Reduced Postprandial Concentrations of Intact Biologically Active Glucagon-Like Peptide 1 in Type 2 Diabetic Patients

• Published in: Diabetes (New York, N.Y.) Vol. 50; no. 3; pp. 609 - 613
• Main Authors: Vilsbøll, Tina, Krarup, Thure, Deacon, Carolyn F., Madsbad, Sten, Holst, Jens J.
• Format: Journal Article
• Language: English
• Published: Alexandria, VA American Diabetes Association 01.03.2001
• Subjects: Aged; Biological and medical sciences; C-Peptide - blood; Care and treatment; Diabetes; Diabetes Mellitus, Type 2 - blood; Diabetes. Impaired glucose tolerance; Diabetics; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Enzymes; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Evaluation; Fasting - blood; Female; Gastric Inhibitory Polypeptide - blood; Glucagon; Glucagon - blood; Glucagon - chemistry; Glucagon-Like Peptide 1; Glucose; Hormones; Humans; Insulin; Insulin - blood; Male; Medical sciences; Metabolites; Middle Aged; Osmolar Concentration; Peptide Fragments - blood; Peptide Fragments - chemistry; Peptides; Plasma; Polypeptides; Postprandial Period; Protein Precursors - blood; Protein Precursors - chemistry; Reference Values; Type 2 diabetes; United States; Endocrinopathy; Human; Body mass index; Gastrointestinal hormone; Postprandial; Sex; Gastric inhibitory peptide; Non insulin dependent diabetes; Age; Glucagon like peptide 1
• ISSN: 0012-1797; 1939-327X
• DOI: 10.2337/diabetes.50.3.609

Reduced Postprandial Concentrations of Intact Biologically Active Glucagon-Like Peptide 1 in Type 2 Diabetic Patients Tina Vilsbøll 1 2 , Thure Krarup 1 , Carolyn F. Deacon 2 , Sten Madsbad 3 and Jens J. Holst 2 1 Department of Internal Medicine F, Gentofte Hospital 2 Department of Medical Physiology, the Panum Institute 3 Department of Endocrinology, Hvidovre Hospital, University of Copenhagen, Copenhagen, Denmark Abstract Incretin hormones importantly enhance postprandial insulin secretion but are rapidly degraded to inactive metabolites by ubiquitous dipeptidyl peptidase IV. The concentrations of the intact biologically active hormones remain largely unknown. Using newly developed assays for intact glucagon-like peptide (GLP)-1 and glucose-dependent insulinotropic polypeptide (GIP), we measured plasma concentrations after a mixed breakfast meal (566 kcal) in 12 type 2 diabetic patients (age 57 years [range 49–67], BMI 31 kg/m 2 [27–38], and HbA 1c 9.2% [7.0–12.5]) and 12 matched healthy subjects. The patients had fasting hyperglycemia (10.7 mmol/l [8.0–14.8]) increasing to 14.6 mmol/l (11.5–21.5) 75 min after meal ingestion. Fasting levels of insulin and C-peptide were similar to those of the healthy subjects, but the postprandial responses were reduced and delayed. Fasting levels and meal responses were similar between patients and healthy subjects for total GIP (intact + metabolite) as well as intact GIP, except for a small decrease in the patients at 120 min; integrated areas for intact hormone (area under the curve [AUC] INT ) averaged 52 ± 4% (for patients) versus 56 ± 3% (for control subjects) of total hormone AUC (AUC TOT ). AUC INT for GLP-1 averaged 48 ± 2% (for patients) versus 51 ± 5% (for control subjects) of AUC TOT . AUC TOT for GLP-1 as well as AUC INT tended to be reduced in the patients ( P = 0.2 and 0.07, respectively); but the profile of the intact GLP-1 response was characterized by a small early rise (30–45 min) and a significantly reduced late phase (75–150 min) ( P < 0.02). The measurement of intact incretin hormones revealed that total as well as intact GIP responses were minimally decreased in patients with type 2 diabetes, whereas the late intact GLP-1 response was strongly reduced, supporting the hypothesis that an impaired function of GLP-1 as a transmitter in the enteroinsular axis contributes to the inappropriate insulin secretion in type 2 diabetes. AUC, area under the curve DPP-IV, dipeptidyl peptidase IV GIP, glucose-dependent insulinotropic polypeptide GLP, glucagon-like peptide RIA, radioimmunoassay Footnotes Address correspondence and reprint requests to Jens Juul Holst, MD, Professor of Medical Physiology, Department of Medical Physiology, The Panum Institute, DK-2200 Copenhagen N, Denmark. E-mail: holst{at}mfi.ku.dk . Received for publication 27 June 2000 and accepted in revised form 15 November 2000.