Key result
The effect of GLP-1 and GIP to increase insulin concentrations during hyperglycemia was significantly reduced in ESRD patients by 50% (P=0.03) and 34% (P=0.005), respectively.
Why the study?
Impaired glucose tolerance is highly prevalent among patients with ESRD, but the effect of the incretin hormones GLP-1 and GIP on endocrine pancreatic function in ESRD was unknown.
Does infusion of incretin hormones (GLP-1 and GIP) increase insulin release in patients with ESRD compared to saline?
RCT (n=24)
Double-blind
randomized
Does infusion of incretin hormones (GLP-1 and GIP) increase insulin release in patients with ESRD compared to saline?
p-value: p=0.03 for GLP-1, 0.005 for GIP
The incretin effect on insulin release is reduced in ESRD, which may contribute to the high prevalence of impaired glucose tolerance in this population.
Reduced incretin insulinotropic effects in ESRD may underlie glucose intolerance; extends evidence of incretin resistance to advanced kidney disease.
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.
No takes yet. Share an insight, caveat, or question.
Jørgensen et al. (2019) conducted an RCT in End-stage renal disease (n=24). GLP-1 and GIP vs. Saline was evaluated on Insulin concentrations relative to placebo levels during hyperglycemia (p=0.03 for GLP-1, 0.005 for GIP). The effect of GLP-1 and GIP to increase insulin concentrations during hyperglycemia was significantly reduced in ESRD patients by 50% (P=0.03) and 34% (P=0.005), respectively.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: