Future Medications for Obesity and Clinical Implications

医学 胰淀素 减肥 赛马鲁肽 肥胖 临床试验 药物开发 2型糖尿病 糖尿病 重症监护医学 生物信息学 药品 药理学 内科学 内分泌学 利拉鲁肽 小岛 生物
作者
W. Timothy Garvey
出处
期刊:Diabetes Spectrum [American Diabetes Association]
卷期号:37 (4): 325-334 被引量:1
标识
DOI:10.2337/dsi24-0004
摘要

Semaglutide and tirzepatide have recently been approved for obesity and found to achieve ≥15% weight loss in clinical trials. These drugs have been referred to as second-generation medications because the unprecedented degree of weight loss they afford is sufficient to treat or prevent a broad array of obesity complications and related diseases. Many other medications are in development based on the actions of nutrient-regulated hormones (NRHs), including mono-, dual-, and triple-receptor agonists/antagonists for glucagon-like peptide 1, glucose-dependent insulinotropic polypeptide, amylin, peptide tyrosine-tyrosine, and glucagon. Clinical trial evidence is accumulating that these medications ameliorate multiple biomechanical, metabolic, and vascular complications of obesity. These tools enable a comprehensive complications-centric approach to care within the contextual framework of the diagnostic term adiposity-based chronic disease (ABCD). The potential to reduce patient suffering and the huge social burden of ABCD is profound. The current era of drug development based on NRHs could represent a landmark in the history of medicine provided that societies ensure access to these medications for the patients who need them.

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