Related Experiment Video
Updated: Jul 4, 2025

Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test OGTT and Insulin Tolerance Test ITT
Published on: January 7, 2018
Sodium-Glucose Cotransporter-2 Inhibitor-Induced Euglycemic Diabetic Ketoacidosis in a Type 2 Diabetic Patient
Rakahn Haddadin1, Danny Aboujamra2, Homayon Iraninezhad3
1Medicine, MountainView Hospital, Las Vegas, USA.
Abstract:
Euglycemic diabetic ketoacidosis (euDKA) is a life-threatening metabolic complication typically associated with type 1 diabetes mellitus (T1DM). However, its occurrence in type 2 diabetes mellitus (T2DM) remains exceptionally rare. We present a case report detailing the unusual manifestation of euDKA in a patient with T2DM following the initiation of treatment with a sodium-glucose cotransporter-2 (SGLT-2) inhibitor. The patient, a 67-year-old female with a history of T2DM and well-controlled blood glucose levels, was commenced on an SGLT-2 inhibitor as part of her antidiabetic regimen just two weeks prior. Subsequently, the patient developed euDKA despite maintaining near-normal glycemic levels. This paradoxical presentation challenges the conventional understanding of DKA in T2DM and underscores the need for heightened clinical awareness. EuDKA associated with SGLT-2 inhibitors is an infrequently reported phenomenon, further complicating the clinical landscape. This case contributes to the growing evidence suggesting an association between SGLT-2 inhibitors and the development of euDKA in patients with T2DM. The rarity of this occurrence necessitates a thorough exploration of potential risk factors and underlying mechanisms.
Related Concept Videos
Diabetes Mellitus: Type 2 and Gestational
Oral Hypoglycemic Agents: Glinides
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Oral Hypoglycemic Agents: Biguanides and Glitazones
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
Dipeptidyl Peptidase 4 Inhibitors

