Diabetes in a Patient with Glycogen Storage Disease Type 1a

Intern Med. 2024 Aug 1;63(15):2153-2156. doi: 10.2169/internalmedicine.2766-23. Epub 2024 Jan 2.

Abstract

Glycogen storage disease type 1a (GSD-1a) is a rare congenital disease. Recently, life expectancy with GSD-1a has been improved by its early diagnosis and management. Complications of diabetes with GSD-1a are extremely rare. The optimal treatment for glucose control using this disease combination remains unclear. The existence of GSD-1a and diabetes can cause both hypoglycemia and hyperglycemia, making glucose control especially problematic. In the present report, α-glucosidase inhibitor (α-GI) and dipeptidyl peptidase-4 (DPP-4) inhibitors improved hyperglycemia without symptoms of hypoglycemia in a patient with diabetes and GSD-1a using intermittent continuous glucose monitoring (isCGM).

Keywords: diabetes; dipeptidyl peptidase-4 inhibitor; glycogen storage disease type 1a; hypoglycemia; intermittently scanned continuous glucose monitoring; α-glucosidase inhibitor.

Publication types

  • Case Reports

MeSH terms

  • Blood Glucose / metabolism
  • Dipeptidyl-Peptidase IV Inhibitors / therapeutic use
  • Glycogen Storage Disease Type I* / complications
  • Glycogen Storage Disease Type I* / diagnosis
  • Glycoside Hydrolase Inhibitors* / therapeutic use
  • Humans
  • Hyperglycemia / complications
  • Hyperglycemia / diagnosis
  • Hypoglycemic Agents / therapeutic use

Substances

  • Blood Glucose
  • Dipeptidyl-Peptidase IV Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Hypoglycemic Agents