# Association of Serum Selenium with Clinical Features and Inflammatory and Oxidative Stress Markers in Iranian Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease—A Cross-Sectional Study

**Authors:** Abbas Pishdadian, Reza Sharifi, Adele Shafaghi, Soudabeh Hamedi-Shahraki, Farshad Amirkhizi, Aleksandra Klisic

PMC · DOI: 10.3390/diagnostics15121559 · Diagnostics · 2025-06-18

## TL;DR

This study found that lower selenium levels in Iranian patients with liver disease are linked to higher inflammation, more oxidative stress, and worse liver fat buildup.

## Contribution

The study provides new evidence linking serum selenium levels to liver disease severity and inflammatory/oxidative stress markers in Iranian MASLD patients.

## Key findings

- Lower selenium levels correlated with more severe liver steatosis and higher oxidative stress markers.
- Higher selenium levels were associated with better antioxidant capacity and lower insulin resistance.
- No significant trends were found for some inflammatory markers like IL-6 and TGF-β.

## Abstract

Background: There are conflicting epidemiological studies regarding the association between selenium (Se) and metabolic disorders. Furthermore, the pathophysiological links between Se and metabolic dysfunction-associated steatotic liver disease (MASLD) have not yet been fully elucidated. Therefore, we evaluated the association between serum Se levels and the clinical features of MASLD and the inflammatory and oxidative stress markers in these patients as potential risk factors for the progression of this disease. Methods: This cross-sectional study involved 150 patients aged 20 to 50 years who were newly diagnosed with MASLD. Oxidative stress was evaluated by measuring serum thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), and the activities of erythrocyte superoxide dismutase (SOD) and glutathione peroxidase (GPx). Tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and transforming growth factor beta (TGF-β) were measured as inflammatory markers. A one-way analysis of variance (ANOVA), Pearson chi-square test, Kruskal–Wallis test, and multiple linear regression were employed for data analysis. Results: We observed a significant inverse association between serum Se concentrations and liver steatosis severity in the participants. There was a significant decrease in serum concentrations of insulin and the homeostasis model assessment of insulin resistance (HOMA-IR), triglycerides, TNF-α, and TBARS with ascending quartiles of serum Se. Conversely, the mean serum levels of TAC and erythrocyte GPx activities exhibited a consistent increasing trend in relation to rising serum Se concentrations. However, no significant trends were identified for serum FSG, IL-6, TGF-β, or erythrocyte SOD activities across the varying levels of serum Se. Conclusions: Our results demonstrate that decreased serum selenium levels in Iranian patients with MASLD correlate with elevated inflammatory markers, increased oxidative stress, and more severe liver steatosis.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL6 (interleukin 6), TGFB1 (transforming growth factor beta 1), SOD1 (superoxide dismutase 1), GPX (probable phospholipid hydroperoxide glutathione peroxidase)
- **Chemicals:** selenium (PubChem CID 6326970), insulin (PubChem CID 70678557)
- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), MASLD (MONDO:0013209)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}
- **Diseases:** Metabolic Dysfunction (MESH:D008659), Inflammatory (MESH:D007249), insulin resistance (MESH:D007333), MASLD (MESH:D008107), liver steatosis (MESH:D005234)
- **Chemicals:** triglycerides (MESH:D014280), TBARS (MESH:D017392), Se (MESH:D012643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12191626/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12191626/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12191626/full.md

---
Source: https://tomesphere.com/paper/PMC12191626