# Clinical utility of the MAF-5 score for assessing MAFLD/MASLD in a Japanese population with obesity

**Authors:** Hayato Fukumitsu, Kazuhiko Sakaguchi, Marika Nishisaka, Yukari Katsura, Yasuko Morita, Natsu Otowa-Suematsu, Tomoko Yamada, Yoshihiko Yano, Michiko Takahashi, Shun-Ichiro Asahara, Wataru Ogawa

PMC · DOI: 10.1007/s13340-025-00874-2 · 2026-01-21

## TL;DR

The MAF-5 score is a useful noninvasive tool for predicting liver fibrosis in Japanese patients with MASLD, even among those with type 2 diabetes.

## Contribution

This study evaluates the MAF-5 score's clinical utility in Japanese MASLD patients, including those with diabetes, for the first time.

## Key findings

- The MAF-5 score significantly correlated with liver stiffness measurement (LSM) in Japanese MASLD patients.
- The MAF-5 score outperformed the FIB-4 index in predicting significant liver fibrosis.
- The MAF-5 score's predictive value was consistent regardless of diabetes status.

## Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) coexists with type 2 diabetes and is rising in Japan. Liver fibrosis progression in MASLD causes adverse outcomes, highlighting the need for early risk stratification. The utility of the Metabolic Dysfunction–Associated Fibrosis 5 (MAF-5) score has not been assessed in Japanese populations, especially among individuals with type 2 diabetes. Herein, the clinical relevance of the MAF-5 score was assessed in Japanese patients with MASLD.

This prespecified secondary analysis used data from a study titled “A Study to Estimate the Severity of MAFLD Using Continuous Glucose Monitoring.” Sixty-six patients diagnosed with metabolic dysfunction–associated fatty liver disease (MAFLD) underwent vibration-controlled transient elastography. All participants were subsequently confirmed to meet the revised diagnostic criteria for MASLD. The MAF-5 score and FIB-4 index were calculated for each participant. Correlations between these scores and liver stiffness measurement (LSM) were assessed using Spearman’s rank correlation coefficient. Significant fibrosis was defined as LSM ≥ 8.0 kPa. The predictive performance of each score was evaluated using the area under the receiver operating characteristic curve (AUROC).

The final analysis included 57 participants (28 with type 2 diabetes). The MAF-5 score significantly correlated with LSM, whereas the FIB-4 index did not. These associations were consistent regardless of diabetes status. The AUROC for the MAF-5 score was higher than that for the FIB-4 index.

The MAF-5 score may serve as a useful noninvasive marker for predicting liver fibrosis in Japanese patients with MASLD, regardless of diabetes status.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), metabolic dysfunction–associated steatotic liver disease (MONDO:0013209)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, PCDHGA12 (protocadherin gamma subfamily A, 12) [NCBI Gene 26025] {aka CDH21, FIB3, PCDH-GAMMA-A12}, MAF (MAF bZIP transcription factor) [NCBI Gene 4094] {aka AYGRP, CCA4, CTRCT21, c-MAF}
- **Diseases:** Diabetes (MESH:D003920), CAP (MESH:C538265), MASLD (MESH:D008107), VCTE (MESH:D053421), cardiovascular disease (MESH:D002318), allergy (MESH:D004342), Hepatic Steatosis (MESH:D005234), Metabolic Dysfunction-Associated (MESH:D008659), obesity (MESH:D009765), LSM (MESH:D017093), type 2 diabetes (MESH:D003924), NITs (MESH:C537770), HCC (MESH:D006528), cancer (MESH:D009369), -4 fibrosis (MESH:D005355), Liver fibrosis (MESH:D008103)
- **Chemicals:** starch (MESH:D013213), TG (MESH:D013866), triglyceride (MESH:D014280), alcohol (MESH:D000438), Glucose (MESH:D005947), Brown Rice (-), uric acid (MESH:D014527)
- **Species:** Homo sapiens (human, species) [taxon 9606], Oryza sativa (Asian cultivated rice, species) [taxon 4530]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12824083/full.md

---
Source: https://tomesphere.com/paper/PMC12824083