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Zonisamide for weight loss in obese adults: a randomized controlled trial.

机译:唑尼沙胺对肥胖成年人的体重减轻:一项随机对照试验。

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CONTEXT: Zonisamide is a marketed antiepileptic drug that has serotonergic and dopaminergic activity in addition to blockade of sodium and calcium channels. Weight loss was an adverse effect associated with zonisamide treatment in epilepsy clinical trials. OBJECTIVE: To evaluate the efficacy of zonisamide for weight loss in obese adults. DESIGN AND SETTING: Sixteen-week randomized, double-blind, placebo-controlled trial with an optional single-blind extension of the same treatment for another 16 weeks, conducted at Duke University Medical Center from March 2001 to March 2002. PARTICIPANTS: Fifty-five (92%) women and 5 (8%) men (mean [SE] body mass index, 36.3 [0.5]; mean age, 37.0 (1.0) years). INTERVENTIONS: Patients were randomly assigned to receive zonisamide (n = 30) or placebo (n = 30). All participants were prescribed a balanced hypocaloric diet (500 kcal/d deficit) and compliance was monitored with self-rated food diaries. Zonisamide therapy was started at 100 mg/d orally, with gradual increase to 400 mg/d and further increase to 600 mg/d for patients losing less than 5% of body weight at the end of 12 weeks. Placebo dosing was identical. MAIN OUTCOME MEASURE: Change in body weight. RESULTS: Of the 60 randomized patients, 51 completed the 16-week acute phase. In an intent-to-treat analysis using the available data for all randomized participants with the last observation carried forward, the zonisamide group lost more body weight than the placebo group (mean [SE], 5.9 [0.8] kg [6.0% loss] vs 0.9 [0.4] kg [1.0% loss]; t = 5.5; P<.001) during the 16-week period. A longitudinal mixed-model regression for weight change controlling for age, race, sex, body mass index, and percent body fat estimated that zonisamide treatment over the 16-week study duration was associated with significantly greater weight loss than was placebo (t = 6.4; P<.001). Seventeen (57%) of 30 in the zonisamide group and 3 (10%) of 30 in the placebo group lost at least 5% of body weight (P<.001) by week 16. Of the 37 participants who entered the extension phase, 36 completed week 32. The zonisamide group (n = 19) had a mean weight loss of 9.2 kg (1.7 kg) (9.4% loss) at week 32 compared with 1.5 kg (0.7 kg) (1.8% loss) for the placebo group (n = 17) (t = 4.0; P<.001). Zonisamide was tolerated well, with few adverse effects. CONCLUSION: In this short-term, preliminary trial, zonisamide and hypocaloric diet resulted in more weight loss than placebo and hypocaloric diet in the treatment of obesity.
机译:背景:唑尼沙胺是一种市售的抗癫痫药,除了阻断钠和钙通道外,还具有血清素和多巴胺能活性。在癫痫临床试验中,体重减轻是与唑尼沙胺治疗相关的不良反应。目的:评估唑尼沙胺对肥胖成人体重减轻的疗效。设计与背景:2001年3月至2002年3月在杜克大学医学中心进行的为期16周的随机,双盲,安慰剂对照试验,可选地将同一治疗单盲延长了另外16周。参与者:五十名5名女性(92%)和5名男性(8%)(平均[SE]体重指数为36.3 [0.5];平均年龄为37.0(1.0)岁)。干预措施:患者被随机分配接受唑尼沙胺(n = 30)或安慰剂(n = 30)。所有参与者都被要求均衡的低热量饮食(500 kcal / d的赤字),并通过自我评估的食物日记来监测依从性。唑尼沙胺治疗从口服开始以100 mg / d开始,逐渐增加至400 mg / d,并在12周末体重减轻少于5%的患者逐渐增加至600 mg / d。安慰剂的剂量是相同的。主要观察指标:体重改变。结果:在随机分组的60例患者中,有51例完成了16周的急性期。在一项意向性治疗分析中,使用所有随机参与者的可用数据并进行了最后观察,结果发现,唑尼沙胺组的体重较安慰剂组减轻了更多(平均[SE],5.9 [0.8] kg [6.0%降低]与16周内的0.9 [0.4] kg [损失1.0%]; t = 5.5; P <.001)。通过控制年龄,种族,性别,体重指数和体脂百分比的体重变化的纵向混合模型回归估计,在16周的研究期间,唑尼沙胺治疗的体重减轻明显大于安慰剂(t = 6.4) ; P <.001)。到第16周时,zonisamide组的30名中的十七名(57%)和安慰剂组中的30名中的3名(10%)在第16周时体重减轻了至少5%(P <.001)。 ,在第32周完成了36次。zonisamide组(n = 19)在第32周的平均体重减轻了9.2 kg(1.7 kg)(降低了9.4%),而安慰剂组的平均体重减轻了1.5 kg(0.7 kg)(降低了1.8%)。组(n = 17)(t = 4.0; P <.001)。唑尼沙胺耐受良好,几乎没有不良反应。结论:在这项短期的初步试验中,zonisamide和低热量饮食在肥胖症治疗中的体重减轻比安慰剂和低热量饮食多。

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