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Published on: February 10, 2015
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.
Objective:
This research is aimed at investigating the relationship between liver fibrosis in viral hepatitis and macrophage colony-stimulating factor (M-CSF), tissue inhibitor of matrix metalloproteinase (TIMP-1), and ceruloplasmin (CER) in serum level.
Methods:
Patients were randomly selected among those admitted to our hospital, and 60 healthy volunteers were chosen to serve as control participants. The levels of serum M-CSF, CER, and TIMP-1 were compared. According to the severity of their liver fibrosis, patients with CHB were separated into four groups: S1, S2, S3, and S4. Serum levels of M-CSF, CER, and TIMP-1 were correlated with liver fibrosis and hepatitis markers, and the diagnostic usefulness of the three indices was assessed with liver cirrhosis patients.
Results:
Increases in M-CSF and TIMP-1 in the CHB group but decreases in CER were statistically significant (P < 0.05). Serum levels of M-CSF, CER, TIMP-1, HA, PC-III, C-IV, and LN differed significantly across the four study groups (P < 0.05). Over time, as liver fibrosis worsened, we observed a progressive uptick in M-CSF, TIMP-1, LN, HA, C-IV, and PC-III levels and a progressive downtick in CER levels, with significant (P < 0.05) differences between the groups. There was a significant positive correlation between liver fibrosis and serum M-CSF, PC-III, TIMP-1, HA, LN, and C-IV levels in the CHB group (P < 0.05) and a significant negative correlation between serum CER and these same factors (P < 0.05). The AUC of 0.956 for diagnosing the S4 stage was greater than that of 0.857, 0.851, and 0.817 for M-CSF, CER, and TIMP-1, respectively.
Conclusions:
In CHB patients, the liver fibrosis degree is associated with the M-CSF, CER, and TIMP-1 levels, and the combined clinical detection of these three markers has better diagnostic significance.
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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