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Updated: Jun 3, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
Association between Hepatitis B Virus X Gene Mutations and Clinical Status in Patients with Chronic Hepatitis B
Eun Young Cho1, Chang Soo Choi, Ji-Hyun Cho
1Department of Internal Medicine, Wonkwang University Hospital, Wonkwang University College of Medicine, Iksan, Korea.
Insights
Specific mutations in the hepatitis B virus (HBV) X gene are linked to disease progression in patients with chronic HBV infection. These HBV X gene mutations correlate with clinical status, including cirrhosis and hepatocellular carcinoma (HCC).
Area of Science:
- Hepatology
- Virology
- Molecular Biology
Background:
- Hepatitis B virus (HBV) infection is a global health concern.
- The HBV X gene plays a crucial role in viral replication and pathogenesis.
- Limited data exists on the association between entire HBV X gene mutations and clinical outcomes.
Purpose of the Study:
- To investigate the association between mutations in the complete HBV X gene and the clinical status of HBV genotype C infected patients.
- To compare the prevalence of X gene mutations across different stages of chronic HBV infection: chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma (HCC).
Main Methods:
- Direct sequencing was used to analyze HBV X genes from 194 patients.
- The study population included patients with chronic hepatitis (n=60), liver cirrhosis (n=65), and HCC (n=69).
- Sequencing results were compared among the three clinical groups.
Main Results:
- Several HBV X gene mutations (G1386M, C1485T, C1653T, T1753V, A1762T, G1764A) showed significant associations with clinical status.
- Mutations T1753V and A1762T/G1764A were more frequent in Hepatitis B e antigen (HBeAg)-negative patients.
- Specific mutations (G1386M, C1653T, A1762T/G1764A) were more prevalent in cirrhosis and HCC patients compared to chronic hepatitis patients.
- The T1753V mutation showed a significant increase in prevalence with disease progression from cirrhosis to HCC.
Conclusions:
- Distinct patterns of HBV X gene mutations are associated with varying clinical statuses in chronic HBV infection.
- These findings highlight the potential role of specific X gene mutations as biomarkers for HBV disease progression.
Background/Aims:
Few reports have described the association between mutations in the entire X gene of the hepatitis B virus (HBV) and the clinical status of HBV-infected patients. We studied the association between HBV X gene mutations and the disease status of patients infected with HBV genotype C.
Methods:
Mutations in the HBV X genes of 194 patients were determined by direct sequencing. The subject population consisted of patients with chronic hepatitis (n=60), liver cirrhosis (n=65), and hepatocellular carcinoma (HCC) (n=69). The sequencing results of these 3 groups were compared.
Results:
Each of the mutations G1386M, C1485T, C1653T, T1753V, A1762T, and G1764A was significantly associated with the patient's clinical status. The T1753V (p<0.001) and A1762T/G1764A (p<0.001) mutations were found more frequently in Hepatitis B e antigen (HBeAg)-negative than in HBeAg-positive patients. Specific X gene mutations (G1386M, C1653T, and A1762T/G1764A) were more prevalent in patients with liver cirrhosis and HCC than in chronic hepatitis patients (p<0.005 for all). In addition, the T1753V (p<0.001) and C1485T (p<0.001) mutations were significantly more prevalent in HCC patients than in chronic hepatitis patients. Only the prevalence of the T1753V mutation increased as the HBV infection progressed from liver cirrhosis to HCC (p=0.023).
Conclusions:
Our findings show a difference in the pattern of X gene mutations that were associated with the clinical status of patients with chronic HBV infection.
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