Verification of the Short-Term Impact of Imeglimin on Liver Fibrosis Markers Stratified by Liver Fibrosis Risk in Patients With Type 2 Diabetes
Takumi Tanaka, Takashi Kitao, Motohiro Kubori, Yoshio Komoda, Yukiko Mori, Takeshi Ibata

TL;DR
This study found that imeglimin reduces liver fibrosis markers more in patients with type 2 diabetes and higher initial fibrosis risk.
Contribution
The study shows imeglimin's short-term impact on liver fibrosis markers varies by baseline fibrosis risk in T2DM patients.
Findings
FIB-4 significantly decreased in patients with moderate to high baseline fibrosis risk.
APRI decreased significantly across all subgroups after imeglimin treatment.
Greater reductions in FIB-4 and APRI were observed in patients with higher initial FIB-4 levels.
Abstract
Objective This study aimed to evaluate the effects of imeglimin on Fibrosis-4 index (FIB-4) and aspartate aminotransferase to platelet ratio index (APRI) across three subgroups classified according to the FIB-4 classification for assessing liver fibrosis risk in patients with type 2 diabetes mellitus (T2DM). Materials and methods Eighty-three patients with T2DM were classified into three subgroups based on their FIB-4 at the initiation of imeglimin, following the FIB-4 classification: Group 1 (G1) (FIB-4 < 1.30, n = 25), Group 2 (G2) (1.30 ≤ FIB-4 < 2.67, n = 44), and Group 3 (G3) (FIB-4 ≥ 2.67, n = 14). Then we evaluated the changes (Δ) in FIB-4 and APRI three months after the initiation of imeglimin in each subgroup. Subsequently, ΔFIB-4 and ΔAPRI were compared across the three subgroups. Baseline parameters and their changes correlated with ΔFIB-4 were also analyzed. Results…
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Taxonomy
TopicsLiver Disease Diagnosis and Treatment · Diet, Metabolism, and Disease · Pancreatic function and diabetes
