Correlation of Serum M-CSF, CER, and TIMP-1 Levels with Liver Fibrosis in Viral Hepatitis

Hairong Yao1, Xuan Yang2, Man Yan3

  • 1Department of Cardiology, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, Shaanxi 710018, China.

Abstract

Insights

This study shows that serum levels of macrophage colony-stimulating factor (M-CSF), tissue inhibitor of matrix metalloproteinase (TIMP-1), and ceruloplasmin (CER) correlate with liver fibrosis in chronic hepatitis B (CHB) patients. Combined detection of these markers improves diagnostic accuracy for liver fibrosis.

Area of Science:

  • Hepatology
  • Biochemistry
  • Immunology

Background:

  • Chronic hepatitis B (CHB) is a significant cause of liver fibrosis.
  • Accurate assessment of liver fibrosis is crucial for patient management.
  • Biomarkers for non-invasively staging liver fibrosis are needed.

Purpose of the Study:

  • To investigate the relationship between liver fibrosis in CHB and serum levels of macrophage colony-stimulating factor (M-CSF), tissue inhibitor of matrix metalloproteinase (TIMP-1), and ceruloplasmin (CER).
  • To evaluate the diagnostic utility of these markers, individually and in combination, for assessing liver fibrosis severity.

Main Methods:

  • Serum levels of M-CSF, CER, and TIMP-1 were measured in CHB patients and healthy controls.
  • CHB patients were stratified into four fibrosis groups (S1-S4).
  • Statistical analyses correlated marker levels with fibrosis stage and assessed diagnostic performance using Area Under the Curve (AUC).

Main Results:

  • Serum M-CSF and TIMP-1 levels were elevated, while CER levels were decreased in CHB patients compared to controls.
  • Significant differences in M-CSF, CER, TIMP-1, and other fibrosis markers (HA, PC-III, C-IV, LN) were observed across fibrosis stages.
  • Progressive liver fibrosis was associated with increasing M-CSF, TIMP-1, and decreasing CER levels, with significant correlations.

Conclusions:

  • Serum M-CSF, CER, and TIMP-1 levels are significantly associated with the degree of liver fibrosis in CHB patients.
  • The combined assessment of M-CSF, CER, and TIMP-1 demonstrates superior diagnostic significance for staging liver fibrosis compared to individual markers.
  • These markers offer potential as non-invasive tools for monitoring liver fibrosis progression in CHB.

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