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Updated: Dec 11, 2025

Homogeneous Time-resolved Förster Resonance Energy Transfer-based Assay for Detection of Insulin Secretion
Published on: May 10, 2018
[SGLT 2 inhibitors in Type 1 diabetes]
Elisabeth Buur Stougaard1, Hanan Amadid, Esben Søndergaard
1elisabeth.buur.stougaard@regionh.dk.
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) like dapagliflozin aid Type 1 diabetes management but increase diabetic ketoacidosis (DKA) risk. Importantly, SGLT2i-associated DKA can occur with normal blood sugar levels.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are approved for Type 1 diabetes (T1D) treatment.
- Dapagliflozin, an SGLT2i, shows benefits like reduced HbA1c, weight, and insulin dose, with increased time in range.
- A notable side effect is an increased risk of diabetic ketoacidosis (DKA).
Purpose of the Study:
- To review the risk and presentation of diabetic ketoacidosis (DKA) in Type 1 diabetes (T1D) patients treated with SGLT2 inhibitors.
- To highlight the potential for euglycaemic DKA in this patient population.
Main Methods:
- Literature review focusing on SGLT2 inhibitor use in T1D.
- Analysis of studies reporting DKA events in T1D patients on SGLT2 inhibitors.
- Examination of DKA presentation, including blood glucose levels.
Main Results:
- SGLT2 inhibitor use in T1D is associated with a significant increase in DKA risk, from 1.9% to 4.0%.
- Diabetic ketoacidosis (DKA) in patients on SGLT2 inhibitors can present with normal or near-normal blood glucose levels (euglycaemic DKA).
Conclusions:
- Physicians must be aware that DKA can manifest with normal glycemia in T1D patients using SGLT2 inhibitors.
- Vigilance for euglycaemic DKA is crucial for timely diagnosis and management in T1D patients on SGLT2i therapy.
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