Metabolic effects of Olanzapine versus Iloperidone: A 24 weeks randomized, prospective, interventional study

Shivangna Singh, Shalini Chandra, A. Kapoor, H. K. Singh, R. Kant
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引用次数: 1

Abstract

Atypical antipsychotics have become the mainstay of therapy for psychosis. Though extrapyramidal side effects have been reduced with atypical antipsychotics, yet there are increased concerns over metabolic effects. The present study is aimed to comparatively evaluate the metabolic profile of olanzapine and iloperidone in cases of psychosis. A prospective, randomized, open label, observational study of 6 months duration was conducted in the Department of Pharmacology and Department of Psychiatry, Rohilkhand Medical College and Hospital, Bareilly. A total of 62 patients of both sexes newly diagnosed with psychosis (ICD-10, F20- F29) were included in the study, 31 each in olanzapine and iloperidone groups. Demographic parameters were recorded, following which the patient’s body weight, BMI, fasting blood sugar and lipid profile were estimated at baseline. Follow-up of the patients was done periodically after one month, three months and six months. Olanzapine treated patients showed markedly significant rise in body weight up to 7 kg at the endpoint (p<0.0001) at each follow-up, with a significant increase in BMI. Rise in fasting blood sugar (FBS), total cholesterol (TC), triglycerides (TG) and low-density lipoprotein (LDL) levels werealso statistically significant. At the same time, significant decrease in HDL levels was also observed. Iloperidone treated patients showed statistically significant less rise in body weight (upto 1kg, p<0.05) and BMI. No significant changes in fasting blood sugar, total cholesterol, LDL and HDL levels were noted, while TG levels were significantly reduced. Iloperidone caused numerically less rise in bodyweight and BMI, and fewer metabolic adverse effects as compared to olanzapine, and hence should be preferred. Keywords: Atypical antipsychotics; Weight gain; Blood sugar level; Dyslipidemia
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奥氮平与依哌啶酮的代谢影响:一项为期24周的随机、前瞻性、干预性研究
非典型抗精神病药物已成为治疗精神病的主要药物。虽然非典型抗精神病药物的锥体外系副作用已经减少,但对代谢影响的担忧却在增加。本研究旨在比较评价奥氮平和依哌啶酮在精神病患者中的代谢特征。在barilly Rohilkhand医学院和医院药理学和精神病学学系进行了一项为期6个月的前瞻性、随机、开放标签的观察性研究。本研究共纳入62例新诊断为精神病(ICD-10, F20- F29)的男女患者,其中奥氮平组和伊operidone组各31例。记录人口统计学参数,然后在基线时估计患者的体重、BMI、空腹血糖和血脂。随访时间分别为1个月、3个月和6个月。在每次随访中,奥氮平治疗的患者在终点体重显著增加至7 kg (p<0.0001), BMI显著增加。空腹血糖(FBS)、总胆固醇(TC)、甘油三酯(TG)和低密度脂蛋白(LDL)水平的升高也具有统计学意义。同时,高密度脂蛋白水平也显著降低。依哌啶酮组患者体重(最高达1kg, p<0.05)和BMI升高幅度均有统计学意义。空腹血糖、总胆固醇、低密度脂蛋白和高密度脂蛋白水平无明显变化,而TG水平明显降低。与奥氮平相比,伊operidone引起的体重和BMI数值上升更小,代谢不良反应更少,因此应首选。关键词:非典型抗精神病药物;体重增加;血糖水平;血脂异常
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