Circulating vascular adhesion protein-1(VAP-1): a possible biomarker for liver fibrosis associated with chronic

Zehra Öksüz1, Enver Üçbilek2, Mehmet Sami Serin3

  • 1Department of Pharmaceutical Microbiology, Mersin University Faculty of Pharmacy, Mersin, Turkey. zehraoksz@gmail.com.

Insights

Vascular adhesion protein-1 (VAP-1) levels increase with fibrosis severity in chronic hepatitis B patients, suggesting VAP-1 as a biomarker for fibrogenesis. Levels were higher in CHB than CHC patients.

Area of Science:

  • Hepatology
  • Biomarker Discovery
  • Immunology

Background:

  • Vascular adhesion protein-1 (VAP-1) is implicated in chronic liver diseases and fibrogenesis.
  • Understanding VAP-1's role in disease progression is crucial for developing noninvasive diagnostic tools.

Purpose of the Study:

  • To investigate the association between VAP-1 levels and the severity of fibrosis, cirrhosis, and hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) and C (CHC) patients.
  • To evaluate VAP-1 as a potential noninvasive biomarker for monitoring liver disease progression.

Main Methods:

  • Serum VAP-1 concentrations were measured using ELISA in CHB and CHC patients across different fibrosis stages (F0-F4), cirrhosis, and HCC.
  • VAP-1 levels were compared between fibrosis stages and disease types.

Main Results:

  • VAP-1 levels significantly increased with fibrosis progression in CHB patients, peaking at stage F4 (severe fibrosis).
  • A significant difference in VAP-1 was observed between F0 and F4 in CHB, but not between F1 and F4 in CHC.
  • No significant difference in VAP-1 levels was found between cirrhosis and HCC patients for either CHB or CHC.
  • VAP-1 levels were generally higher in CHB than in CHC patients.

Conclusions:

  • VAP-1 levels may serve as a noninvasive biomarker for assessing fibrogenesis severity in chronic hepatitis B infection.
  • Further research is warranted to explore VAP-1's utility in CHC and its correlation with other liver disease markers.

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