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Meta-analysis of combined therapy for adult hepatitis B virus-associated glomerulonephritis
Xiao-Yong Zheng1, Ri-Bao Wei, Li Tang
1Department of Nephrology, General Hospital of Chinese PLA, Beijing 100853, China.
Insights
Combined antiviral and immunosuppressant therapy effectively treats hepatitis B virus-associated glomerulonephritis (HBV-GN) by reducing proteinuria and improving albumin levels. This approach is safe, showing no significant impact on viral replication or organ function in adult patients.
Area of Science:
- Nephrology
- Hepatology
- Immunology
Background:
- Hepatitis B virus-associated glomerulonephritis (HBV-GN) is a significant cause of kidney disease in endemic areas.
- Optimal treatment strategies for HBV-GN remain under investigation, balancing viral suppression with immunosuppression.
Purpose of the Study:
- To evaluate the efficacy and safety of combined antiviral and immunosuppressant therapy in adult patients with HBV-GN.
- To assess the impact of this combined therapy on proteinuria, serological markers, and renal function.
Main Methods:
- A systematic literature search was conducted across multiple databases (PubMed, Embase, Cochrane, etc.) for studies published between 1980 and 2010.
- Meta-analysis of 12 clinical trials involving 317 adult HBV-GN patients treated with combined antiviral and immunosuppressant therapies.
- Outcomes included proteinuria remission, HBV e-antigen clearance, serum albumin, liver enzymes, creatinine, and HBV-DNA levels.
Main Results:
- Combined therapy significantly reduced proteinuria and increased serum albumin levels in HBV-GN patients.
- No significant adverse effects on liver or renal function were observed.
- HBV-DNA replication did not show significant activation, and no significant differences were found based on corticosteroid dosage or glomerulonephritis pathological type.
Conclusions:
- Combined antiviral and immunosuppressant therapy is an effective treatment for improving proteinuria in HBV-GN patients.
- This therapeutic approach demonstrates a favorable safety profile, without negatively impacting viral replication or organ function.
Aim:
To investigate the efficacy and safety of combined antiviral and immunosuppressant therapy in adult hepatitis B virus-associated glomerulonephritis (HBV-GN) patients.
Methods:
A computerized literature search was carried out in the PubMed database, Embase, the Cochrane Library, Chinese BioMedical Literature on disc, Chinese Medical Current Contents, Chinese National Knowledge Infrastructure, Wanfang and VIP (Chinese Technological Journal of Database) to collect articles between June 1980 and December 2010 on therapy with immunosuppressants, e.g., glucorticosteroids, mycophenolate mofetil and leflunomide, combined with antivirals, e.g., interferon, lamivudine, entecavir and adefovir dipivoxil, in adult HBV-GN patients. The primary outcomes were remission of proteinuria, clearance of HBV e-antigen, and elevation of serum albumin. The secondary outcomes were blood levels of alanine aminotransferase, serum creatinine, and HBV-DNA titer. Meta-analysis was performed using Review Manager 5.1. Fixed or random effect models were employed to combine the results after a heterogeneity test. The effects of the combined therapy were analyzed for different doses of glucorticosteroid and different types of HBV-GN.
Results:
Twelve clinical trials with 317 patients were included. A significantly higher incidence of HBV-GN was found in male patients (relative risk = 2.40, 95% CI: 1.98-2.93). Combined therapy reduced the proteinuria significantly with a mean difference of 4.19 (95% CI: 3.86-4.53) and increased the serum albumin concentration significantly with a mean difference of -11.95 (95% CI: -12.97-10.93) without significant alterations of liver function (mean difference: 4.62, 95% CI: -2.55-11.79) and renal function (mean difference: 10.29, 95% CI: 0.14-20.45). No significant activation of HBV-DNA replication occurred (mean difference: 0.12, 95% CI: -0.37-0.62). There was no significant difference between the high dose glucorticosteroid group and the low dose glucorticosteroid group in terms of proteinuria remission (P = 0.76) and between different pathological types of HBV-GN [membranous glomerulonephritis (MN) vs. mesangial proliferative glomerulonephritis, P = 0.68; MN vs membranoproliferative glomerulonephritis, P = 0.27].
Conclusion:
Combined antiviral and immunosuppressant therapy can improve the proteinuria in HBV-GN patients without altering HBV replication or damaging liver and renal functions.
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