# Analysis of Visfatin Concentration and Other Potential Biomarkers Associated with MASLD Development in Saliva and Serum of Patients with Obesity—A Pilot Study

**Authors:** Beata Zyśk, Joanna Smarkusz-Zarzecka, Urszula Cwalina, Agnieszka Gornowicz, Karolina Orywal, Anna Bielawska, Barbara Mroczko, Lucyna Ostrowska

PMC · DOI: 10.3390/nu18040652 · 2026-02-16

## TL;DR

This pilot study explores salivary visfatin as a potential biomarker for liver disease in obese individuals.

## Contribution

The study identifies salivary visfatin as a possible indicator of MASLD in obesity and explores its correlations with inflammatory markers.

## Key findings

- Salivary visfatin levels were associated with the presence of MASLD in obese individuals.
- Higher salivary interleukin-1β and serum interleukin-6 were linked to elevated visfatin levels.
- Correlations were found between salivary and serum inflammatory markers like IL-6 and MMP-2.

## Abstract

Background/Objectives: Adipokines and cytokines, secreted by adipocytes and immune cells, play key roles in metabolic and inflammatory processes. This study aimed to assess the association between salivary visfatin levels and metabolic dysfunction-associated steatotic liver disease (MASLD), determine a salivary visfatin cutoff associated with increased risk of this disease, and examine correlations among selected adipokines, cytokines, and gelatinases in serum and saliva of obese patients. Methods: The study included 65 participants (40 women and 25 men) with a body mass index (BMI) ranging from 30.0 to 39.9 kg/m2, who were divided into groups based on whether the salivary visfatin concentration exceeded the quantification limit (1.229 ng/mL). Body composition analysis was performed using the bioelectrical impedance method, quantitative assessment of hepatic steatosis was carried out using transient elastography, and the concentrations of selected adipokines, cytokines, and gelatinases were determined in serum and saliva. Results: A relationship was observed between lower BMI and salivary visfatin concentrations below the quantification limit (p = 0.017), and between the absence of MASLD and visfatin levels below the quantification threshold in saliva (p = 0.05). Higher concentrations of interleukin-1β (p = 0.003) and matrix metalloproteinase-2 (p = 0.019) in saliva, as well as interleukin-6 (p = 0.002) in serum, were observed in the group with salivary visfatin levels above the quantification limit. Correlations were found between salivary and serum IL-6 concentrations (r = 0.30; p = 0.016) and between serum resistin and salivary IL-6 levels (r = 0.24; p = 0.056), as well as between serum IL-6 and salivary MMP-2 concentrations (r = 0.24; p = 0.059). Conclusions: In this pilot study, salivary visfatin levels were found to differ between obese individuals with and without MASLD and to be associated with selected anthropometric parameters and inflammatory markers, but the observed associations are exploratory and require confirmation.

## Linked entities

- **Proteins:** NAMPT (nicotinamide phosphoribosyltransferase), IL6 (interleukin 6), LOC114022543 (uncharacterized LOC114022543)
- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, NAMPT (nicotinamide phosphoribosyltransferase) [NCBI Gene 10135] {aka 1110035O14Rik, PBEF, PBEF1, VF, VISFATIN}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** abdominal adiposity (MESH:D000007), Obesity (MESH:D009765), type 1 and type 2 diabetes mellitus (MESH:D003924), Liver Steatosis (MESH:D005234), cholestatic or alcoholic liver disease (MESH:D008108), overweight (MESH:D050177), dementia (MESH:D003704), Associated (MESH:D018886), eating disorders (MESH:D001068), liver conditions (MESH:D017093), periodontal disease (MESH:D010510), multiple sclerosis (MESH:D009103), metabolic disorders (MESH:D008659), hypertriglyceridemia (MESH:D015228), systemic diseases (MESH:D034721), fibrosis (MESH:D005355), injury to (MESH:D014947), Inflammatory (MESH:D007249), MASLD (MESH:D008107), viral hepatitis (MESH:D014777), II (MESH:C537730), blood pressure (MESH:D006973), diabetes (MESH:D003920), endocrine or hormonal disorders (MESH:D004700), NAFLD (MESH:D065626), insulin resistance (MESH:D007333), impaired glucose metabolism (MESH:D044882), hepatic fibrosis (MESH:D008103)
- **Chemicals:** water (MESH:D014867), lipid (MESH:D008055), glucose (MESH:D005947), CAP (-), carbohydrates (MESH:D002241), triglyceride (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943479/full.md

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Source: https://tomesphere.com/paper/PMC12943479