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获得可负担的GLP-1肥胖症药物:美国指导市场行动和政策解决方案的策略

Affordable access to GLP-1 obesity medications: strategies to guide market action and policy solutions in the US.

作者信息

Pearson Steven D, Whaley Christopher M, Emond Sarah K

机构信息

Institute for Clinical & Economic Review, Boston, MA 02108, USA.

Brown University, Providence, RI 02912, USA.

出版信息

J Comp Eff Res. 2025 Sep;14(9):e250083. doi: 10.57264/cer-2025-0083. Epub 2025 Jul 11.

DOI:10.57264/cer-2025-0083
PMID:40641455
Abstract

Glucagon-like peptide 1 receptor agonists and glucagon-like peptide 1/gastric inhibitory polypeptide receptor agonists offer weight reduction and associated health benefits that, if sustained over time, have the potential to markedly improve population health. However, over 40% of US adults have obesity, translating into more than 100 million potential new users of obesity medications. Standing in the way of the major opportunity to improve health for these individuals is the massive and likely ongoing cost of treating such a large segment of the population, even though use of the treatments is estimated to be cost-effective over a lifetime. This paper analyzes the range of emerging market approaches and policy reforms that have the potential to help the broader US health system achieve affordable and equitable access to these medications, and the relative advantages, barriers and possible unintended consequences of each approach. We seek to present policymakers and industry leaders with insights and lessons learned from experts while offering a menu of options for the future that will help all stakeholders play an active part in an innovative future of pricing, coverage and payment for new obesity medications.

摘要

胰高血糖素样肽-1受体激动剂和胰高血糖素样肽-1/胃抑制多肽受体激动剂具有减轻体重及相关健康益处,若长期维持,有可能显著改善人群健康。然而,超过40%的美国成年人患有肥胖症,这意味着超过1亿潜在的肥胖症药物新用户。尽管据估计使用这些治疗方法在一生中具有成本效益,但治疗如此庞大的人群所需的巨大且可能持续的成本,成为改善这些人健康这一重大机遇的障碍。本文分析了一系列新兴市场方法和政策改革,这些方法有可能帮助更广泛的美国医疗系统以可承受且公平的方式获得这些药物,以及每种方法的相对优势、障碍和可能产生的意外后果。我们旨在向政策制定者和行业领导者提供从专家那里获得的见解和经验教训,同时提供一份未来的选择清单,这将有助于所有利益相关者积极参与肥胖症新药定价、覆盖范围和支付的创新未来。

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本文引用的文献

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Glucagon-Like Peptide-1 Receptor Agonists and Risk of Neovascular Age-Related Macular Degeneration.胰高血糖素样肽-1受体激动剂与新生血管性年龄相关性黄斑变性的风险
JAMA Ophthalmol. 2025 Jun 5. doi: 10.1001/jamaophthalmol.2025.1455.
2
Compounded GLP-1 and Dual GIP/GLP-1 Receptor Agonists: A Statement from the American Diabetes Association.复合胰高血糖素样肽-1及双重葡萄糖依赖性促胰岛素多肽/胰高血糖素样肽-1受体激动剂:美国糖尿病协会声明
Diabetes Care. 2025 Feb 1;48(2):177-181. doi: 10.2337/dci24-0091.
3
Approach to the Patient With Thyroid Nodules: Considering GLP-1 Receptor Agonists.
甲状腺结节患者的诊疗方法:考虑胰高血糖素样肽-1受体激动剂
J Clin Endocrinol Metab. 2025 May 19;110(6):e2080-e2087. doi: 10.1210/clinem/dgae722.
4
Modeling health risks using neural network ensembles.使用神经网络集成模型进行健康风险建模。
PLoS One. 2024 Oct 9;19(10):e0308922. doi: 10.1371/journal.pone.0308922. eCollection 2024.
5
Muscle matters: the effects of medically induced weight loss on skeletal muscle.肌肉的重要性:医学诱导体重减轻对骨骼肌的影响
Lancet Diabetes Endocrinol. 2024 Nov;12(11):785-787. doi: 10.1016/S2213-8587(24)00272-9. Epub 2024 Sep 9.
6
International coverage of GLP-1 receptor agonists: a review and ethical analysis of discordant approaches.胰高血糖素样肽-1受体激动剂的国际覆盖范围:对不一致方法的综述与伦理分析
Lancet. 2024 Aug 31;404(10455):902-906. doi: 10.1016/S0140-6736(24)01356-4. Epub 2024 Aug 16.
7
Expanding Medicare Coverage Of Anti-Obesity Medicines Could Increase Annual Spending By $3.1 Billion To $6.1 Billion.扩大医疗保险对抗肥胖药物的覆盖范围可能会使年度支出增加 31 亿美元至 61 亿美元。
Health Aff (Millwood). 2024 Sep;43(9):1254-1262. doi: 10.1377/hlthaff.2024.00356. Epub 2024 Aug 15.
8
An efficient approach to expand equitable access to antiobesity medications: deprescribing after weight loss plateau.一种扩大抗肥胖药物公平可及性的有效方法:减肥平台期后减药。
Am J Manag Care. 2024 Aug;30(8):348-350. doi: 10.37765/ajmc.2024.89586.
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JAMA Netw Open. 2024 Jun 3;7(6):e2416775. doi: 10.1001/jamanetworkopen.2024.16775.
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Real-world persistence and adherence to glucagon-like peptide-1 receptor agonists among obese commercially insured adults without diabetes.肥胖且有商业保险的非糖尿病成年人中胰高血糖素样肽-1受体激动剂在现实世界中的持续性和依从性
J Manag Care Spec Pharm. 2024 Aug;30(8):860-867. doi: 10.18553/jmcp.2024.23332. Epub 2024 May 8.