Adherence and persistence among people with type 2 diabetes newly initiating oral semaglutide versus DPP-4is in a US real-world setting.
Prim Care Diabetes · 2024
Last updated 2026-05-28A study compared people with type 2 diabetes who started taking oral semaglutide (a GLP-1 drug) to those who started taking DPP-4 inhibitors. After one year, 41.6% of the semaglutide group and 42.9% of the DPP-4 inhibitor group were considered adherent, while 45.0% and 46.3% remained on their medication for at least nine months, showing no significant difference between the two groups.
AI summary of the abstract below.
| Journal | Prim Care Diabetes, 2024 |
|---|---|
| Citations | 7 |
| Relative citation ratio | 1.10 |
| NIH percentile | 54 |
| Molecules | semaglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
AIMS: To investigate real-world treatment adherence and persistence in people with type 2 diabetes newly initiating oral semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1 RA), or a dipeptidyl peptidase-4 inhibitor (DPP-4i).
METHODS: This retrospective cohort study used the Merative™ MarketScan® Commercial and Medicare databases. Index date was the first fill for the cohort medication. Adherence was defined as proportion of days covered (PDC) over the 12-month post-index period ('adherent' = ≥0.8). Persistence was number of days until discontinuation, based on a 45-day gap. Results were compared between cohorts using inverse probability treatment weighting.
RESULTS: Oral semaglutide (n=5485) and DPP-4i (n=4980) cohorts had similar percentages of people who were adherent (PDC ≥0.8; 41.6 % vs. 42.9 %; P = 0.182) and persistent for ≥9 months (45.0 % vs. 46.3 %; P = 0.185). The DPP-4i cohort used significantly more anti-diabetic medication (ADM) classes over the post-index period (mean±SD: 2.6±1.0 vs. 2.9±1.1, P < 0.001), with 23.2 % filling a GLP-1 RA in the post-period.
CONCLUSIONS: Adherence and persistence were similar between cohorts. However, there are potential benefits to prescribing oral semaglutide over DPP-4is, including reduced need for additional ADM.
Verbatim abstract via PubMed 38991896 ↗
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