# Eating behaviors and liver health in metabolic dysfunction-associated fatty liver disease: the serial mediating roles of Mediterranean diet adherence and adiposity

**Authors:** Büşra Başar Gökcen, İrem Kurtuluş, Nermin Kabak, Ferenc Budan, Duygu Ağagündüz, Dávid Szép

PMC · DOI: 10.3389/fnut.2026.1740363 · Frontiers in Nutrition · 2026-02-10

## TL;DR

This study shows how eating behaviors affect liver health through diet adherence and body fat, especially in people with a liver condition called MAFLD.

## Contribution

The study identifies serial mediation pathways involving Mediterranean diet adherence and adiposity in the link between eating behaviors and liver health in MAFLD.

## Key findings

- MAFLD individuals had higher BMI, VAI, and ALT levels compared to non-MAFLD individuals.
- Uncontrolled eating scores were linked to higher ALT levels via BMI and Mediterranean diet adherence in MAFLD individuals.
- Mindful eating scores did not show significant moderated mediation effects on liver health.

## Abstract

This study aimed to investigate the mediating roles of healthy diet adherence and adiposity in the relationship between eating behaviors (uncontrolled or mindful eating) and liver health according to metabolic dysfunction-associated fatty liver disease (MALFD) status.

Adults with and without MAFLD (150 and 90, respectively) were included. Eating behaviors were assessed using the Mindful Eating Questionnaire (MEQ) and Three-Factor Eating Questionnaire (TFEQ), and Mediterranean diet adherence was measured with the Mediterranean Diet Adherence Screener (MEDAS). Adiposity indices included Body Mass Index (BMI) and Visceral Adiposity Index (VAI). Liver health markers were alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Statistical analyses comprised group comparisons, Spearman correlations, and serial mediation models tested using Hayes’ PROCESS macro.

Individuals with MAFLD had higher BMI (median 32 vs. 25 kg/m2), VAI (4.1 vs. 1.1), and ALT levels (83 vs. 20 U/L, all p < 0.001). In unadjusted comparisons, the MAFLD group showed lower MEQ and MEDAS scores, together with higher emotional eating and uncontrolled eating scores on the TFEQ. In multivariable logistic regression analyses, BMI was independently associated with MAFLD status (OR = 1.43, 95% CI: 1.30–1.57), while eating behavior scores were not significant after BMI adjustment. Serial mediation analyses using PROCESS Model 6 showed that the association between uncontrolled eating scores and ALT levels was indirectly transmitted through BMI, with the serial indirect pathway involving MEDAS and BMI reaching statistical significance in the MAFLD group (indirect effect = 0.106; 95% bootstrap CI: 0.019–0.251). Moderated mediation analyses using PROCESS Model 92 further indicated a significant index of moderated mediation for this pathway (IMM = 0.090; 95% bootstrap CI: 0.003–0.233), whereas mediation models based on mindful eating scores did not yield significant moderated mediation effects.

The results support the presence of indirect associations linking eating behavior scores to liver enzyme levels via Mediterranean diet adherence and adiposity, particularly in the context of MAFLD. These pathways point to potentially modifiable behavioral and dietary targets, while underscoring the need for confirmation through prospective and interventional studies.

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** ALT (MESH:C536414), metabolic (MESH:D008659), abdominal obesity (MESH:D056128), VAI (MESH:D007418), obese (MESH:D009765), NASH (MESH:D005235), Adiposity (MESH:D018205), type 2 diabetes (MESH:D003924), Fatty Liver (MESH:D005234), Liver health (MESH:D017093), Uncontrolled eating (MESH:D001068), hepatocellular injury (MESH:D056486), cardiovascular disease (MESH:D002318), NAFLD (MESH:D065626), insulin resistance (MESH:D007333), weight loss (MESH:D015431), hepatic fibrosis (MESH:D008103), binge eating (MESH:D002032), metabolic syndrome (MESH:D024821), fibrosis (MESH:D005355), inflammatory (MESH:D007249), Liver Diseases (MESH:D008107), Disease (MESH:D004194), dyslipidemia (MESH:D050171), metabolically unhealthy obesity (MESH:D000067329), hypertension (MESH:D006973)
- **Chemicals:** alcohol (MESH:D000438), cholesterol (MESH:D002784), omega 6 fatty acids (MESH:D043371), lipid (MESH:D008055), MUFA (MESH:D005229), TG (MESH:D014280), Ind1 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929163/full.md

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Source: https://tomesphere.com/paper/PMC12929163