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Effects of Sustained Treatment With Lixisenatide on Gastric Emptying and Postprandial Glucose Metabolism in Type 2 Diabetes: A Randomized Controlled Trial.

Authors :
Rayner, Christopher K.
Watson, Linda E.
Phillips, Liza K.
Lange, Kylie
Bound, Michelle J.
Grivell, Jacqueline
Wu, Tongzhi
Jones, Karen L.
Horowitz, Michael
Ferrannini, Ele
Tricò, Domenico
Frascerra, Silvia
Mari, Andrea
Natali, Andrea
Source :
Diabetes Care. Aug2020, Vol. 43 Issue 8, p1813-1821. 9p.
Publication Year :
2020

Abstract

<bold>Objective: </bold>Tachyphylaxis for slowing of gastric emptying is seen with continuous exposure to glucagon-like peptide 1 (GLP-1). We therefore aimed to establish whether prolonged use of a "short-acting" GLP-1 receptor agonist, lixisenatide, achieves sustained slowing of gastric emptying and reduction in postprandial glycemia.<bold>Research Design and Methods: </bold>A total of 30 patients with metformin-treated type 2 diabetes underwent assessment of gastric emptying (scintigraphy) and glucose metabolism (dual tracer technique) after a 75-g glucose drink, before and after 8 weeks' treatment with lixisenatide (20 μg subcutaneously daily) or placebo, in a double-blind randomized parallel design.<bold>Results: </bold>Gastric retention of the glucose drink was markedly increased after lixisenatide versus placebo (ratio of adjusted geometric means for area under the curve [AUC] over 240 min of 2.19 [95% CI 1.82, 2.64], P < 0.001), associated with substantial reductions in the rate of systemic appearance of oral glucose (P < 0.001) and incremental AUC for blood glucose (P < 0.001). Lixisenatide suppressed both glucagon (P = 0.003) and insulin (P = 0.032), but not endogenous glucose production, over 120 min after oral glucose intake. Postprandial glucose lowering over 240 min was strongly related to the magnitude of slowing of gastric emptying by lixisenatide (r = -0.74, P = 0.002) and to the baseline rate of emptying (r = 0.52, P = 0.048) but unrelated to β-cell function (assessed by β-cell glucose sensitivity).<bold>Conclusions: </bold>Eight weeks' treatment with lixisenatide is associated with sustained slowing of gastric emptying and marked reductions in postprandial glycemia and appearance of ingested glucose. Short-acting GLP-1 receptor agonists therefore potentially represent an effective long-term therapy for specifically targeting postprandial glucose excursions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01495992
Volume :
43
Issue :
8
Database :
Academic Search Index
Journal :
Diabetes Care
Publication Type :
Academic Journal
Accession number :
144653720
Full Text :
https://doi.org/10.2337/dc20-0190