首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Two-year sustained weight loss and metabolic benefits with controlled-release phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3 extension study.
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Two-year sustained weight loss and metabolic benefits with controlled-release phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3 extension study.

机译:肥胖和超重成年人(SEQUEL)中的芬特明/托吡酯控释可维持两年的持续减肥和代谢益处:一项随机,安慰剂对照的3期扩展研究。

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BACKGROUND: Obesity is a serious chronic disease. Controlled-release phentermine/topiramate (PHEN/TPM CR), as an adjunct to lifestyle modification, has previously shown significant weight loss compared with placebo in a 56-wk study in overweight and obese subjects with >/=2 weight-related comorbidities. OBJECTIVE: This study evaluated the long-term efficacy and safety of PHEN/TPM CR in overweight and obese subjects with cardiometabolic disease. DESIGN: This was a placebo-controlled, double-blind, 52-wk extension study; volunteers at selected sites continued with original randomly assigned treatment [placebo, 7.5 mg phentermine/46 mg controlled-release topiramate (7.5/46), or 15 mg phentermine/92 mg controlled-release topiramate (15/92)] to complete a total of 108 wk. All subjects participated in a lifestyle-modification program. RESULTS: Of 866 eligible subjects, 676 (78%) elected to continue in the extension. Overall, 84.0% of subjects completed the study, with similar completion rates between treatment groups. At week 108, PHEN/TPM CR was associated with significant, sustained weight loss (intent-to-treat with last observation carried forward; P < 0.0001 compared with placebo); least-squares mean percentage changes from baseline in body weight were -1.8%, -9.3%, and -10.5% for placebo, 7.5/46, and 15/92, respectively. Significantly more PHEN/TPM CR-treated subjects at each dose achieved >/=5%, >/=10%, >/=15%, and >/=20% weight loss compared with placebo (P < 0.001). PHEN/TPM CR improved cardiovascular and metabolic variables and decreased rates of incident diabetes in comparison with placebo. PHEN/TPM CR was well tolerated over 108 wk, with reduced rates of adverse events occurring between weeks 56 and 108 compared with rates between weeks 0 and 56. CONCLUSION: PHEN/TPM CR in conjunction with lifestyle modification may provide a well-tolerated and effective option for the sustained treatment of obesity complicated by cardiometabolic disease. This trial was registered at clinicaltrials.gov as NCT00796367.
机译:背景:肥胖是一种严重的慢性疾病。在56周的超重和肥胖与体重相关合并症的受试者中,与安慰剂相比,控释芬特明/托吡酯(PHEN / TPM CR)作为改善生活方式的辅助手段,先前已显示出明显的体重减轻。目的:本研究评估了PHEN / TPM CR在超重和肥胖的心脏代谢疾病中的长期疗效和安全性。设计:这是一项安慰剂对照,双盲,52周扩展研究。选定地点的志愿者继续接受原始随机分配的治疗[安慰剂,7.5 mg芬特明/ 46 mg控释托吡酯(7.5 / 46)或15 mg芬特明/ 92 mg控释托吡酯(15/92)],以完成总计的108周。所有受试者都参加了改变生活方式的计划。结果:在866名合格受试者中,有676名(78%)选择继续参加延期考试。总体而言,有84.0%的受试者完成了研究,治疗组之间的完成率相似。在第108周时,PHEN / TPM CR与持续的显着体重减轻有关(意向性治疗,最后观察到的结果;与安慰剂相比P <0.0001);安慰剂,7.5 / 46和15/92的相对于基线的最小二乘平均体重百分比变化分别为-1.8%,-9.3%和-10.5%。与安慰剂相比,在每种剂量下,更多的PHEN / TPM CR治疗的受试者体重减轻了> / = 5%,> / = 10%,> / = 15%和> / = 20%(P <0.001)。与安慰剂相比,PHEN / TPM CR改善了心血管和代谢变量,并降低了糖尿病的发病率。对PHEN / TPM CR的耐受性在108周以上良好,与在0和56周之间相比,在56周至108周之间发生的不良事件发生率降低。结论:PHEN / TPM CR与生活方式的改变相结合可以提供良好的耐受性和耐受性。肥胖并发心脏代谢疾病持续治疗的有效选择。该试验已在Clinicaltrials.gov上注册为NCT00796367。

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