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The validity of serum markers for fibrosis staging in chronic hepatitis B and C
1Henry Ford Health System, Detroit, MI, USA.
Insights
The FIB-4 score accurately assesses liver fibrosis in chronic hepatitis B (CHB) and chronic hepatitis C (CHC) patients. This non-invasive method aids in managing liver disease by predicting advanced fibrosis and cirrhosis.
Area of Science:
- Hepatology
- Biomarker Development
- Diagnostic Accuracy
Background:
- Accurate assessment of liver fibrosis is crucial for managing chronic hepatitis B (CHB) and chronic hepatitis C (CHC).
- Non-invasive serum markers offer a reproducible and accessible alternative to liver biopsy for fibrosis staging.
- Existing serum marker indices require validation and optimization for clinical application.
Purpose of the Study:
- To expand and validate serum marker indices for accurate, reproducible, and easily applied liver fibrosis assessment.
- To derive and validate optimal cut-offs for differentiating fibrosis levels using a novel algorithm.
- To compare the predictive performance of FIB-4 and APRI scores in CHB and CHC patients.
Main Methods:
- Liver biopsy results from 284 CHB and 2304 CHC patients were mapped to an F0-F4 fibrosis scale.
- APRI and FIB-4 scores were calculated within a 6-month window of biopsy and mapped to the same scale.
- A novel algorithm was used to derive and validate optimal cut-offs for fibrosis level differentiation.
Main Results:
- The FIB-4 score demonstrated superior prediction of advanced fibrosis and cirrhosis in CHC patients compared to other serum markers.
- FIB-4 showed similar performance to APRI in CHB patients for predicting advanced fibrosis and cirrhosis.
- The area under the receiver operating characteristic curves (AUROC) for FIB-4 was 0.86 for CHB and 0.83 for CHC in differentiating F3-F4 from F0-F2.
- Validated FIB-4 cut-offs yielded high positive predictive values for identifying non-fibrotic (F0-F2) and cirrhotic (F4) stages.
Conclusions:
- The FIB-4 score accurately predicts the upper and lower ends of liver fibrosis stages (cirrhosis and F0-F2) in both CHB and CHC patients.
- FIB-4 serves as a reliable non-invasive tool for assessing liver fibrosis, supporting individualized disease management.
- Optimized FIB-4 cut-offs enhance its utility in clinical practice for diagnosing liver fibrosis stages.
Abstract:
Assessment of liver fibrosis is critical for successful individualized disease management in persons with chronic hepatitis B (CHB) or chronic hepatitis C (CHC). We expanded and validated serum marker indices to provide accurate, reproducible and easily applied methods of fibrosis assessment. Liver biopsy results from over 284 CHB and 2304 CHC patients in the Chronic Hepatitis Cohort Study ('CHeCS') were mapped to a F0-F4 equivalent scale. APRI and FIB-4 scores within a 6-month window of biopsy were mapped to the same scale. A novel algorithm was applied to derive and validate optimal cut-offs for differentiating fibrosis levels. For the prediction of advanced fibrosis and cirrhosis, the FIB-4 score outperformed the other serum marker indices in the CHC cohort and was similar to APRI in the CHB cohort. The area under the receiver operating characteristic curves (AUROC) for FIB-4 in differentiating F3-F4 from F0-F2 was 0.86 (95% CI: 0.80-0.92) for CHB and 0.83 (95% CI: 0.81-0.85) for CHC. The suggested cut-offs based on FIB-4 model produced high positive predictive values [CHB: 90.0% for F0-F2, 100.0% for cirrhosis (F4); CHC: 89.7% for F0-F2; 82.9% for cirrhosis (F4)]. In this large observational cohort, FIB-4 predicted the upper and lower end of liver fibrosis stage (cirrhosis and F0-F2, respectively) with a high degree of accuracy in both CHB and CHC patients.
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