Sodium‐glucose co‐transporter‐2 inhibitors and diabetic ketoacidosis: A n updated review of the literature
Abstract
Sodium-glucose cotransporter-2 inhibitors (SGLT2is) are increasingly used for the treatment of type 2 diabetes (T2D) and can improve glucose control also in type 1 diabetes (T1D). In May 2015, regulatory agencies issued a warning that SGLT2is may cause diabetic ketoacidosis (DKA). We report details on 2 new cases of SGLT2i-associated DKA and review the literature for similar cases within randomized controlled trials (RCTs), cohort studies and single reports. We searched the medical literature for reports of SGLT2i-associated DKA cases. A quantitative analysis of frequency and clinical characteristics is reported. The 2 narrative cases illustrate that SGLT2i-associated DKA can occur in patients with T1D incorrectly diagnosed as T2D, perhaps without the presence of obvious DKA precipitating factors. The incidence of SGLT2i-associated DKA was less than 1/1000 in randomized controlled trials and 1.6/1000 person-years in cohort studies. We retrieved detailed data on 105 SGLT2i-associated DKA case reports, wherein 35% showed glucose levels of less than 200 mg/dL and 22% were not associated with typical triggers. In case reports and in pharmacovigilance databases, duration of SGLT2i treatment before DKA onset was extremely variable. Fatal SGLT2i-associated DKA episodes were found only in pharmacovigilance databases and represented 1.6% of all reported cases. DKA is a rare adverse event during SGLT2i therapy. Predisposing and precipitating factors are still incompletely understood, a…
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Up to a third of people treated with SGLT2 inhibitors who developed DKA present with glucose levels <200 mg/dL.
“Up to a third of people treated with SGLT2 inhibitors who developed DKA present with glucose levels <200 mg/dL (11.1 mmol/L) (239), and in one study 71% presented with glucose levels #250 mg/dL (13.9 mmol/L) (240)”
From 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes—2025 (2025) · cites this paper as [239]
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- Authors
- Bonora, B. M., Avogaro, A., & Fadini, G. P.
- Affiliations
- University of Padua (IT)
- Corresponding author
- Fadini, Gian Paolo
- Venue
- Diabetes, Obesity and Metabolism
- Publisher
- Wiley
- Published
- 2017-07-06
- Volume
- 20
- Issue
- 1
- Pages
- 25-33
- ISSN
- 1462-8902 (ISSN-L)
- 1463-1326
- OpenAlex
- W2615244338
- Cited by
- 118
- References
- 66
- Citations by year
- 2026: 6 · 2025: 19 · 2024: 12 · 2023: 12 · 2022: 10 · 2021: 13 · 2020: 18 · 2019: 16 · 2018: 11 · 2017: 1
- FWCI
- 1.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes Obesity and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Padua Research Archive (University of Padova) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
- Keywords
- SGLT2 inhibitors, diabetic ketoacidosis, type 1 diabetes misdiagnosis, adverse drug reactions, pharmacovigilance, drug safety, type 2 diabetes
- MeSH terms
- Sodium-Glucose Transporter 2 Inhibitors, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Diagnostic Errors, Humans, Hyperglycemia, Hypoglycemia, Hypoglycemic Agents, Diabetic Ketoacidosis, Membrane Transport Modulators, Sodium-Glucose Transporter 2, Pharmacovigilance
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