Characterisation of real-world patients who discontinued a glucagon-like peptide-1 agonist.
Diabetes Obes Metab · 2026
Last updated 2026-05-28In a study of 1,374 adults who started GLP-1 drugs like semaglutide or liraglutide, 31.7% stopped taking them within 180 days. The most common reasons for stopping were side effects (26.8%), concerns about cost (14.4%), and not taking the medication as prescribed (11.2%). People in certain racial groups and those using the drug for weight loss alone were more likely to stop.
AI summary of the abstract below.
| Journal | Diabetes Obes Metab, 2026 |
|---|---|
| Citations | 0 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
AIMS: The objective of this analysis was to identify the 6-month discontinuation rate for GLP-1 analogues, reasons for discontinuation, and characteristics associated with discontinuation.
MATERIALS AND METHODS: This was a retrospective analysis of adult patients who had an initial GLP-1 (semaglutide or liraglutide) dispensed between January 1, 2018 and June 30, 2023. The primary outcome was the 180-day GLP-1 discontinuation rate, and among those who discontinued, identification of documented reasons for discontinuation. The secondary outcome was the identification of patient characteristics associated with GLP-1 discontinuation.
RESULTS: There were 1374 patients included, of whom 436 (31.7%) discontinued GLP-1 therapy. Common reasons for GLP-1 discontinuation included: 26.8% with an adverse drug reaction (ADR), 14.4% with a GLP-1 cost concern, and 11.2% with non-adherence. Asian/Native American/Pacific Islander races (adjusted odds ratio [AOR] 2.51; 95% confidence interval [CI] 1.07-5.91 compared to Whites) and an overweight/obesity indication (AOR 2.46; 95% CI 1.17-5.17 compared to diabetes + overweight/obesity) were associated with GLP-1 discontinuation.
CONCLUSIONS: 180-day GLP-1 discontinuation was prevalent. ADR and cost concerns were primary reasons for discontinuation and health disparities among patients who discontinued were identified. These real-world findings offer patients, providers, and policymakers evidence of potential barriers to GLP-1 persistence.
Verbatim abstract via PubMed 41713959 ↗