TY - JOUR
T1 - Effect of the incretin hormones on the endocrine pancreas in end-stage renal disease
AU - Jørgensen, Morten B
AU - Idorn, Thomas
AU - Rydahl, Casper
AU - Hansen, Henrik P
AU - Bressendorff, Iain
AU - Brandi, Lisbet
AU - Wewer Albrechtsen, Nicolai J
AU - van Hall, Gerrit
AU - Hartmann, Bolette
AU - Holst, Jens J
AU - Knop, Filip K
AU - Hornum, Mads
AU - Feldt-Rasmussen, Bo
N1 - © Endocrine Society 2019. All rights reserved. For permissions, please e-mail: [email protected].
PY - 2020/3
Y1 - 2020/3
N2 - Context: The insulin-stimulating and glucagon-regulating effects of the 2 incretin hormones, glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), contribute to maintain normal glucose homeostasis. Impaired glucose tolerance occurs with high prevalence among patients with end-stage renal disease (ESRD). Objective: To evaluate the effect of the incretin hormones on endocrine pancreatic function in patients with ESRD. Design and Setting: Twelve ESRD patients on chronic hemodialysis and 12 matched healthy controls, all with normal oral glucose tolerance test, were included. On 3 separate days, a 2-hour euglycemic clamp followed by a 2-hour hyperglycemic clamp (3 mM above fasting level) was performed with concomitant infusion of GLP-1 (1 pmol/kg/min), GIP (2 pmol/kg/min), or saline administered in a randomized, double-blinded fashion. A 30% lower infusion rate was used in the ESRD group to obtain comparable incretin hormone plasma levels. Results: During clamps, comparable plasma glucose and intact incretin hormone concentrations were achieved. The effect of GLP-1 to increase insulin concentrations relative to placebo levels tended to be lower during euglycemia in ESRD and was significantly reduced during hyperglycemia (50 [8-72]%, P = 0.03). Similarly, the effect of GIP relative to placebo levels tended to be lower during euglycemia in ESRD and was significantly reduced during hyperglycemia (34 [13-50]%, P = 0.005). Glucagon was suppressed in both groups, with controls reaching lower concentrations than ESRD patients. Conclusions: The effect of incretin hormones to increase insulin release is reduced in ESRD, which, together with elevated glucagon levels, could contribute to the high prevalence of impaired glucose tolerance among ESRD patients.
AB - Context: The insulin-stimulating and glucagon-regulating effects of the 2 incretin hormones, glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), contribute to maintain normal glucose homeostasis. Impaired glucose tolerance occurs with high prevalence among patients with end-stage renal disease (ESRD). Objective: To evaluate the effect of the incretin hormones on endocrine pancreatic function in patients with ESRD. Design and Setting: Twelve ESRD patients on chronic hemodialysis and 12 matched healthy controls, all with normal oral glucose tolerance test, were included. On 3 separate days, a 2-hour euglycemic clamp followed by a 2-hour hyperglycemic clamp (3 mM above fasting level) was performed with concomitant infusion of GLP-1 (1 pmol/kg/min), GIP (2 pmol/kg/min), or saline administered in a randomized, double-blinded fashion. A 30% lower infusion rate was used in the ESRD group to obtain comparable incretin hormone plasma levels. Results: During clamps, comparable plasma glucose and intact incretin hormone concentrations were achieved. The effect of GLP-1 to increase insulin concentrations relative to placebo levels tended to be lower during euglycemia in ESRD and was significantly reduced during hyperglycemia (50 [8-72]%, P = 0.03). Similarly, the effect of GIP relative to placebo levels tended to be lower during euglycemia in ESRD and was significantly reduced during hyperglycemia (34 [13-50]%, P = 0.005). Glucagon was suppressed in both groups, with controls reaching lower concentrations than ESRD patients. Conclusions: The effect of incretin hormones to increase insulin release is reduced in ESRD, which, together with elevated glucagon levels, could contribute to the high prevalence of impaired glucose tolerance among ESRD patients.
KW - Adult
KW - Denmark
KW - Double-Blind Method
KW - Female
KW - Glucagon-Like Peptide 1/administration & dosage
KW - Glucagon/blood
KW - Glucose Clamp Technique
KW - Glucose Tolerance Test
KW - Humans
KW - Incretins/administration & dosage
KW - Insulin Secretion/drug effects
KW - Insulin/metabolism
KW - Islets of Langerhans/drug effects
KW - Kidney Failure, Chronic/metabolism
KW - Male
KW - Middle Aged
KW - Renal Dialysis
UR - http://www.scopus.com/inward/record.url?scp=85077666349&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgz048
DO - 10.1210/clinem/dgz048
M3 - Journal article
C2 - 31608934
SN - 0021-972X
VL - 105
SP - E564-E574
JO - The Journal of clinical endocrinology and metabolism
JF - The Journal of clinical endocrinology and metabolism
IS - 3
M1 - dgz048
ER -