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The relationship between HBV-DNA level and histology in patients with naive chronic HBV infection
Rukiye Vardar1, Fulya Gunsar, Ruchan Sertoz
1Ege University School of Medicine, Department of Gastroenterology, Izmir, Turkey. rukiye.vardar@ege.edu.tr
Insights
A serum hepatitis B virus DNA (HBV-DNA) level of 15,000 copies/mL can help identify patients with chronic hepatitis B (CHB) who have low disease activity. These patients may not require liver biopsy, simplifying their management.
Area of Science:
- Hepatology
- Virology
- Gastroenterology
Background:
- Accurate staging of hepatic fibrosis is crucial for managing chronic hepatitis B (CHB).
- Hepatitis B virus DNA (HBV-DNA) levels are increasingly recognized as important prognostic markers in CHB.
- Understanding the correlation between HBV-DNA and liver histology aids in risk stratification.
Purpose of the Study:
- To investigate the relationship between serum HBV-DNA levels and liver histology in CHB patients.
- To determine a threshold HBV-DNA level for differentiating low-risk from high-risk patients for disease progression.
Main Methods:
- Evaluation of 259 treatment-naïve CHB patients with HBV-DNA > 2000 copies/mL.
- Liver biopsies assessed histopathologically using the Ishak scoring system.
- Regular monitoring of liver enzymes (AST, ALT) and highest values recorded.
Main Results:
- The study included 259 patients (60% male, mean age 40).
- Mean HBV-DNA level was 5.9 log copies/mL; mean fibrosis score was 1.38.
- An HBV-DNA threshold of 15,000 copies/mL was identified, below which patients typically showed low fibrosis and inflammation (fibrosis score < 2, grade ≤ 5).
Conclusions:
- Serum HBV-DNA levels ≤ 15,000 copies/mL are associated with low histological activity in CHB patients.
- These patients may not require liver biopsy, irrespective of their hepatitis B e-antigen (HBeAg) status.
- This finding can help streamline CHB patient management and reduce the need for invasive procedures.
Background:
In patients with chronic hepatitis B (CHB) infection, precise definition of the hepatic fibrosis stage is the most important parameter to assess the risk of disease progression. Correlation between the prognosis of the CHB and the level of hepatitis-B virus DNA (HBV-DNA) is well considered in recent years.
Aims:
The aim of this study is to investigate the relationship between serum HBV-DNA level and histology of the liver. We also wanted to determine a threshold level of HBV-DNA for differentiation of low and high risk patients for progression.
Methods:
Two-hundred-fifty-nine patients with serum HBV-DNA level > 2000 copies/mL, determined by polymerase chain reaction (PCR), and biopsy proven naïve CHB infection were evaluated. Liver biopsies were evaluated histopathologically according to the Ishak scoring system. Laboratory values such as aspartate aminotransferase (AST), alanine aminotransferase ratio (ALT) were tested every 3 months and the highest value of each patient was evaluated.
Results:
Mean age was 40 +/- 11 and 60% (155/259) of the patients were male. Mean laboratory values were as follows: AST: 52 +/- 46 U/L, ALT: 93 +/- 133 U/L, PLT: 224 +/- 60 1093)/l HBV DNA: 5.9 +/- 1.5 log copies/mL. In histological evaluation, mean inflammatory score was 4.34 +/- 2.72 and fibrosis score was 1.38 +/- 1.46. The fibrosis score was 0 or 1 in 63.3% (164/259) of the patients. The relationship between HBV-DNA level and histologic grade/stage was investigated and 15.000 copies/mL HBV DNA level was found as the threshold level to describe the activity of the disease. Fibrosis score was < 2 and/or grade < or = 5 in the patients who have HBV-DNA value below that level.
Conclusion:
In patients who have serum HBV-DNA level < or = 15000/copies/mL, histological activity was almost always low, and it seems that these patients do not need a liver biopsy regardless of hepatitis-B-e antigen (HBeAg) status.
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