Imeglimin increases glucose‐dependent insulin secretion and improves β‐cell function in patients with type 2 diabetes. Issue 6 (25th March 2015)

• Record Type: Journal Article
• Authors: Pacini, G.; Mari, A.; Fouqueray, P.; Bolze, S.; Roden, M.
• Is Part Of: Diabetes, obesity & metabolism. Volume 17:Issue 6(2015:Jun.)
• Page Start: 541
• Page End: 545
• Publication Date: 2015-03-25
• Subjects: Diabetes -- Periodicals; Obesity -- Periodicals; Metabolism -- Disorders -- Periodicals; Clinical pharmacology -- Periodicals; 616.462
• DOI: 10.1111/dom.12452
• Languages: English
• ISSNs: 1462-8902

Abstract

<abstract abstract-type="main" id="dom12452-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="dom12452-sec-0001" sec-type="section"> <title>Aims</title> <p id="dom12452-para-0001">To assess the glucose‐stimulated insulin secretion effect of imeglimin in patients with type 2 diabetes.</p> </sec> <sec id="dom12452-sec-0002" sec-type="section"> <title>Methods</title> <p id="dom12452-para-0002">We conducted a double‐blind, randomized, placebo‐controlled study in 33 patients with type 2 diabetes [glycated haemoglobin 6.8 ± 0.1% (51 mmol/mol)], who were drug‐naïve or withdrawn from their previous metformin monotherapy for 2 weeks and received imeglimin 1500 mg twice daily or placebo for 1 week. Glucose‐stimulated insulin secretion was assessed using a hyperglycaemic clamp. The primary endpoint was insulin secretion as defined by total insulin response [incremental area under the curve (iAUC)<sub>0–45 min</sub>] and insulin secretion rate (ISR) calculated from C‐peptide deconvolution. β‐cell glucose sensitivity at steady state (second phase: 25–45 min), hepatic insulin extraction and insulin clearance were also calculated.</p> </sec> <sec id="dom12452-sec-0003" sec-type="section"> <title>Results</title> <p id="dom12452-para-0003">Imeglimin treatment for 7 days raised the insulin secretory response to glucose by +112% (iAUC<sub>0‐45</sub>, p = 0.035), first‐phase ISR by +110% (p = 0.034) and second‐phase ISR by +29% (p = 0.031). Imeglimin improved β‐cell glucose sensitivity by +36% (p = 0.034) and tended to decrease hepatic insulin extraction (−13%; p = 0.056). Imeglimin did not affect glucagon secretion.</p> </sec> <sec id="dom12452-sec-0004" sec-type="section"> <title>Conclusions</title> <p id="dom12452-para-0004">In patients with type 2 diabetes, imeglimin improves β‐cell function, which may contribute to the glucose‐lowering effect observed with imeglimin in clinical trials.</p> </sec> </abstract>