Too much glucagon, too little insulin: time course of pancreatic islet dysfunction in new-onset type 1 diabetes

Diabetes Care. 2008 Jul;31(7):1403-4. doi: 10.2337/dc08-0575.

Abstract

Objective: To determine the time course of changes in glucagon and insulin secretion in children with recently diagnosed type 1 diabetes.

Research design and methods: Glucagon and C-peptide concentrations were determined in response to standard mixed meals in 23 patients with type 1 diabetes aged 9.4 +/- 4.6 years, beginning within 6 weeks of diagnosis, and every 3 months thereafter for 1 year.

Results: Glucagon secretion in response to a physiologic stimulus (mixed meal) increased by 37% over 12 months, while C-peptide secretion declined by 45%. Fasting glucagon concentrations remained within the normal (nondiabetic) reference range.

Conclusions: Postprandial hyperglucagonemia worsens significantly during the first year after diagnosis of type 1 diabetes and may represent a distinct therapeutic target. Fasting glucagon values may underestimate the severity of hyperglucagonemia. The opposing directions of abnormal glucagon and C-peptide secretion over time support the link between dysregulated glucagon secretion and declining beta-cell function.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adolescent
  • Age of Onset
  • C-Peptide / blood
  • Child
  • Child, Preschool
  • Diabetes Mellitus, Type 1 / blood*
  • Eating
  • Fasting
  • Female
  • Follow-Up Studies
  • Glucagon / blood*
  • Glucagon / metabolism
  • Humans
  • Insulin / blood*
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / physiopathology*
  • Male

Substances

  • C-Peptide
  • Insulin
  • Glucagon