Use of SGLT2 Inhibitors for Diabetes and Risk of Infection: Analysis Using General Practice Records from the NPS MedicineWise MedicineInsight Program
Overview
Affiliations
Aims: To explore the feasibility of MedicineInsight data to support risk management plan evaluation, focusing on sodium glucose co-transporter 2 (SGLT2) inhibitors for type 2 diabetes.
Methods: A retrospective study using de-identified electronic general practitioner records. Patients who initiated SGLT2 inhibitor between 1 Jan 2012 to 1 Sep 2015 were compared to patients who initiated dipeptidyl peptidase 4 (DPP-4) inhibitors. The two cohorts were followed-up for six months. Risk of urinary-tract (UT) and genital infections was evaluated. The indication for use of SGLT2 inhibitors, recommended prior diabetes therapies and recommended monitoring were investigates.
Results: There were 1977 people in the SGLT2 cohort (with 93% initiated on dapagliflozin) and 1964 people in the DPP-4 cohort. Of the SGLT2 initiators, 54% had a documented indication for use as type 2 diabetes; 86% had used metformin and/or a sulfonylurea in the prior 12months. Renal function monitoring was documented for only 25% in the 6months initiation. The frequency of UTI in the 6months post SGLT2 initiation was not significantly increased compared to the DPP-4 cohort (3.6%vs 4.9%; aHR=0.90, 95% CI 0.66-1.24). Genital infection were more frequent in the SGLT2 than in the DPP-4 cohort (2.9% vs 0.9%, aHR=3.50, 95% CI 1.95-5.89).
Conclusions: Similar to existing evidence, we found a higher risk of genital infection associated with SGLT2 inhibitors (primarily dapagliflozin) but no increased risk of UTIs compared to DPP-4 use.
SGLT2 inhibitors reduce the risk of renal failure in CKD stage 5 patients with Type 2 DM.
Huang B, Yen C, Wu C, Tsai C, Chen J, Hsiao C Sci Rep. 2025; 15(1):5872.
PMID: 39966427 PMC: 11836049. DOI: 10.1038/s41598-024-81973-z.
Sodium glucose cotransporter-2 inhibitors and heart disease: Current perspectives.
Mondal S, Pramanik S, Khare V, Fernandez C, Pappachan J World J Cardiol. 2024; 16(5):240-259.
PMID: 38817648 PMC: 11135334. DOI: 10.4330/wjc.v16.i5.240.
Park S, Jeong J, Woo Y, Choi Y, Shin S Sci Rep. 2023; 13(1):18462.
PMID: 37891260 PMC: 10611756. DOI: 10.1038/s41598-023-45793-x.
Alamro H, Bajic V, Macvanin M, Isenovic E, Gojobori T, Essack M Front Endocrinol (Lausanne). 2023; 13:1084656.
PMID: 36743910 PMC: 9893111. DOI: 10.3389/fendo.2022.1084656.
Shill M, Mohsin M, Showdagor U, Hasan S, Zahid M, Khan S Heliyon. 2023; 9(1):e12897.
PMID: 36685470 PMC: 9851879. DOI: 10.1016/j.heliyon.2023.e12897.