# The Involvement of Apoptosis Inhibitor of Macrophage in the Disease Severity of Primary Biliary Cholangitis

**Authors:** Takashi Himoto, Erika Mori, Manami Tanimoto, Koji Fujita, Shima Mimura, Tomoko Tadokoro, Kyoko Oura, Joji Tani, Asahiro Morishita, Hideki Kobara

PMC · DOI: 10.3390/jcm15031169 · Journal of Clinical Medicine · 2026-02-02

## TL;DR

This study explores the role of a protein called AIM in a liver disease called primary biliary cholangitis and finds it may not be linked to obesity or diabetes but could be related to disease severity.

## Contribution

The study investigates the role of AIM in primary biliary cholangitis, revealing its potential association with disease severity but not with obesity or insulin resistance.

## Key findings

- AIM levels in PBC patients were not associated with obesity or T2DM.
- AIM levels were significantly influenced by immunoglobulin G, albumin, tumor necrosis factor-α, and histological stages.
- Patients with T2DM had higher ALT levels and more advanced liver disease stages.

## Abstract

Background: A protein called ‘apoptosis inhibitor of macrophage (AIM)’ is involved in the pathogenesis of obesity-associated disease. Although it is widely recognized that concurrent obesity affects the disease progression of chronic liver disease, as does concurrent type 2 diabetes mellitus (T2DM), the involvement of AIM in the pathogenesis of obesity or insulin resistance is not yet understood in patients with primary biliary cholangitis (PBC). Methods: Obesity was defined as a body mass index (BMI) exceeding 25, and insulin resistance was defined as a homeostasis model assessment for insulin resistance (HOMA-IR) value exceeding 2.0, respectively. Hepatic steatosis was estimated based on the classification proposed by Brunt and colleagues. The histological stage was determined by Scheuer’s classification. Results: Twelve (25.0%) of the forty-eight PBC patients had concurrent obesity, and seven (14.6%) had concurrent T2DM. The PBC patients with obesity had significantly higher frequency of hepatic steatosis. Compared to the patients without T2DM, those with concurrent T2DM had significantly higher serum ALT levels and more advanced histological stages. The patients’ serum AIM levels were not associated with concurrent obesity or concurrent T2DM. Our analyses identified the following as the factors that significantly affected the patients’ AIM levels: serum immunoglobulin G, albumin, tumor necrosis factor-α levels, and the histological stages. Conclusions: These results indicate that AIM may not be involved in obesity or insulin resistance, but it may be associated with the disease severity of PBC.

## Linked entities

- **Diseases:** primary biliary cholangitis (MONDO:0005388), obesity (MONDO:0011122), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** CD5L (CD5 molecule like) [NCBI Gene 922] {aka AIM, API6, CT-2, PRO229, SP-ALPHA, Spalpha}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** chronic liver disease (MESH:D008107), insulin resistance (MESH:D007333), Hepatic steatosis (MESH:D005234), PBC (MESH:D008105), Obesity (MESH:D009765), T2DM (MESH:D003924)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897933/full.md

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Source: https://tomesphere.com/paper/PMC12897933