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Meal-Stimulated Glucagon Release Is Associated with Postprandial Blood Glucose Level and Does Not Interfere with Glycemic Control in Children and Adolescents with New-Onset Type 1 Diabetes

Pediatric Department (S.P., L.B.N., A.K., H.B.M.) and Department of Neurology (K.B.P.), Glostrup University Hospital, DK-2600 Glostrup, Denmark; Pediatric Clinic (M.K.), Department of Endocrinology and Genetics, 91000 Skopje, Republic of Macedonia; Clinica Pediatrica (F.C.), Ospedale Policlinico, 66013 Chieti, Italy; Medical Anatomy (C.Ø.) and Medical Physiology (J.J.H.), The Panum Institute, DK-2200 Copenhagen, Denmark; Statistics (P.H.), University of Southern Denmark, DK-5230 Odense, Denmark; and Development Projects (S.P., L.H.), Novo Nordisk A/S, DK-2880 Bagsværd, Denmark

Address all correspondence and requests for reprints to: Sven Pörksen, Department of Pediatrics, Forskerparken, Glostrup University Hospital, DK-2600 Glostrup, Denmark. E-mail: svepor01{at}glo.regionh.dk.

Context: The role of glucagon in hyperglycemia in type 1 diabetes is unresolved, and in vitro studies suggest that increasing blood glucose might stimulate glucagon secretion.

Objective: Our objective was to investigate the relationship between postprandial glucose and glucagon level during the first 12 months after diagnosis of childhood type 1 diabetes.

Design: We conducted a prospective, noninterventional, 12-month follow-up study conducted in 22 centers in 18 countries.

Patients: Patients included 257 children and adolescents less than 16 yr old with newly diagnosed type 1 diabetes; 204 completed the 12-month follow-up.

Setting: The study was conduced at pediatric outpatient clinics.

Main Outcome Measures: We assessed residual ß-cell function (C-peptide), glycosylated hemoglobin (HbA_1c), blood glucose, glucagon, and glucagon-like peptide-1 (GLP-1) release in response to a 90-min meal stimulation (Boost) at 1, 6, and 12 months after diagnosis.

Results: Compound symmetric repeated-measurements models including all three visits showed that postprandial glucagon increased by 17% during follow-up (P = 0.001). Glucagon levels were highly associated with postprandial blood glucose levels because a 10 mmol/liter increase in blood glucose corresponded to a 20% increase in glucagon release (P = 0.0003). Glucagon levels were also associated with GLP-1 release because a 10% increase in GLP-1 corresponded to a 2% increase in glucagon release (P = 0.0003). Glucagon levels were not associated (coefficient –0.21, P = 0.07) with HbA_1c, adjusted for insulin dose. Immunohistochemical staining confirmed the presence of Kir6.2/SUR1 in human -cells.

Conclusion: Our study supports the recent in vitro data showing a stimulation of glucagon secretion by high glucose levels. Postprandial glucagon levels were not associated with HbA_1c, adjusted for insulin dose, during the first year after onset of childhood type 1 diabetes.

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