# Verification of the Short-Term Impact of Imeglimin on Liver Fibrosis Markers Stratified by Liver Fibrosis Risk in Patients With Type 2 Diabetes

**Authors:** Takumi Tanaka, Takashi Kitao, Motohiro Kubori, Yoshio Komoda, Yukiko Mori, Takeshi Ibata

PMC · DOI: 10.7759/cureus.82625 · 2025-04-20

## 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.

## Key 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

FIB-4 significantly decreased in G2 (p = 0.046) and G3 (p = 0.017), while APRI showed significant reductions across all three subgroups (G1: p = 0.007, G2: p < 0.001, G3: p = 0.002). ΔFIB-4 in G3 was significantly greater than that observed in G1 (p = 0.01), and ΔAPRI in G3 was significantly greater than those in G1 (p = 0.004) and G2 (p = 0.007). ΔFIB-4 was negatively correlated with baseline FIB-4 and Triglycerides (TG), and positively correlated with Δγ-glutamyl transpeptidase (γ-GTP).

Conclusions

The short-term effects of imeglimin on FIB-4 and APRI in patients with T2DM may be more pronounced in patients with higher baseline FIB-4 levels.

## Linked entities

- **Chemicals:** imeglimin (PubChem CID 24812808)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** MTG1 (mitochondrial ribosome associated GTPase 1) [NCBI Gene 92170] {aka GTP, GTPBP7}
- **Diseases:** T2DM (MESH:D003924), Liver Fibrosis (MESH:D008103), Fibrosis (MESH:D005355)
- **Chemicals:** TG (MESH:D014280), Imeglimin (MESH:C575881)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12091082/full.md

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Source: https://tomesphere.com/paper/PMC12091082