Efficacy of imeglimin in patients with type 2 diabetes mellitus complicated by metabolic dysfunction‐associated steatotic liver disease: A multicentre study

医学 瞬态弹性成像 内科学 胃肠病学 背景(考古学) 2型糖尿病 糖尿病 肝功能 脂肪肝 纤维化 肝病 代谢综合征 肝纤维化 疾病 内分泌学 古生物学 生物
作者
Kensaku Fukunaga,Asahiro Morishita,Hitomi Imachi,Kyoko Oura,Seisuke Sato,Toshihiro Kobayashi,Takanobu Saheki,Takafumi Yoshimura,K. Komori,Mai Nakahara,Tomoko Tadokoro,Koji Fujita,Joji Tani,Hideki Kobara,Koji Murao
出处
期刊:Diabetes, Obesity and Metabolism [Wiley]
被引量:1
标识
DOI:10.1111/dom.16157
摘要

Abstract Aims This study aimed to evaluate the effectiveness of imeglimin in improving liver function and fibrosis in patients with type 2 diabetes (T2D) complicated by metabolic dysfunction‐associated steatotic liver disease (MASLD). Materials and Methods We conducted a multicentre study involving 80 patients with T2D and MASLD who were treated with or without imeglimin for 24 weeks. We assessed the changes in diabetes‐related parameters, including HbA1c, fasting blood glucose, glycoalbumin and C‐peptide index. Liver function was monitored using AST, ALT, γ‐GTP and liver fibrosis indicators such as Fib‐4 index and FibroScan‐AST (FAST) score. Liver fat content and stiffness were measured using controlled attenuation parameter and vibration‐controlled transient elastography, which were measured using FibroScan. Results Compared with the control group, imeglimin treatment led to a significant reduction in HbA1c levels, fasting blood glucose and liver‐related parameters, including AST, ALT and γ‐GTP. Additionally, the Fib‐4 index and FAST score, which reflect liver fibrosis and inflammation, were significantly lower in the imeglimin group. Liver fat content and stiffness remained unchanged during the study period. Conclusions Imeglimin efficaciously improved liver inflammation and fibrosis in patients with T2D and MASLD, with no significant changes in liver fat content or stiffness. These findings suggest that imeglimin is a promising therapeutic drug for the management of MASLD in the context of T2D, warranting further research on its long‐term efficacy and mechanisms of action.

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