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Published on: April 19, 2024
Effect of interferon-alpha-based antiviral therapy on hepatitis C virus-associated glomerulonephritis: a
Bo Feng1, Garabed Eknoyan, Zhong-Sheng Guo
1Hepatology Institute, Peking University People's Hospital, Beijing, China.
Insights
Interferon-alfa (IFN-α) antiviral therapy significantly reduces proteinuria and stabilizes serum creatinine in patients with Hepatitis C virus (HCV)-associated glomerulonephritis. Achieving viral clearance further enhances these beneficial effects on kidney function.
Area of Science:
- Nephrology
- Hepatology
- Virology
Background:
- Hepatitis C virus (HCV) is linked to various glomerulopathies, causing kidney function decline.
- The impact of antiviral treatments on HCV-associated kidney disease progression remains debated.
- This study systematically analyzes interferon (IFN)-α-based therapy's effect on HCV-associated chronic kidney disease.
Purpose of the Study:
- To evaluate the efficacy of interferon (IFN)-α-based antiviral therapy in patients with HCV-associated glomerulonephritis.
- To assess the impact of this therapy on proteinuria and serum creatinine levels.
- To determine if sustained virological response influences kidney function improvement.
Main Methods:
- A meta-analysis of controlled and uncontrolled clinical trials was conducted.
- Studies focused on IFN-α-based antiviral therapy for HCV-associated glomerulonephritis.
- Key endpoints included improvements in proteinuria and serum creatinine levels.
Main Results:
- Eleven trials with 225 patients showed a significant decrease in proteinuria (2.71 g/24 h) and serum creatinine (0.23 mg/dL) post-therapy.
- Patients achieving sustained virological response (SVR) exhibited a greater reduction in proteinuria compared to non-SVR groups.
- No significant difference in serum creatinine decrease was observed between SVR and non-SVR groups.
Conclusions:
- Interferon-alfa (IFN-α)-based antiviral therapy is effective in reducing proteinuria and stabilizing serum creatinine in HCV-associated glomerulonephritis.
- The therapy should be considered for patients with this condition.
- Greater proteinuria improvement in patients with HCV RNA clearance supports a causal role of HCV in glomerulonephritis.
Background:
Hepatitis C virus (HCV) is associated with various glomerulopathies, in which HCV is responsible not only for the onset of glomerulopathy but also for its progressive loss of kidney function. The effect of antiviral treatment on the glomerular lesions and subsequent course of kidney disease remains controversial. Therefore, we performed a systematic analysis of the available evidence on the effect of interferon (IFN)-α-based therapy on HCV-associated chronic kidney disease.
Methods:
A meta-analysis was performed of controlled and uncontrolled clinical studies related to IFNα-based antiviral therapy and its impact on kidney function in HCV-associated glomerulonephritis. Improvement of proteinuria and serum creatinine levels after antiviral therapy was taken as the end points of interest. Data from eligible studies selected according to protocols were analysed using Review Manager 5.0.
Results:
Eleven clinical trials involving 225 patients were included in our meta-analysis. At the end of antiviral therapy, the summary estimate of the mean decrease in proteinuria was 2.71 g/24 h [95% confidence interval (CI) 1.38-4.04, P < 0.0001], P-value for heterogeneity 0.05 (I(2) = 53%). The pooled decrease in mean serum creatinine levels was 0.23 mg/dL (95% CI 0.02-0.44, P = 0.03), P-value for heterogeneity 0.30 (I(2) = 17%). Comparison of non-sustained virological response (SVR) to SVR groups demonstrated a mean difference of proteinuria decrease in the SVR group of 1.04 g/24 h (95% CI 0.20-1.89, P = 0.02), P-value for heterogeneity 0.21 (I(2) = 36%) and of serum creatinine decrease of 0.05 mg/dL (95% CI -0.33 to 0.43, P = 0.80), P-value for heterogeneity 0.70 (I(2) = 0%).
Conclusion:
Antiviral therapy based on IFNα can significantly decrease proteinuria and stabilize serum creatitine, and therefore, should be undertaken in patients with HCV-associated glomerulonephritis. The improvement in protein excretion is greater in those who achieve HCV RNA clearance, a finding in line with a causal role for HCV in glomerulonephritis.
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