赛马鲁肽
医学
利拉鲁肽
杜拉鲁肽
胰高血糖素样肽1受体
药理学
口服
内科学
糖尿病
兴奋剂
胰高血糖素样肽-1
2型糖尿病
艾塞那肽
内分泌学
受体
作者
John D. Bucheit,Lauren G. Pamulapati,Nicole Carter,Kevin J. Malloy,Dave L. Dixon,Evan M. Sisson
出处
期刊:Diabetes Technology & Therapeutics
[Mary Ann Liebert]
日期:2019-08-22
卷期号:22 (1): 10-18
被引量:116
标识
DOI:10.1089/dia.2019.0185
摘要
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.
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