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肠促胰岛素激素激动剂:肥胖管理的当前及新兴药物治疗方法。

Incretin hormone agonists: Current and emerging pharmacotherapy for obesity management.

作者信息

Alhomoud Ibrahim S, Talasaz Azita H, Chandrasekaran Preethi, Brown Roy, Mehta Anurag, Dixon Dave L

机构信息

Department of Pharmacy Practice, College of Pharmacy, Qassim University, Qassim, Saudi Arabia.

Department of Pharmacy, New York-Presbyterian Hospital/Columbia University Irving Medical Center, New York, New York, USA.

出版信息

Pharmacotherapy. 2024 Sep;44(9):738-752. doi: 10.1002/phar.4607. Epub 2024 Sep 3.

Abstract

Obesity continues to be a significant global health challenge, affecting over 800 million individuals worldwide. Traditional management strategies, including dietary, exercise, and behavioral interventions, often result in insufficient and unsustainable weight loss. Lifestyle modification remains the cornerstone of obesity management, providing the foundation for other strategies. While options such as bariatric surgery remain an effective intervention for severe obesity, it is associated with its own set of risks and is typically reserved for patients who have not achieved the desired results with pharmacotherapy and lifestyle interventions. Incretin hormone agonists represent a significant advancement in the pharmacotherapy of obesity, offering substantial weight reduction and cardiometabolic benefits. Agents like liraglutide, semaglutide, and tirzepatide supported by key clinical trials such as Satiety and Clinical Adipose Liraglutide Evidence (SCALE), Semaglutide Treatment Effect in People with Obesity (STEP) program trials, and Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1) have demonstrated remarkable efficacy in promoting weight loss and improving metabolic outcomes. Additionally, novel therapies, including dual and triple incretin agonists, are under investigation and hold the potential for further advancements in obesity treatment. These novel therapies can be categorized by their mechanisms of action and route of administration into oral glucagon-like peptide-1 (GLP-1) receptor agonists, triple agonists (targeting GLP-1, glucose-dependent insulinotropic polypeptide [GIP], and glucagon receptors), and glucagon receptor-GLP-1 receptor co-agonists. Other innovative approaches include oral GIP-GLP-1 receptor co-agonists, and the combination of long-acting amylin receptor agonists with GLP-1 receptor agonists. The ongoing development of incretin-based therapies and the expanding availability of currently available agents are expected to enhance clinical outcomes further and reduce the burden of obesity-related health complications. This review aims to discuss the mechanisms and efficacy of current and emerging incretin hormone agonists for obesity management.

摘要

肥胖仍然是一项重大的全球健康挑战,全球有超过8亿人受其影响。传统的管理策略,包括饮食、运动和行为干预,往往导致体重减轻不足且不可持续。生活方式的改变仍然是肥胖管理的基石,为其他策略提供基础。虽然诸如减肥手术等选择仍然是重度肥胖的有效干预措施,但其本身存在一系列风险,通常仅适用于药物治疗和生活方式干预未达到预期效果的患者。肠促胰岛素激素激动剂代表了肥胖药物治疗的重大进展,可实现显著的体重减轻并带来心血管代谢益处。诸如利拉鲁肽、司美格鲁肽和替尔泊肽等药物,在饱腹感与临床脂肪利拉鲁肽证据(SCALE)、司美格鲁肽治疗肥胖症患者的疗效(STEP)项目试验以及替尔泊肽每周一次治疗肥胖症(SURMOUNT - 1)等关键临床试验的支持下,已在促进体重减轻和改善代谢结果方面显示出显著疗效。此外,包括双靶点和三靶点肠促胰岛素激动剂在内的新型疗法正在研究中,有望在肥胖治疗方面取得进一步进展。这些新型疗法可根据其作用机制和给药途径分为口服胰高血糖素样肽 - 1(GLP - 1)受体激动剂、三靶点激动剂(靶向GLP - 1、葡萄糖依赖性促胰岛素多肽[GIP]和胰高血糖素受体)以及胰高血糖素受体 - GLP - 1受体共同激动剂。其他创新方法包括口服GIP - GLP - 1受体共同激动剂,以及长效胰淀素受体激动剂与GLP - 1受体激动剂的联合使用。基于肠促胰岛素的疗法的持续研发以及现有药物可用性的不断扩大,有望进一步改善临床结局并减轻肥胖相关健康并发症的负担。本综述旨在讨论当前和新兴的肠促胰岛素激素激动剂在肥胖管理中的作用机制和疗效。

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