Grant Medical College and Consulting Endocrinologist, Lilavati Hospital, Mumbai, India.
Department of Endocrinology, PGIMS, Rohtak, Haryana, India.
Diabetes Metab Syndr. 2022 Jun;16(6):102508. doi: 10.1016/j.dsx.2022.102508. Epub 2022 May 23.
Despite their established benefits, glucagon-like peptide-1 receptor agonists (GLP-1 RAs) remain underutilized for type 2 diabetes mellitus (T2DM) management, which indicates that subcutaneous injection is an unfavorable mode of delivery from the patient's perspective. This review summarizes existing challenges related to medication adherence and the use of antihyperglycemia injectables, revisits the established safety and efficacy of oral semaglutide, and explores its features and considerations for use among the Indian T2DM population.
We performed a literature search using MEDLINE and the National Institutes of Health Clinical Trials Registry from July 1, 2016, to July 1, 2021, to identify publications on oral semaglutide approval, T2DM treatment guidelines, and clinical evidence for oral drug formulation.
Oral semaglutide is the first oral GLP-1 RA approved for T2DM patients based on phase 3, randomized PIONEER trials. The multitargeted action of this drug offers glycemic control, weight control, and cardiovascular, renal, and additional benefits, including patient convenience and enhanced medication adherence. In addition to achieving glycemic control, the cost of semaglutide is reported to be lower than other GLP-1 RA in the West, thus potentially mitigating the economic burden that appears to be high among the Indian population.
Currently, there is no data available on oral semaglutide in Indian clinical settings. However, significant improvements in glycemic control, cardiac and renal benefits, as well as weight loss across clinical trials should encourage clinicians to prioritize oral semaglutide over other antidiabetic agents.
尽管胰高血糖素样肽-1 受体激动剂(GLP-1 RAs)已被证实具有益处,但它们在 2 型糖尿病(T2DM)管理中的应用仍不充分,这表明从患者角度来看,皮下注射不是一种理想的给药方式。本综述总结了与药物依从性和抗高血糖注射剂使用相关的现有挑战,回顾了口服司美格鲁肽的既定安全性和有效性,并探讨了其在印度 T2DM 人群中的特点和使用注意事项。
我们使用 MEDLINE 和美国国立卫生研究院临床试验注册中心进行了文献检索,检索时间为 2016 年 7 月 1 日至 2021 年 7 月 1 日,以确定关于口服司美格鲁肽批准、T2DM 治疗指南和口服药物制剂临床证据的出版物。
口服司美格鲁肽是第一种基于 3 期随机 PIONEER 试验批准用于 T2DM 患者的口服 GLP-1 RA。该药物的多靶点作用可实现血糖控制、体重控制以及心血管、肾脏和其他获益,包括患者便利性和增强的药物依从性。除了实现血糖控制外,司美格鲁肽的成本据报道低于西方的其他 GLP-1 RA,因此可能减轻印度人群中似乎较高的经济负担。
目前,印度临床环境中尚无关于口服司美格鲁肽的数据。然而,临床试验中在血糖控制、心脏和肾脏获益以及体重减轻方面的显著改善,应鼓励临床医生将口服司美格鲁肽作为其他抗糖尿病药物的首选。