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Updated: Apr 29, 2026

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Published on: March 24, 2023
[Endothelial dysfunction gene polymorphisms and the rate of liver fibrosis in chronic hepatitis C]
Insights
The TT genotype of the CYBA gene is linked to faster fibrosis progression in chronic hepatitis C (CHC) patients. This finding suggests it may be a marker for a poorer CHC disease course.
Area of Science:
- Genetics
- Hepatology
- Molecular Biology
Background:
- Chronic hepatitis C (CHC) is a significant cause of liver fibrosis and cirrhosis.
- Genetic factors may influence the rate of fibrosis progression in CHC.
- Polymorphisms in genes like CYBA, NOS3, and MTHFR are potential determinants of disease severity.
Purpose of the Study:
- To investigate the association between specific gene polymorphisms (CYBA, NOS3, MTHFR) and the rate of liver fibrosis progression in CHC patients.
- To identify genetic markers that could predict rapid fibrosis advancement in CHC.
- To evaluate the role of CYBA C242T, NOS3, and MTHFR gene variants in CHC pathogenesis.
Main Methods:
- A cohort of 109 CHC patients with documented fibrosis stages were analyzed.
- Patients were categorized into rapid (≥0.130 units/year) and slow (<0.130 units/year) fibrosis progression groups.
- Gene polymorphisms were determined using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis, with 299 healthy donors as a control group.
Main Results:
- The TT genotype of the CYBA gene (C242T locus) was significantly more prevalent in patients with rapidly progressive fibrosis compared to those with slow progression (OR 9.09, p=0.0161).
- No significant differences in the distribution of NOS3 and MTHFR gene alleles or genotypes were observed between the rapid and slow fibrosis progression groups.
- The CYBA TT genotype emerged as a potential indicator of accelerated fibrosis in CHC.
Conclusions:
- The TT genotype of the CYBA gene at the C242T locus is associated with a profibrogenic effect in CHC.
- This specific CYBA genotype may serve as a marker for predicting a more severe or aggressive course of chronic hepatitis C.
- Further research into CYBA's role could inform personalized treatment strategies for CHC patients.
Aim:
To assess the association of the CYBA, NOS3, and MTHFR gene polymorphisms and a rate of fibrosis progression in chronic hepatitis C (CHC).
Subjects And Methods:
One hundred and nine CHC patients with the verified stage of liver fibrosis and cirrhosis at its onset were examined. The disease duration was determined in all the patients and additional risk factors of liver lesion were absent. A group of rapidly progressive fibrosis comprised 55 patients with a calculated fibrosis progression rate of 0.130 fibrosis units/year or higher and 54 patients with a progression rate of less than 0.130 fibrosis units/year were assigned to a slow fibrosis group. A compression group consisted of 299 healthy blood donors. The polymorphism of the genes under study was determined by polymerase chain reaction-restriction fragment length polymorphism analysis.
Results:
The mutant TT genotype of the CYBA gene was significantly more common in the CHC patients with rapidly progressive fibrosis than in those with slowly progressive fibrosis (odds ratio for TT 9.09 at 95% confidence interval, 1.09 to 74.83; p = 0.0161). No significant differences were found in the distribution of the alleles and genotypes of the NOS3 and MTHFR genes between the groups of patients with slowly and rapidly progressive fibrosis.
Conclusion:
The findings make it possible to regard the TT genotype of the CYBA gene from the C242T locus as profibrogenic and as one of the markers of the poor course of CHC.
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