其中齐拉西酮组121例,奥氮平组124例。齐拉西酮的平均剂量为137.5mg/d,奥氮平为19.5mg/d。奥氮平治疗的患者体重增加高于齐拉西酮治疗的患者[(4.55±3.37)kg对(-0.83±2.05)kg,P<0.001]。治疗后,奥氮平组的FBS、空腹胰岛素、HDL、TC、TG、LDL和IRI水平均显著升高(所有P值<0.001)。然而,在齐拉西酮组,6周治疗后FBS显著降低,HDL和TG水平显著升高(所有P值<0.05)。两组FBS、空腹胰岛素、TC、TG、LDL和IRI的平均变化有显著差异(所有P值<0.001)。
齐拉西酮对首发精神分裂症患者短期治疗的糖脂代谢影响较小。然而,奥氮平显著导致体重增加及糖脂代谢功能障碍,这与并发症风险增加有关。临床医生在选择抗精神病药物时,应考虑药物的副作用。