Harnessing GLP‐1 Receptor Agonists for Obesity Treatment: Prospects and Obstacles on the Horizon

医学 利拉鲁肽 2型糖尿病 叙述性评论 肥胖 重症监护医学 生物信息学 临床试验 赛马鲁肽 血糖性 糖尿病 药品 药物开发 全球卫生 药理学 公共卫生 恩帕吉菲 心力衰竭 精密医学 减肥 联合疗法 2型糖尿病 个性化医疗
作者
Riad Mohammed Abdelrahman,Taha Hussein Musa,Ismail Adam Arbab,Mohsen Hussein Suliman,Eltieb Omer Ahmed,Asma Noureldaim Mohamed,Hassan Hussein Musa,Mohammed Jalal,Sahar Ibrahim Gasmallah
出处
期刊:Journal of Obesity [Hindawi Publishing Corporation]
卷期号:2025 (1)
标识
DOI:10.1155/jobe/9919810
摘要

Background Obesity has emerged as a pressing global health challenge, and therapies based on glucagon‐like Peptide 1 receptor agonists (GLP‐1RAs) have transformed its management. Currently, liraglutide, semaglutide, and tirzepatide are FDA‐approved for obesity treatment, while other agents are used off‐label. These drugs not only provide unprecedented efficacy and acceptable safety in weight reduction and glycemic control for patients with obesity and Type 2 diabetes but also hold promise in broader indications, including neurodegenerative disorders, fatty liver disease, dyslipidemia, atherosclerosis, and cardiovascular conditions. Methods This narrative review examined the therapeutic applications of GLP‐1RAs for obesity, emphasizing their efficacy, safety profile, challenges with patient adherence, and limitations. The review also explored emerging innovations such as ultralong‐acting formulations, combination therapies, and the integration of digital health and artificial intelligence in advancing antiobesity drug development. Results GLP‐1RAs represent a paradigm shift in the treatment of obesity and metabolic diseases, with rapidly expanding indications and global uptake. Recent evidence highlights improvements in tolerability, global accessibility, and the potential of novel technologies to optimize patient outcomes. By 2025, GLP‐1RAs are anticipated to receive FDA approval for new indications, such as chronic kidney disease, heart failure with preserved ejection fraction, and metabolic dysfunction–associated steatohepatitis. Novel agents including CagriSema and higher dose oral semaglutide are advancing through clinical trials, while pivotal trial results for orforglipron, mazdutide, retatrutide, and survodutide are anticipated to further expand the therapeutic landscape. At the same time, the arrival of generic liraglutide and evolving insurance coverage are reshaping access and affordability. Conclusion The convergence of pharmacological innovation, digital health strategies, and equitable care initiatives is expected to revolutionize obesity therapeutics in the coming decade. Priorities for future research include sustaining long‐term weight loss, establishing disease‐modifying potential in nonmetabolic disorders, and addressing health equity concerns to ensure broader global benefit.
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