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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 2026-05-28

A 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.

JournalPrim Care Diabetes, 2024
Citations7
Relative citation ratio1.10
NIH percentile54
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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