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Do obese children with diabetic ketoacidosis have type 1 or type 2 diabetes?
Joey C Low1, Eric I Felner, Andrew B Muir
1Department of Pediatrics, Division of Endocrinology, Emory University School of Medicine, 49 Jesse Hill Jr. Drive, Atlanta, GA 30303, USA.
Insights
Many obese children with diabetic ketoacidosis (DKA) show type 2 diabetes signs. Metformin improved glycemic control and remission rates in obese children with DKA, though remission was often temporary.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Diabetes Mellitus
Background:
- Diabetic ketoacidosis (DKA) in obese children often presents with type 2 diabetes characteristics.
- Understanding the long-term course and autoimmune markers in DKA is crucial for effective management.
Purpose of the Study:
- To describe the clinical presentation, autoimmune markers, and long-term outcomes of obese versus lean children with DKA.
- To evaluate the impact of metformin on glycemic control and remission in obese children with DKA.
Main Methods:
- Retrospective review of medical records for obese and lean children diagnosed with unprovoked DKA.
- Analysis of clinical presentation, autoimmune markers, treatment interventions, and follow-up outcomes.
Main Results:
- Obese children with DKA were older, predominantly male, and had fewer autoantibodies compared to lean children.
- Half of obese children achieved near-normoglycemia remission, unlike lean children. Metformin improved glycemic control, remission rates, and reduced DKA recurrence.
- Remission in obese children was often short-lived, with many requiring insulin reinitiation within 15 months.
Conclusions:
- Obese children with DKA exhibit features of type 2 diabetes, differing from lean counterparts.
- Metformin addition to insulin therapy in obese children with DKA enhances glycemic control, remission rates, and prevents recurrence.
- Despite improvements, long-term insulin independence remains a challenge for many obese children post-DKA.
Objective:
Many obese children with unprovoked diabetic ketoacidosis (DKA) display clinical features of type 2 diabetes during follow up. We describe the clinical presentation, autoimmune markers and the long-term course of obese and lean children with DKA.
Research Design And Methods:
We reviewed the medical records on the initial acute hospitalization and outpatient follow-up care of 21 newly diagnosed obese and 20 lean children with unprovoked DKA at Emory University affiliated children's hospitals between 1/2003 and 12/2006.
Results:
Obese children with DKA were older and predominantly male, had acanthosis nigricans, and had lower prevalence of autoantibodies to islet cells and glutamic acid decarboxylase than lean children. Half of the obese, but none of the lean children with DKA achieve near-normoglycemia remission and discontinued insulin therapy during follow-up. Time to achieve remission was 2.2±2.3 months. There were no differences on clinical presentation between obese children who achieved near-normoglycemia remission versus those who did not. The addition of metformin to insulin therapy shortly after resolution of DKA resulted in lower hemoglobin A1c (HbA1c) levels, higher rates of near-normoglycemia remission, and lower frequency of DKA recurrence. Near-normoglycemia remission, however, was of short duration and the majority of obese patients required reinstitution of insulin treatment within 15 months of follow-up.
Conclusion:
In contrast to lean children with DKA, many obese children with unprovoked DKA display clinical and immunologic features of type 2 diabetes during follow-up. The addition of metformin to insulin therapy shortly after resolution of DKA improves glycemic control, facilitates achieving near-normoglycemia remission and prevents DKA recurrence in obese children with DKA.
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