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首页> 外文期刊>Annals of General Psychiatry >Outcomes and safety of concomitant topiramate or metformin for antipsychotics-induced obesity: a randomized-controlled trial
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Outcomes and safety of concomitant topiramate or metformin for antipsychotics-induced obesity: a randomized-controlled trial

机译:伴随托吡酯或二甲双胍的结果和安全性用于抗精神病药诱导的肥胖症:随机对照试验

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Although there are some existing data describing the usage of topiramate in patients with antipsychotic-induced obesity, study on its comparison with metformin is limited. This study aimed to explore the effectiveness and safety of concomitant topiramate on antipsychotic-induced obesity as well as its comparison with metformin. 62 stabilized outpatients with antipsychotic-induced obesity were randomized into the topiramate group and the metformin group with 16-week treatment. The patients’ weight, body mass index (BMI), waist–hip ratio, and their side effects were assessed and compared. Intention-to-treat and completer analyses were performed. Meanwhile, covariance analysis was conducted to control the impact of the significant difference in BMI between the two groups. The two groups had comparable characteristics, though their difference in baseline BMI was significant. (1) Intention-to-treat analyses: the random missing values were replaced using the last observation carried forward method when intention-to-treat analyses were conducted. Compared with the baseline, the weight, BMI, and waist–hip ratio in the topiramate group markedly decreased at each follow-up, whereas, in the metformin group, only waist–hip ratio significantly decreased at 4 weeks after treatment. Compared with the metformin, only weight and BMI in the topiramate group were significantly decreased at week 4 after treatment, and at week 8–16, weight, BMI and waist–hip ratio were remarkably declined. (2) Completer analyses: compared with the baseline, the weight, BMI, and waist–hip ratio in the topiramate group at week 4–16 were markedly decreased, whereas only waist–hip ratio with metformin was significantly decreased at week 4. Compared with the metformin, all BMI with topiramate were markedly decreased at week 4–16. Moreover, its weight and waist–hip ratio also were notably lowered at week 8. No significant differences in adverse events were found between the two groups. Topiramate, similar to metformin in reducing obesity as previously reported, also significantly reduced body weight, BMI, and waist–hip ratio in patients with antipsychotic-induced obesity and demonstrated well tolerance in psychiatric patients. Trial registration The trial was registered at http://www.chictr.org.cn , and the number was ChiCTR-IPR-17013122.
机译:尽管存在一些现有的数据,但是描述了浸润性诱导肥胖患者托吡酯的使用,但与二甲双胍的比较有限的研究。本研究旨在探讨伴随托吡酯对抗精神病药诱导的肥胖症的有效性和安全性以及与二甲双胍的比较。将62稳定的抗精神病药诱导的肥胖的门诊患者随机分为16周的托氨酸基团和二甲双胍组。评估和比较患者体重,体重指数(BMI),腰臀比及其副作用。进行意向治疗和随访者分析。同时,进行协方差分析以控制两组之间BMI显着差异的影响。两组具有可比特征,尽管它们对基线BMI的差异很大。 (1)意图治疗分析:使用最后一次观察进行的随机观察进行了随机缺失值,当进行有意治疗分析时的前进方法。与基线相比,托特拉胺基团中的重量,BMI和腰臀比在每次随访中显着降低,而在二甲双胍组中,在治疗后4周只有腰臀比显着降低。与二甲双胍相比,在治疗后第4周只有在第4周,在第8-16期,重量,BMI和腰臀比例显着下降,只有重量和BMI显着降低。 (2)随意分析:与基线,第4-16周的托特拉胺组中的重量,BMI和腰臀比相比显着降低,而仅在第4周的腰部髋关节比二甲双胍的比例显着下降。比较用二甲双胍,在第4-16周的所有BMI中均具有显着降低。此外,其重量和腰臀比在第8周的情况下也显着降低。两组之间没有发现不良事件的显着差异。与先前报道的肥胖等肥胖相似的托吡酯,抗精神病药诱导肥胖症患者的体重,BMI和腰臀比例显着减少,并表现出精神病患者的耐受性。试用注册该试验在http://www.chictr.org.cn上注册,该数字是Chictr-IPR-17013122。

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