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Published on: June 18, 2020
Mean platelet volume as a fibrosis marker in patients with chronic hepatitis B
Fuat Ekiz1, Osman Yüksel, Erdem Koçak
1Dışkapı Yıldırım Beyazıt Educational and Research Hospital, Department of Gastroenterology, Ankara, Turkey. dr_ekiz@yahoo.com
Insights
Mean platelet volume (MPV) is elevated in patients with chronic hepatitis B (CHB) and correlates with advanced liver fibrosis. While MPV may aid fibrosis assessment in CHB, it is not a standalone diagnostic tool.
Area of Science:
- Hepatology
- Hematology
- Diagnostic Markers
Background:
- Noninvasive tests are crucial for diagnosing liver fibrosis.
- Assessing liver fibrosis score (LFS) in chronic hepatitis B (CHB) is essential for patient management.
- The correlation between mean platelet volume (MPV) and liver fibrosis stage in CHB requires further investigation.
Purpose of the Study:
- To investigate the relationship between MPV and the stage of liver fibrosis in patients with CHB.
- To determine if MPV can serve as a noninvasive marker for advanced fibrosis in CHB patients.
Main Methods:
- Retrospective study of 59 CHB patients and 25 healthy controls.
- Data collected included HBV-DNA, liver function tests, and MPV.
- Patients were categorized into groups with and without advanced fibrosis (F3-F4).
Main Results:
- MPV levels were significantly higher in CHB patients compared to controls (P<0.001).
- MPV was significantly elevated in patients with advanced fibrosis (Group 2) versus those without (Group 1) (P=0.009).
- MPV was independently associated with advanced fibrosis in multivariable analysis (P=0.031).
Conclusions:
- MPV may be a useful indicator for assessing liver fibrosis in CHB patients.
- MPV's nonspecificity necessitates its use in conjunction with other diagnostic tools.
- Further research is needed to validate MPV's role in fibrosis staging.
Introduction:
Many noninvasive tests have been studied for the diagnosis and determining the liver fibrosis score (LFS). In this study, we aimed to research the correlation of mean platelet volume (MPV) and stage of liver fibrosis in patients with chronic hepatitis B (CHB).
Patients And Methods:
Fifty-nine patients with CHB were enrolled retrospectively into the study. Age-sex matched 25 healthy subjects were used as control group. The following data were obtained from computerized patient registry database: HBV-DNA level, hepatitis B e-antigen seropositivity, liver enzymes and function tests, white blood cell count, platelet count, hemoglobin, histological activity index, LFS, and MPV. Patients were divided into two groups: patients without significant fibrosis (F0, F1, or F2) (Group 1) and patients with advanced fibrosis (F3, F4) (Group 2).
Results:
A statistically significant increase in MPV was seen in patients with CHB compared with healthy controls (8.49±0.84 fl vs.7.65±0.42 fl, P<0.001). Receiver operating characteristic curve analysis suggested that the optimum MPV level cut-off points for CHB was 8.0 fl, with sensitivity, specificity, PPV, and NPV of 68, 76, 86, and 50%, respectively. MPV levels were significantly higher in Group 2 (8.91±0.94 fl, P: 0.009) compared with Group 1 (8.32±0.74 fl). ROC curve analysis suggested that the optimum MPV level cut-off points for Group 2 was 8.45 fl, with sensitivity, specificity, positive and negative predictive value of 77, 59, 45, and 85%, respectively. Multivariable logistic regression model, which consisted of HAI, ALT, HBV-DNA, platelet count, and MPV, was performed. We showed that MPV was independently associated with advanced fibrosis (P: 0.031).
Conclusion:
We suggest that MPV might help in the assessment of fibrosis in CHB. It should not be considered a stand-alone test for this use owing to nonspecificity with other diseases.
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