Treatment of an Opposing Metabolic Situation: GLUT1‐Deficiency Syndrome and Type 1 Diabetes
Anna K. Schoenlaub, Alexander Hoeller, Sabine Hofer, Edda Haberlandt, Elisabeth Steichen‐Gersdorf, Daniela Karall, Dorottya Forster, Sabine Scholl‐Bürgi

TL;DR
A 15-year-old girl with a rare brain metabolism disorder was successfully treated with a ketogenic diet, but later developed type 1 diabetes, which was managed alongside the diet.
Contribution
This case demonstrates the feasibility of managing both GLUT1-DS and type 1 diabetes with a modified ketogenic diet and insulin therapy.
Findings
The patient remained stable on a modified Atkins diet and insulin pump therapy for 2 years with no further DKA episodes.
HbA1c levels were maintained at 6.9% while on the combined treatment regimen.
Careful monitoring of blood glucose and β-hydroxybutyrate levels is essential for successful management.
Abstract
Glucose transporter type 1 deficiency syndrome (GLUT1‐DS) is a rare inborn disorder of metabolism leading to encephalopathy due to disturbed glucose transport via the blood–brain‐barrier and consecutive energy deficit of the brain. Since ketone bodies can serve as an alternative fuel for the brain, ketogenic diet therapies (KDT) are the treatment of choice for these patients. KDT refers to all forms of nutrition that lead to the formation of ketone bodies. We describe a 15‐year‐old girl with GLUT1‐DS who was effectively treated with a form of KDT, a modified Atkins diet (MAD), and developed type 1 diabetes. After correction of the initial diabetic ketoacidosis (DKA), insulin pump treatment was started while staying on MAD. With this treatment regimen, no further DKA episodes occurred within 2 years of follow‐up, current HbA1c 6.9%. Treatment of GLUT1‐DS by KDT and type 1 diabetes (T1D)…
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Taxonomy
TopicsDiet and metabolism studies · Diet, Metabolism, and Disease · Metabolism and Genetic Disorders
