Endocr Pract. 2019 Oct;25(10):1022-1028. doi: 10.4158/EP-2019-0081. Epub 2019 Jun 26.
The effectiveness of anti-obesity medications (AOMs) outside of clinical trials is unclear. The objective of this study was to compare the short-term effectiveness of AOMs in real-world practice. This retrospective study included adults aged ≥18 years, with body mass index ≥30 kg/m or ≥27 kg/m with at least one obesity-related comorbidity who were prescribed phentermine hydrochloride, phenterminetopiramate, bupropion-naltrexone, or lorcaserin for 12 consecutive weeks between 2006 and 2016 at a large tertiary healthcare system. Propensity score-matched cohorts were created for each pair of AOMs. The primary outcomes were percent and absolute weight loss from baseline after 12 weeks. A prediction model was constructed to estimate weight loss with different AOMs based on demographic and clinical data. Of the 3,411 patients included in this study, patients lost an average of 3.45% of body weight from baseline. All AOMs were associated with a significant weight loss from baseline (<.0001). Patients lost the highest percentage of body weight on phentermine hydrochloride (3.75 ± 5.66%), followed by phentermine-topiramate (3.63 ± 5.7%), bupropion-naltrexone (2.66 ± 5.03%), and lorcaserin (1.84 ± 6.69%). In propensity-matched cohorts, patients taking phentermine hydrochloride lost more weight than those taking lorcaserin or bupropion-naltrexone, and patients taking phentermine topiramate lost more weight than patients taking lorcaserin. In real-world practice, AOMs are associated with clinically meaningful weight loss of 2 to 4% after 12 weeks. In this study, phentermine hydrochloride and phentermine topiramate produced the most weight loss. AOMs should be seriously considered as part of the armamentarium to treat patients with obesity. = anti-obesity medication; = body mass index; = electronic medical record; = Food and Drug Administration; = type 2 diabetes.
抗肥胖药物(AOM)在临床试验以外的有效性尚不清楚。本研究的目的是比较 AOM 在真实世界实践中的短期疗效。这项回顾性研究纳入了 2006 年至 2016 年期间在一家大型三级医疗机构接受盐酸苯丁胺、苯丁胺/托吡酯、安非他酮/纳曲酮或lorcaserin 治疗 12 周的年龄≥18 岁、体重指数≥30 kg/m或≥27 kg/m且至少有一种肥胖相关合并症的成年人。为每一对 AOM 创建了倾向评分匹配队列。主要结局是 12 周后从基线开始的体重百分比和绝对减轻量。根据人口统计学和临床数据构建了一个预测模型,以估计不同 AOM 的减重效果。在这项研究中,纳入了 3411 名患者,患者从基线平均减轻了 3.45%的体重。所有 AOM 均与基线显著减重相关(<.0001)。患者服用盐酸苯丁胺后体重减轻的百分比最高(3.75 ± 5.66%),其次是苯丁胺/托吡酯(3.63 ± 5.7%)、安非他酮/纳曲酮(2.66 ± 5.03%)和lorcaserin(1.84 ± 6.69%)。在倾向评分匹配队列中,服用盐酸苯丁胺的患者比服用 lorcaserin 或安非他酮/纳曲酮的患者体重减轻更多,服用苯丁胺/托吡酯的患者比服用 lorcaserin 的患者体重减轻更多。在真实世界实践中,AOM 在 12 周后可使体重减轻 2%至 4%,具有临床意义。在本研究中,盐酸苯丁胺和苯丁胺/托吡酯的减重效果最明显。AOM 应作为治疗肥胖症患者的武器库的一部分认真考虑。AOM=抗肥胖药物;BMI=体重指数;EMR=电子病历;FDA=美国食品和药物管理局;2 型糖尿病。