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首页> 外文期刊>Sleep >A randomized, double-blind, placebo-controlled study of an oral, extended-release formulation of phentermine/topiramate for the treatment of obstructive sleep apnea in obese adults
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A randomized, double-blind, placebo-controlled study of an oral, extended-release formulation of phentermine/topiramate for the treatment of obstructive sleep apnea in obese adults

机译:芬特明/托吡酯口服延长释放制剂治疗肥胖成人阻塞性睡眠呼吸暂停的随机,双盲,安慰剂对照研究

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Study Objectives: To evaluate safety and efficacy of phentermine 15 mg plus extended-release topiramate 92 mg for treatment of moderate to severe obstructive sleep apnea (OSA) in obese adults. Design: This phase 2, randomized, double-blind, placebo-controlled study included 2-week screening and 28-week treatment periods. Overnight polysomnography was performed at baseline, Week 8, and Week 28. Setting: Single-center study conducted from August 2008 to September 2009. Participants: Forty-five subjects with moderate to severe OSA not receiving positive airway pressure (PAP) treatment with body mass index of 30-40 kg/m2. Interventions: Subjects were randomized to receive placebo (n = 23) or phentermine 15 mg plus extended-release topiramate 92 mg (n = 22). Both groups received lifestyle-modification counseling. Measurements and Results: Primary endpoint, change in apnea-hypopnea index (AHI), significantly favored phentermine 15 mg plus extendedrelease topiramate 92 mg (-31.5 events/h, 95% CI: -40.0, -22.9) over placebo (-16.6 events/h, 95% CI: -25.0, -8.2) at Week 28 (P = 0.0084). At Week 28, there was a 10.2% (95% CI: -12.7, -7.6; 10.8 kg, 95% CI: -13.5, -8.0) mean decrease in weight in the phentermine 15 mg plus extendedrelease topiramate 92 mg group compared with 4.3% (95% CI: -6.6, -2.0; 4.7 kg, 95% CI: -7.2, -2.2) in the placebo group (P = 0.0006) and a positive, significant (P = 0.0003) correlation between percent change in weight and change in AHI. Significant improvements in overnight oxygen saturation and reduction in blood pressure compared with placebo were observed. Phentermine 15 mg plus extended-release topiramate 92 mg was well tolerated with low adverse event rates. Conclusions: Phentermine 15 mg plus extended-release topiramate 92 mg induced significant weight reductions and concomitant improvements in OSA and related symptoms vs placebo. This suggests weight loss mediated by phentermine 15 mg plus extended-release topiramate 92 mg may be useful in treatment of moderate to severe OSA in obese subjects unable or unwilling to comply with PAP treatment.
机译:研究目标:评价芬特明15 mg加缓释托吡酯92 mg治疗肥胖成人中度至重度阻塞性呼吸暂停(OSA)的安全性和有效性。设计:该2期随机,双盲,安慰剂对照研究包括2周筛查和28周治疗期。在基线,第8周和第28周进行隔夜多导睡眠监测。地点:2008年8月至2009年9月进行的单中心研究。参与者:45位中度至重度OSA患者未接受正压通气治疗质量指数为30-40 kg / m2。干预措施:将受试者随机接受安慰剂(n = 23)或芬特明15 mg加缓释托吡酯92 mg(n = 22)。两组均接受了改变生活方式的咨询。测量和结果:主要终点,呼吸暂停低通气指数(AHI)的变化,芬特明15 mg加吡托吡酯缓释92 mg(-31.5事件/小时,95%CI:-40.0,-22.9)明显优于安慰剂(-16.6事件) / h,第28周时(95%CI:-25.0,-8.2)(P = 0.0084)。在第28周时,芬特明15 mg加缓释托吡酯92 mg组的体重平均减少了10.2%(95%CI:-12.7,-7.6; 10.8 kg,95%CI:-13.5,-8.0),与安慰剂组(P = 0.0006)为4.3%(95%CI:-6.6,-2.0; 4.7 kg,95%CI:-7.2,-2.2),且百分比变化之间呈正相关(P = 0.0003)。体重和AHI的变化。观察到与安慰剂相比,夜间血氧饱和度显着改善,血压降低。苯丁胺15 mg加缓释托吡酯92 mg耐受性良好,不良事件发生率低。结论:与安慰剂相比,苯丁胺15毫克加缓释托吡酯92毫克可显着减轻体重,并同时改善OSA和相关症状。这表明由芬特明15 mg加缓释托吡酯92 mg介导的体重减轻可能对无法或不愿接受PAP治疗的肥胖受试者的中重度OSA有用。

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