GLP-1 receptor agonist (GLP-1RA)SUSTAIN and PIONEER trialsSemaglutidebiliary disease (cholelithiasis)gastrointestinal adverse events
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Abstract (AI)
The glucagon-like peptide-1 receptor agonist (GLP-1RA) semaglutide is the most recently approved agent of this drug class, and the only GLP-1RA currently available as both subcutaneous and oral formulation. While GLP-1RAs effectively improve glycemic control and cause weight loss, potential safety concerns have arisen over the years. For semaglutide, such concerns have been addressed in the extensive phase 3 registration trials including cardiovascular outcome trials for both subcutaneous (SUSTAIN: Semaglutide Unabated Sustainability in Treatment of Type 2 Diabetes) and oral (PIONEER: Peptide InnOvatioN for the Early diabEtes tReatment) semaglutide and are being studied in further trials and registries, including real world data studies. In the current review we discuss the occurrence of adverse events associated with semaglutide focusing on hypoglycemia, gastrointestinal side effects, pancreatic safety (pancreatitis and pancreatic cancer), thyroid cancer, gallbladder events, cardiovascular aspects, acute kidney injury, diabetic retinopathy (DRP) complications and injection-site and allergic reactions and where available, we highlight potential underlying mechanisms. Furthermore, we discuss whether effects are specific for semaglutide or a class effect. We conclude that semaglutide induces mostly mild-to-moderate and transient gastrointestinal disturbances and increases the risk of biliary disease (cholelithiasis). No unexpected safety issues have arisen to date, and the established safety profile for semaglutide is similar to that of other GLP-1RAs where definitive conclusions for pancreatic and thyroid cancer cannot be drawn at this point due to low incidence of these conditions. Due to its potent glucose-lowering effect, patients at risk for deterioration of existing DRP should be carefully monitored if treated with semaglutide, particularly if also treated with insulin. Given the beneficial metabolic and cardiovascular actions of semaglutide, and the low risk for severe adverse events, semaglutide has an overall favorable risk/benefit profile for patient with type 2 diabetes.
Key Findings
1
Because of potent glucose lowering, semaglutide may worsen existing diabetic retinopathy risk, so patients with DRP—especially those on insulin—should be carefully monitored.
2
No unexpected safety issues have emerged and semaglutide's safety profile is similar to other GLP-1 receptor agonists, though definitive conclusions on pancreatic and thyroid cancer risk cannot be drawn due to low incidence.
3
Semaglutide commonly causes mostly mild-to-moderate, transient gastrointestinal adverse events.
4
Semaglutide increases the risk of biliary disease, specifically cholelithiasis.
5
Semaglutide is available in both subcutaneous and oral formulations and has been evaluated in extensive phase 3 trials (SUSTAIN, PIONEER) and ongoing registries/real-world studies.
Research Object
Semaglutide (GLP-1 receptor agonist, subcutaneous and oral formulations)
Research Subject
Safety profile and occurrence of adverse events associated with semaglutide, including hypoglycemia, gastrointestinal effects, pancreatic safety (pancreatitis and pancreatic cancer), thyroid cancer, gallbladder events, cardiovascular effects, acute kidney injury, diabetic retinopathy complications, and injection-site/allergic reactions, and whether these are semaglutide-specific or class effects
Publication Details
Publication Date
2021-07-07
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