Risk of insulin initiation with sodium-glucose cotransporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes mellitus: A real-world claims database study in Japan


Here are the Risk of insulin initiation with sodium-glucose cotransporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes mellitus: A real-world claims database study in Japan journals presenting the latest research across various disciplines. From social sciences to technology, each article is expected to provide valuable insights to our readers.

Why is insulin dangerous, risk of rain 2 crossplay, consequences of incorrect use of insulin, insulin effect on sodium, risk of rain items, if im receiving too much insulin, risk of rain 2 item list, why are high levels of insulin dangerous, risk of taking insulin, diabetes and sodium levels.

Risk of insulin initiation with sodium-glucose cotransporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes mellitus: A real-world claims database study in Japan

Aims: Insulin therapy is a cornerstone in type 2 diabetes mellitus (T2DM) management, but its use is associated with several barriers, including hypoglycaemia, fear of injections and high costs. We compared the risk of insulin initiation and other treatment intensification between patients with T2DM newly treated with a sodium-glucose cotransporter-2 inhibitor (SGLT2i) versus those newly treated with a dipeptidyl peptidase-4 inhibitor (DPP4i). Materials and

Methods: This Japanese retrospective cohort study was conducted between 1 January 2015 and 31 March 2023 using the JMDC Claims Database. Patients with T2DM newly treated with an SGLT2i or a DPP4i were matched 1:1 using propensity score (n = 18 488 each). Incidence rates (IR) of insulin initiation, other antidiabetic drugs (OAD) and antihypertensive drugs added onto baseline treatment were calculated for each treatment group. Hazard ratios (HR) and 95% confidence intervals (CI) were calculated using a Cox proportional hazards model.

Results: The IR of insulin initiation was 0.95 and 2.12 per 1000 person-years in the SGLT2i and DPP4i groups, respectively, with significantly lower risk in the SGLT2i group than in the DPP4i group (HR 0.46, 95% CI: 0.28–0.74, p = 0.001). The risks of OAD (HR 0.66, 95% CI: 0.64–0.69, p < 0.001) and antihypertensive drugs (HR 0.90, 95% CI: 0.85–0.95, p < 0.001) added onto baseline treatment were lower in the SGLT2i group than in the DPP4i group. Conclusions: The risk of insulin initiation was lower in patients with T2DM newly treated with an SGLT2i than in those newly treated with a DPP4i. SGLT2i may reduce or delay the need for insulin therapy. © 2025 The Author(s). Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

Authors : Suzuki R.; Shoji S.; Yoshinaga Y.; Kosakai Y.; Shintani-Tachi M.

Source : John Wiley and Sons Inc

Article Information

Year 2025
Type Article
DOI 10.1111/dom.16188
ISSN 14628902
Volume

You can download the article here


If You have any problem, contact us here


Support Us:

Download Now Buy me a coffee Request Paper Here