Kentucky Research Group, Louisville, KY 40217, USA.
Sleep. 2012 Nov 1;35(11):1529-39. doi: 10.5665/sleep.2204.
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.
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.
Single-center study conducted from August 2008 to September 2009.
Forty-five subjects with moderate to severe OSA not receiving positive airway pressure (PAP) treatment with body mass index of 30-40 kg/m(2).
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.
Primary endpoint, change in apnea-hypopnea index (AHI), significantly favored phentermine 15 mg plus extended-release 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 extended-release 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.
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.
评估安非他酮 15mg 联合托吡酯控释片 92mg 治疗肥胖合并中重度阻塞性睡眠呼吸暂停(OSA)患者的安全性和疗效。
这是一项为期 28 周的、随机、双盲、安慰剂对照的 II 期临床试验,包括 2 周的筛选期和 28 周的治疗期。所有患者在基线、第 8 周和第 28 周时均接受整夜多导睡眠监测。
单中心研究,于 2008 年 8 月至 2009 年 9 月进行。
45 名肥胖合并中重度 OSA 患者,BMI 为 30-40kg/m²,未接受过正压通气(PAP)治疗。
患者被随机分为安慰剂组(n=23)和安非他酮 15mg 联合托吡酯控释片 92mg 组(n=22)。两组患者均接受生活方式干预。
主要终点是呼吸暂停低通气指数(AHI)的变化,安非他酮 15mg 联合托吡酯控释片 92mg 组在第 28 周时的 AHI 较安慰剂组显著下降(-31.5 次/h,95%CI:-40.0,-22.9)(P=0.0084)。第 28 周时,安非他酮 15mg 联合托吡酯控释片 92mg 组的体重较基线平均下降 10.2%(95%CI:-12.7,-7.6;10.8kg,95%CI:-13.5,-8.0),而安慰剂组仅下降 4.3%(95%CI:-6.6,-2.0;4.7kg,95%CI:-7.2,-2.2)(P=0.0006),并且体重减轻的百分比与 AHI 的变化呈显著正相关(P=0.0003)。与安慰剂组相比,安非他酮 15mg 联合托吡酯控释片 92mg 组患者的夜间血氧饱和度显著升高,血压显著降低。安非他酮 15mg 联合托吡酯控释片 92mg 耐受性良好,不良事件发生率低。
安非他酮 15mg 联合托吡酯控释片 92mg 可显著减轻体重,同时改善 OSA 及其相关症状,这表明安非他酮 15mg 联合托吡酯控释片 92mg 介导的体重减轻可能对肥胖合并中重度 OSA 患者有用,尤其是对不能或不愿接受 PAP 治疗的患者。