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Published on: September 30, 2021
Comprehensive clinical assessment improves the accuracy of predicting cirrhosis in chronic hepatitis C
Adam Gordon1, Michael J Bailey, Peter R Gibson
1Department of Gastroenterology, Alfred Hospital, Commercial Road, Prahran, Victoria 3181, Australia.
Insights
A comprehensive clinical assessment combining clinical markers, the discriminant score, and serum hyaluronic acid accurately predicts cirrhosis in chronic hepatitis C patients, offering a non-invasive diagnostic alternative.
Area of Science:
- Hepatology
- Clinical Diagnostics
- Biomarker Research
Background:
- Diagnosing cirrhosis in chronic hepatitis C (CHC) is crucial but challenging without liver biopsy.
- Non-invasive methods are needed to assess liver fibrosis in CHC patients.
Purpose of the Study:
- To compare the predictive accuracy of individual clinical markers, the discriminant score (DS), and serum hyaluronic acid (HA) for cirrhosis in CHC.
- To evaluate the combined performance of these markers in predicting cirrhosis.
Main Methods:
- Retrospective analysis of 151 CHC patients undergoing liver biopsy.
- Development and validation of a clinical examination score (CES), calculation of DS, and assay of serum HA.
- Construction of combination scores integrating CES, DS, and serum HA score (HAS).
Main Results:
- Serum HA demonstrated higher accuracy than CES or DS alone in predicting cirrhosis.
- The combination of CES, DS, and HAS achieved the highest accuracy, with 78% sensitivity and 93% specificity.
- Positive and negative predictive values for the combined score were 75% and 94%, respectively.
Conclusions:
- A comprehensive clinical assessment using combined clinical and laboratory data offers superior prediction of cirrhosis in CHC compared to individual markers.
- This integrated approach provides a more accurate, non-invasive method for diagnosing cirrhosis in CHC patients.
Background:
The diagnosis of cirrhosis in chronic hepatitis C (CHC) is important but difficult in those who are unable to undergo liver biopsy. Thus, the aims of the present study were to compare separately and in combination, clinical markers of liver disease, the discriminant score (DS) and serum hyaluronic acid (HA) for their ability to predict cirrhosis in CHC.
Methods:
Two groups of consecutive patients (groups 1 and 2) with CHC were analyzed. Clinical data and routine laboratory results at the time of liver biopsy were collected, and serum HA levels were assayed. A clinical examination score (CES) was constructed using the sum of clinical markers of liver disease in group 1 and was validated in group 2, the DS was calculated, and a serum HA score (HAS) was produced. Combination scores were constructed using the sum of the CES, DS and HAS. Histological analysis of liver biopsies was performed by hepatopathologists blinded to clinical results.
Results:
One hundred and fifty-one patients with CHC (group 1, n = 47; group 2, n = 104) including 27 with cirrhosis were assessed. Serum HA was more accurate than either CES or DS in the prediction of cirrhosis. The combination of CES, DS and HAS enabled the most accurate prediction of cirrhosis with a sensitivity and specificity of 78% and 93%, and a positive predictive value and negative predictive value of 75% and 94%, respectively.
Conclusions:
A comprehensive clinical assessment utilizing clinical and laboratory data more accurately predicts the presence and absence of cirrhosis in CHC than individual markers.
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