Long-term Trends in Antidiabetes Drug Usage in the U.S.: Real-world Evidence in Patients Newly Diagnosed With Type 2 Diabetes
Abstract
OJBECTIVE: To explore temporal trends in antidiabetes drug (ADD) prescribing and intensification patterns, along with glycemic levels and comorbidities, and possible benefits of novel ADDs in delaying the need for insulin initiation in patients diagnosed with type 2 diabetes. RESEARCH DESIGN AND METHODS: Patients with type 2 diabetes aged 18–80 years, who initiated any ADD, were selected (n = 1,023,340) from the U.S. Centricity Electronic Medical Records. Those who initiated second-line ADD after first-line metformin were identified (subcohort 1, n = 357,482); the third-line therapy choices were further explored. RESULTS: From 2005 to 2016, first-line use increased for metformin (60–77%) and decreased for sulfonylureas (20–8%). During a mean follow-up of 3.4 years post metformin, 48% initiated a second ADD at a mean HbA1c of 8.4%. In subcohort 1, although sulfonylurea usage as second-line treatment decreased (60–46%), it remained the most popular second ADD choice. Use increased for insulin (7–17%) and dipeptidyl peptidase-4 inhibitors (DPP-4i) (0.4–21%). The rates of intensification with insulin and sulfonylureas did not decline over the last 10 years. The restricted mean time to insulin initiation was marginally longer in second-line DPP-4i (7.1 years) and in the glucagon-like peptide 1 receptor agonist group (6.6 years) compared with sulfonylurea (6.3 years, P < 0.05). CONCLUSIONS: Most patients initiate second-line therapy at elevated HbA1c levels, with highly heterogeneous clinical characteristics across ADD classes. Despite the introduction of newer therapies, sulfonylureas remained the most popular second-line agent, and the rates of intensification with sulfonylureas and insulin remained consistent over time. The incretin-based therapies were associated with a small delay in the need for therapy intensification compared with sulfonylureas.
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OADs were the most commonly reported treatment discontinued, which is in line with prescription data that shows metformin to be the most commonly prescribed first-line antidiabetic treatment and sulfonylureas the most commonly prescribed second-line antidiabetic treatment.
“OADs were the most commonly reported treatment discontinued, which is in line with prescription data that shows metformin to be the most commonly prescribed first-line antidiabetic treatment and sulfonylureas the most commonly prescribed second-line antidiabetic treatment [10].”
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References 28 · Cited by 250
- Authors
- Montvida, O., Shaw, J., Atherton, J. J., Stringer, F., & Paul, S. K.
- Affiliations
- Queensland University of Technology (AU)
- Baker Heart and Diabetes Institute (AU)
- The University of Queensland (AU)
- Model Answers Pty Ltd, Brisbane, Australia
- The University of Melbourne (AU)
- Corresponding author
- Paul, Sanjoy K.
- Venue
- Diabetes Care
- Publisher
- American Diabetes Association
- Published
- 2017-11-06
- Volume
- 41
- Issue
- 1
- Pages
- 69-78
- ISSN
- 0149-5992 (ISSN-L)
- 1935-5548
- OpenAlex
- W2767408736
- Cited by
- 250
- References
- 28
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 18 · 2023: 23 · 2022: 37 · 2021: 46 · 2020: 56 · 2019: 26 · 2018: 16 · 2017: 1
- FWCI
- 21.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes Care (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- type 2 diabetes, prescribing trends, metformin, sulfonylureas, insulin initiation, DPP-4 inhibitors, GLP-1 receptor agonists, glycemic control, HbA1c, second-line therapy, incretin-based therapy, comorbidities
- MeSH terms
- Glucagon-Like Peptide-1 Receptor, Glucagon-Like Peptide-1 Receptor Agonists, Adolescent, Adult, Aged, Aged, 80 and over, Blood Glucose, Diabetes Mellitus, Type 2, Female, Follow-Up Studies, Humans, Hypoglycemic Agents, Insulin, Longitudinal Studies, Male, Metformin, Middle Aged, Sulfonylurea Compounds, Time Factors, Incretins, Dipeptidyl-Peptidase IV Inhibitors, Young Adult
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