# Cystatin C Mirrors Fibrosis Burden in Metabolic Syndrome: Insights from the Metabolic Dysfunction-Associated Fibrosis-5 Score

**Authors:** Musa Salmanoğlu, Sinan Kazan, Elif Yıldırım Ayaz, Süleyman Kılıç, Elif Kazan, Sena Ulu

PMC · DOI: 10.3390/metabo16010071 · 2026-01-13

## TL;DR

This study finds that Cystatin C levels increase with higher MAF-5 scores in metabolic syndrome patients, suggesting a link between liver fibrosis and systemic inflammation.

## Contribution

First investigation of the relationship between MAF-5 scores and Cystatin C levels in metabolic syndrome patients.

## Key findings

- Cystatin C levels correlated positively with MAF-5 scores (r = 0.357, p < 0.001).
- Cystatin C levels increased significantly across higher MAF-5 quartiles (p < 0.001).
- Combined MAF-5 and Cystatin C assessment may improve risk stratification for hepatic fibrosis.

## Abstract

Background: Metabolic syndrome (MetS) comprises interrelated metabolic abnormalities that collectively confer increased risk of cardiovascular disease and hepatic morbidity. The MAF-5 score is a non-invasive prognostic marker of liver fibrosis and mortality, while Cystatin C (CysC) is a sensitive indicator of renal function that also reflects inflammation, atherosclerosis, and metabolic dysfunction. Although both MetS and CysC have been widely studied, their potential interplay via MAF-5 remains unclear. We aimed to investigate the relationship between MAF-5 scores and CysC levels in MetS patients for the first time. Materials and Methods: Adults (≥18 years) with MetS were included in this study. MAF-5 scores (based on waist circumference, BMI, diabetes status, AST, and platelet count) and CysC levels were recorded. The MAF-5–CysC relationship was assessed via Pearson correlation. Participants were grouped into MAF-5 quartiles, and continuous variables were compared using ANOVA with Bonferroni-corrected pairwise tests. Results: We included 347 MetS patients (54.8% female, median age 54 years). The median MAF-5 score was 1.25, and MAF-5 correlated positively with CysC (r = 0.357, p < 0.001). CysC levels differed significantly across MAF-5 quartiles (Q1 = 0.96, Q2 = 0.99, Q3 = 1.06, Q4 = 1.09; p < 0.001), with Q4 showing higher values than Q1 and Q2. Conclusions: A significant correlation was found between MAF-5 scores and CysC in patients with MetS. CysC levels differed significantly across MAF-5 quartiles, suggesting a potential link between systemic inflammation, liver fibrosis, and CysC. These results highlight shared inflammatory and fibrotic pathways, underlying metabolic dysfunction. Clinically, combined assessment of MAF-5 and CysC may improve risk stratification, identifying patients at higher risk for hepatic fibrosis and adverse outcomes.

## Linked entities

- **Proteins:** CYSTATIN-C (cystatin-C)
- **Diseases:** metabolic syndrome (MONDO:0000816), cardiovascular disease (MONDO:0004995), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, CST3 (cystatin C) [NCBI Gene 1471] {aka ADLDWA, ARMD11, HEL-S-2}
- **Diseases:** cardiovascular disease (MESH:D002318), atherosclerosis (MESH:D050197), MetS (MESH:D024821), diabetes (MESH:D003920), Metabolic Dysfunction (MESH:D008659), inflammation (MESH:D007249), hepatic fibrosis (MESH:D008103), Fibrosis (MESH:D005355), CysC. (OMIM:211750)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12843606/full.md

---
Source: https://tomesphere.com/paper/PMC12843606