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Imeglimin for Type 2 Diabetes Mellitus: Its Efficacy and Insight Into the Potential Benefit for Renal and Liver Function

Overview
Journal Cureus
Date 2024 Sep 6
PMID 39238763
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Abstract

Introduction Imeglimin is a novel oral antihyperglycaemic drug used to treat type 2 diabetes mellitus (T2DM). In 2022, its clinical use was approved in Japan; however, there is limited data on its practical efficacy. Thus, we retrospectively investigated the clinical efficacy of imeglimin for six months at the National Defense Medical College, Tokorozawa, Japan. Material and methods We conducted a single-center retrospective analysis to elucidate the efficacy of imeglimin in the treatment of T2DM. Ten patients were enrolled, and their biomarkers and geographic data were analyzed. The primary endpoint was the change in HbA1c level at six months after imeglimin treatment compared to the baseline values. Other demographic and laboratory parameters, including sex, age, BMI, renal function, liver function, lipid profile, and transient elastography data, were also analyzed. Results A significant improvement in the HbA1c levels (8.1 % at baseline to 6.9 % at six months after treatment, P value = 0.01) was observed in this study, suggesting that imeglimin is a promising option for treating T2DM. In addition, no negative effects on renal function were observed, and albumin levels tended to decrease from baseline values. Among the nonalcoholic fatty liver disease (NAFLD) cases, liver conditions, especially fat content, tended to improve in this short-term period. Conclusions Imeglimin is suggested to have a beneficial effect not only on glycemic control but also on renal and liver function. However, further studies are required to better understand the long-term efficacy of this drug.

Citing Articles

A Multicenter, Retrospective Study to Evaluate the Effectiveness and Safety of Imeglimin in Patients with Type 2 Diabetes Mellitus in a Real-World Clinical Setting (INDI-TIMES Study).

Shaikh S, Sharma S, Phatak S, Asirvatham A, Bhattacharyya S, Dhandhania V Diabetes Ther. 2025; .

PMID: 39969754 DOI: 10.1007/s13300-025-01693-z.

References
1.
Vial G, Chauvin M, Bendridi N, Durand A, Meugnier E, Madec A . Imeglimin normalizes glucose tolerance and insulin sensitivity and improves mitochondrial function in liver of a high-fat, high-sucrose diet mice model. Diabetes. 2015; 64(6):2254-64. DOI: 10.2337/db14-1220. View

2.
Chalasani N, Wilson L, Kleiner D, Cummings O, Brunt E, Unalp A . Relationship of steatosis grade and zonal location to histological features of steatohepatitis in adult patients with non-alcoholic fatty liver disease. J Hepatol. 2008; 48(5):829-34. PMC: 2346454. DOI: 10.1016/j.jhep.2008.01.016. View

3.
Ruggenenti P, Cravedi P, Remuzzi G . The RAAS in the pathogenesis and treatment of diabetic nephropathy. Nat Rev Nephrol. 2010; 6(6):319-30. DOI: 10.1038/nrneph.2010.58. View

4.
Fukami K, Yamagishi S, Ueda S, Okuda S . Role of AGEs in diabetic nephropathy. Curr Pharm Des. 2008; 14(10):946-52. DOI: 10.2174/138161208784139710. View

5.
Sanyal A, Chalasani N, Kowdley K, McCullough A, Diehl A, Bass N . Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N Engl J Med. 2010; 362(18):1675-85. PMC: 2928471. DOI: 10.1056/NEJMoa0907929. View