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A real-world study published in Diabetes, Obesity and Metabolism found that adults with T2DM were more likely to remain on SGLT2i therapy than on GLP-1 RAs.

Using Humana Healthcare Research claims data from January 2018 to June 2022, investigators compared 12-month treatment patterns among 22,167 GLP-1 RA and 22,267 SGLT2i initiators. Persistence, defined as continuous therapy without a >45-day gap, was higher for SGLT2i users (47% vs 37.6%). GLP-1 RA initiators were more likely to discontinue therapy (HR = 1.39, p < 0.001).

Treatment augmentation, defined as the initiation of a new glucose-lowering class, was also more common with SGLT2 inhibitors (27.4% vs 23.4%). Subgroup analyses in patients with cardiovascular disease and obesity showed similar patterns.

These findings suggest that the oral route, favorable tolerability, and lower cost may contribute to stronger adherence with SGLT2i therapy. Addressing patient-specific barriers could further enhance persistence and long-term glycemic outcomes.

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Key highlights
  • In a matched cohort of more than 44,000 adults with type 2 diabetes (T2DM), one-year persistence was 47% for sodium–glucose cotransporter-2 (SGLT2) inhibitors and 38% for glucagon-like peptide-1 (GLP-1) receptor agonists (p < 0.001).
  • GLP-1 RA users were 39% more likely to discontinue therapy (HR = 1.39, p < 0.001).
  • Treatment augmentation occurred in 27.4% of SGLT2i users versus 23.4% of GLP-1 RA users.
  • Trends were consistent across cardiovascular and obesity subgroups.
Source

Bowe A, Hayes M, John I, Diaz M, Dixon S, Poonawalla I. Glucagon-like peptide-1 receptor agonist versus sodium-glucose cotransporter-2 inhibitor persistence in Medicare Advantage beneficiaries with type 2 diabetes, cardiovascular risk, and obesity. Diabetes Obes Metab. Published online October 30, 2025. doi:10.1111/dom.70219

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SGLT2 Inhibitors Show Greater Treatment Persistence Than GLP-1 RAs in T2DM
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Real-world claims analysis finds better adherence and treatment augmentation with SGLT2 inhibitors

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