Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland.
Section on Growth and Obesity, Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
JAMA. 2014 Jan 1;311(1):74-86. doi: 10.1001/jama.2013.281361.
IMPORTANCE: Thirty-six percent of US adults are obese, and many cannot lose sufficient weight to improve health with lifestyle interventions alone. OBJECTIVE: To conduct a systematic review of medications currently approved in the United States for obesity treatment in adults. We also discuss off-label use of medications studied for obesity and provide considerations for obesity medication use in clinical practice. EVIDENCE REVIEW: A PubMed search from inception through September 2013 was performed to find meta-analyses, systematic reviews, and randomized, placebo-controlled trials for currently approved obesity medications lasting at least 1 year that had a primary or secondary outcome of body weight change, included at least 50 participants per group, reported at least 50% retention, and reported results on an intention-to-treat basis. Studies of medications approved for other purposes but tested for obesity treatment were also reviewed. FINDINGS: Obesity medications approved for long-term use, when prescribed with lifestyle interventions, produce additional weight loss relative to placebo ranging from approximately 3% of initial weight for orlistat and lorcaserin to 9% for top-dose (15/92 mg) phentermine plus topiramate-extended release at 1 year. The proportion of patients achieving clinically meaningful (at least 5%) weight loss ranges from 37% to 47% for lorcaserin, 35% to 73% for orlistat, and 67% to 70% for top-dose phentermine plus topiramate-extended release. All 3 medications produce greater improvements in many cardiometabolic risk factors than placebo, but no obesity medication has been shown to reduce cardiovascular morbidity or mortality. Most prescriptions are for noradrenergic medications, despite their approval only for short-term use and limited data for their long-term safety and efficacy. CONCLUSIONS AND RELEVANCE: Medications approved for long-term obesity treatment, when used as an adjunct to lifestyle intervention, lead to greater mean weight loss and an increased likelihood of achieving clinically meaningful 1-year weight loss relative to placebo. By discontinuing medication in patients who do not respond with weight loss of at least 5%, clinicians can decrease their patients' exposure to the risks and costs of drug treatment when there is little prospect of long-term benefit.
重要性:36%的美国成年人肥胖,许多人无法仅通过生活方式干预减轻足够的体重来改善健康状况。
目的:对目前在美国批准用于治疗成人肥胖的药物进行系统回顾。我们还讨论了用于肥胖研究的药物的标签外使用,并提供了在临床实践中使用肥胖药物的注意事项。
证据回顾:从开始到 2013 年 9 月,进行了一次 PubMed 搜索,以找到持续至少 1 年的、主要或次要结局为体重变化的、至少 50 名参与者/组的、报告至少 50%保留率的、并基于意向治疗报告结果的目前批准用于肥胖治疗的药物的荟萃分析、系统评价和随机、安慰剂对照试验。还审查了用于其他目的但用于肥胖治疗测试的药物的研究。
发现:长期使用批准用于肥胖治疗的药物,与生活方式干预相结合,相对于安慰剂可额外减轻约 3%的初始体重(奥利司他和lorcaserin)至 9%(top-dose [15/92mg] phentermine加 topiramate-延伸释放)在 1 年时。达到临床意义(至少 5%)体重减轻的患者比例范围为 lorcaserin 为 37%至 47%,orlistat 为 35%至 73%,top-dose phentermine加 topiramate-延伸释放为 67%至 70%。所有 3 种药物在许多心血管代谢风险因素方面的改善都优于安慰剂,但没有一种肥胖药物已被证明可降低心血管发病率或死亡率。尽管大多数处方都是针对去甲肾上腺素能药物,但这些药物仅批准短期使用,并且长期安全性和疗效数据有限。
结论和相关性:长期肥胖治疗批准的药物,当用作生活方式干预的辅助手段时,相对于安慰剂可导致更大的平均体重减轻,并增加实现临床意义上的 1 年体重减轻的可能性。通过停止对体重减轻至少 5%的患者的药物治疗,可以减少患者对药物治疗风险和成本的暴露,因为长期获益的前景很小。
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