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口服司美格鲁肽:首个口服胰高血糖素样肽-1 受体激动剂的综述。

Oral Semaglutide: A Review of the First Oral Glucagon-Like Peptide 1 Receptor Agonist.

机构信息

Department of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University School of Pharmacy, Richmond, Virginia.

出版信息

Diabetes Technol Ther. 2020 Jan;22(1):10-18. doi: 10.1089/dia.2019.0185. Epub 2019 Oct 1.

Abstract

Glucagon-like peptide 1 receptor agonists (GLP-1 RAs) are highly effective at lowering hemoglobin A1c (HbA1c) and facilitating weight loss. Four agents in the GLP-1 RA class, albiglutide, liraglutide, dulaglutide, and semaglutide, also have cardioprotective effects. However, subcutaneous administration of these agents remains a major reason for their underutilization. A new coformulation of semaglutide with sodium N-[8-(2-hydroxybenzoyl) amino caprylate (SNAC) is the first oral GLP-1 RA reviewed by the U.S. Food and Drug Administration (FDA). The SNAC technology prevents destruction of semaglutide in the stomach and facilitates transcellular absorption through the gastric membrane enabling semaglutide to reach systemic circulation intact. The oral formulation of semaglutide was studied in the PIONEER trials, demonstrating similar efficacy to the presently available GLP-1 RAs with regard to HbA1c lowering and weight loss. Although the PIONEER 6 trial suggests positive effects on cardiovascular mortality with oral semaglutide, these benefits may not fully be appreciated until the completion of the SOUL trial.

摘要

胰高血糖素样肽 1 受体激动剂(GLP-1 RAs)在降低血红蛋白 A1c(HbA1c)和促进体重减轻方面非常有效。GLP-1 RA 类中的四种药物,阿必鲁肽、利拉鲁肽、度拉糖肽和司美格鲁肽,也具有心脏保护作用。然而,这些药物的皮下给药仍是其未被充分利用的主要原因。司美格鲁肽与钠 N-[8-(2-羟基苯甲酰基)氨基辛酸盐(SNAC)的新复方制剂是美国食品和药物管理局(FDA)审查的第一个口服 GLP-1 RA。SNAC 技术可防止司美格鲁肽在胃中被破坏,并通过胃膜促进细胞间吸收,使司美格鲁肽完整地进入全身循环。口服司美格鲁肽在 PIONEER 试验中进行了研究,在降低 HbA1c 和减轻体重方面,其疗效与目前可用的 GLP-1 RAs 相似。尽管 PIONEER 6 试验表明口服司美格鲁肽对心血管死亡率有积极影响,但这些益处可能要等到 SOUL 试验完成后才能完全体现出来。

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