# The development and evaluation of nine non-conventional lipid parameters for metabolic dysfunction-associated fatty liver disease in Chinese medical health examination adults: a single-center retrospective study

**Authors:** Lian Song, Lirong Zhang, Yinhui Hang, Zijie Yang, Jing Yang, Dongqing Wang

PMC · DOI: 10.3389/fnut.2026.1788704 · 2026-02-25

## TL;DR

This study identifies TyG-BMI as a strong predictor of MAFLD and cardiovascular risk in adults, using electronic health records from a Chinese population.

## Contribution

The study introduces TyG-BMI as a novel and effective non-conventional lipid parameter for predicting MAFLD and associated cardiovascular risk.

## Key findings

- TyG-BMI showed the strongest association with MAFLD (OR = 3.7) and highest predictive performance (AUC = 0.81).
- A nonlinear relationship between TyG-BMI and MAFLD was identified with an inflection point at 222.426.
- Higher TyG-BMI tertiles were linked to increased atherosclerotic cardiovascular disease risk (OR = 2.55).

## Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) represents a prevalent chronic hepatic condition globally, characterized by hepatic steatosis concurrent with at least one cardiometabolic risk factor, such as overweight/obesity, type 2 diabetes mellitus (T2DM), or metabolic dysregulation. This study aimed to evaluate the associations between nine non-conventional lipid parameters—BMI, NHHR, AIP, RC, GHR, CHG, LCI, TyG, TyG-BMI—and MAFLD, and to compare their predictive performance for MAFLD screening.

This study utilized the electronic medical record at Wuhan Union Hospital between January 2020 and November 2021, and multi-model adjustment weighted logistic regression analysis was applied to investigate the association of the nine parameters with MAFLD. Receiver operating characteristic (ROC) curves were analyzed to assess the screening ability of the nine parameters. Furthermore, the association between the most predictive parameter and MAFLD was investigated with RCS analysis, and differences in risk across populations were explored with subgroup analyses.

A total of 1,592 participants were included in the final analysis, among whom 937 (58.86%) were diagnosed with MAFLD. Multivariable logistic regression identified NHHR, BMI, AIP, RC, GHR, LCI, TyG, and TyG-BMI as independent risk factors for MAFLD, with TyG-BMI demonstrating the strongest association (OR = 3.7, 95% CI: 3.05–4.48). The area under the ROC curve (AUC) for TyG-BMI was 0.81, and its predictive performance was significantly superior to that of the other parameters (all P < 0.001 by DeLong’s test). RCS analysis revealed a nonlinear relationship between TyG-BMI and MAFLD (P for nonlinearity<0.001), with an identified inflection point at a TyG-BMI value of 222.426. Additionally, MAFLD patients in the highest TyG-BMI tertile exhibited a significantly increased risk of atherosclerotic cardiovascular disease (ASCVD) compared to those in the lowest tertile (OR = 2.55, 95% CI: 1.337–4.91) after adjustment for confounders.

The evaluated non-conventional lipid parameters, particularly TyG-BMI, are useful indicators for MAFLD identification. TyG-BMI demonstrated the strongest predictive ability for MAFLD and was independently associated with ASCVD risk in affected individuals. Elevated TyG-BMI may therefore serve as a clinically accessible marker for identifying individuals at high risk of MAFLD and for stratifying cardiovascular risk in patients with established MAFLD.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), atherosclerotic cardiovascular disease (MONDO:1060134)

## Full-text entities

- **Genes:** AIP (AHR interacting HSP90 co-chaperone) [NCBI Gene 9049] {aka ARA9, FKBP16, FKBP37, PITA1, SMTPHN, XAP-2}, GHR (growth hormone receptor) [NCBI Gene 2690] {aka GHBP, GHIP}
- **Diseases:** T2DM (MESH:D003924), hepatic condition (MESH:D056486), ASCVD (MESH:D050197), MAFLD (MESH:D005234), overweight/obesity (MESH:D050177), metabolic dysregulation (MESH:D021081)
- **Chemicals:** lipid (MESH:D008055), TyG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976015/full.md

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Source: https://tomesphere.com/paper/PMC12976015