What is the relationship between Hepatitis and nephropathy (kidney disease)?

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Last updated: March 6, 2025 • View editorial policy

From the Guidelines

Hepatitis C infection is strongly associated with an increased risk of kidney disease, particularly in patients with chronic kidney disease (CKD) stage 4 or 5, and those on haemodialysis, and treatment with direct-acting antivirals such as glecaprevir/pibrentasvir is recommended to achieve viral clearance and potentially improve kidney function. The relationship between hepatitis and nephropathy is complex, with hepatitis C infection being a significant risk factor for the development of kidney disease, including glomerulonephritis and kidney failure. According to the EASL recommendations on treatment of hepatitis C 1, patients with CKD stage 4 or 5, including those on haemodialysis, should be treated with the fixed-dose combination of glecaprevir and pibrentasvir for 12 weeks, as it has been shown to be highly effective in achieving viral clearance, with an SVR12 rate of 98% in patients with CKD stage 4 or 5.

Some key points to consider in the management of hepatitis-associated nephropathy include:

  • The use of direct-acting antivirals such as sofosbuvir/velpatasvir or glecaprevir/pibrentasvir to achieve viral clearance
  • The importance of monitoring kidney function regularly through serum creatinine, estimated glomerular filtration rate, and urinalysis
  • The potential benefits of treating hepatitis C infection in patients with CKD, including the potential to improve kidney function and reduce the risk of kidney failure
  • The need to consider the optimal timing of treatment in patients on dialysis, including pre- or post-renal transplantation, and the potential risks and benefits of treatment in this population, as outlined in the KDIGO guideline on the prevention, diagnosis, evaluation, and treatment of hepatitis C virus infection in chronic kidney disease 2.

Overall, the treatment of hepatitis C infection in patients with kidney disease requires a comprehensive approach that takes into account the patient's underlying kidney function, the severity of their hepatitis C infection, and the potential risks and benefits of treatment. The use of direct-acting antivirals such as glecaprevir/pibrentasvir is a key component of this approach, and has been shown to be highly effective in achieving viral clearance and potentially improving kidney function.

From the Research

Relationship Between Hepatitis and Nephropathy

  • Hepatitis B virus (HBV) infection has been associated with the development of nephropathy, particularly membranous nephropathy [ 3, 4, 5, 6 ]
  • The underlying pathogenesis of hepatitis B-related glomerulonephritis (HBV-GN) involves immune complexes, which can be isolated from kidney tissues [ 3 ]
  • Clearance of HBV antigenemia improves renal impairment and proteinuria in HBV-GN patients [ 3, 6 ]

Treatment of Hepatitis B-Associated Nephropathy

  • Antiviral therapy is an effective treatment for HBV-associated nephropathy, with interferon and nucleoside analogs being equally effective at causing proteinuria remission and HBeAg clearance 4, 7, 5
  • Novel nucleoside analogues, such as entecavir, adefovir, and clevudine, can be effective for treatment of HBV-associated nephropathy, including lamivudine-resistant strains 5
  • Immunosuppression monotherapy, such as corticosteroids, is of little benefit and potentially harmful to HBV-GN patients due to the possibility of viral reactivation [ 3 ]

Clinical Outcomes

  • Complete remission of hepatitis B virus-associated nephrotic syndrome from IgA nephropathy has been reported following peginterferon therapy 7
  • Antiviral therapy has been shown to improve renal outcome in patients with hepatitis B virus-associated membranous nephropathy (HBV-MN) 4, 5, 6

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.