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Sgemaglutide in type 2 diabetes - is it the best glucagon-like peptide 1 receptor agonist (GLP-1R agonist)?

Expert Opin Drug Metab Toxicol · 2018

Last updated 2026-05-28

Semaglutide is a GLP-1 drug for type 2 diabetes that helps control blood sugar by increasing insulin and reducing glucagon, while also slowing digestion and reducing appetite. In a trial with 3,297 adults (average age 65, baseline blood sugar control of 8.7%, and average weight of 92 kg), once-weekly semaglutide at doses of 0.5 mg or 1 mg reduced cardiovascular risks, though it slightly increased the risk of eye complications called retinopathy.

AI summary of the abstract below.

JournalExpert Opin Drug Metab Toxicol, 2018
Citations12
Relative citation ratio0.52
NIH percentile30
Molecules
Conditions studied Type 2 Diabetes

Abstract

Glucagon-like peptide-1 (GLP-1) is produced by the gut, and in a glucose-dependent manner stimulates insulin secretion while inhibiting glucagon secretion, reduces appetite and energy intake, and delays gastric emptying. The GLP-1R agonist semaglutide has recently been registered to treat type 2 diabetes. Area covered: This review is of semaglutide in type 2 diabetes, and considers which properties of this GLP-1R agonist, may be responsible for its clinical outcome benefits . Expert opinion: The pharmacokinetics of semaglutide make it ideal for once-weekly dosing. SUSTAIN 6 (Trial to Evaluate Cardiovascular and Other Long-term Outcomes With Semaglutide in Subjects With Type 2 Diabetes) showed that semaglutide 0.5 or 1 mg subcutaneously once-weekly reduced cardiovascular outcomes in subjects with type 2 diabetes and cardiovascular disease or risk, mean age 65 years, baseline HbA1c 8.7% and mean body weight of 92 kg. Although, semaglutide may be a useful drug in this population, it increased retinopathy to a small extent and this needs further investigation. Also, it is not known whether semaglutide will improve cardiovascular outcomes in other populations including those with lower ages, HbA1c values, and body weights similar to those included in the unsuccessful clinical outcome trials with the GLP-1R agonists, lixisenatide and exenatide.

Verbatim abstract via PubMed 29439603 ↗