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Sodium-Glucose Co-Transporter 2 Inhibitors and Severe Urinary Tract Infections: Real-World Meta-Analysis of Cohort Studies

  • Mohammed Aboukaoud
  • , Yocheved Morhi
  • , Ester Osher*
  • *Corresponding author for this work
  • Rambam Health Care Campus Israel
  • Tel Aviv University
  • Technion-Israel Institute of Technology
  • Tel Aviv Sourasky Medical Center

Research output: Contribution to journalReview articlepeer-review

5 Scopus citations

Abstract

Objective: There is limited knowledge about severe urinary tract infections associated with SGLT2i, despite this being the basis for the Food and Drug Administration (FDA) warning. We aim to provide real-world evidence to clarify this relationship further. Data source: A literature review was performed in PubMed and Embase for cohort studies published up to August 2024 using PICO-consistent terms. Study selection and data extraction: Cohort studies in English involving new users of SGLT2i that compare SGLT2i with glucagon-like receptor agonists (GLP-1RA), DPP4i, and other glucose-lowering medications and report severe urinary tract infection (UTI). Data synthesis: The random-effect model determined the odds ratio (OR) and 95% confidence interval (CI) for severe UTI. Subgroup analysis and meta-regression were used to identify sources of heterogeneity. In 11 cohort studies involving 679 617 individuals with type 2 diabetes mellitus and a median age of 64 (interquartile range [IQR] = 56-72) and 42% (IQR = 39%-51%) females, it was found that the use of SGLT2i was associated with a reduced risk of severe UTI compared with both composite glucose-lowering medications (OR = 0.73, 95% CI = 0.60-0.88) and DPP4i (OR = 0.48, 95% CI = 0.43-0.54). There was no significant difference in the risk compared with GLP-1RA (OR = 0.94, 95% CI = 0.78-1.14). Relevance to patient care and clinical practice: The lack of increased risk for severe UTI reassures physicians when assessing benefit-risk to continue SGLT2i after a severe UTI. This may enhance patient adherence and improve diabetes management. Furthermore, our findings show no significant risk increase in chronic kidney disease (CKD) patients who would benefit significantly from SGLT2i. Conclusion: SGLT2i does not appear to pose a greater risk of severe UTI than other oral glucose-lowering medications. This contributes to the existing literature on UTI, accounting for the event’s severity. However, more data are needed to assess the potential association between SGLT2i and life-threatening UTI events.

Original languageEnglish
Pages (from-to)891-903
Number of pages13
JournalAnnals of Pharmacotherapy
Volume59
Issue number10
DOIs
StatePublished - Oct 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • glucagon-like peptide-1 receptor agonists
  • glucose-lowering medications
  • pyelonephritis
  • sodium-glucose co-transporter 2
  • urinary tract infections
  • urosepsis

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