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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Hepatitis C virus infection and chronic kidney disease: Time for reappraisal
Patrice Cacoub1, Anne Claire Desbois1, Corinne Isnard-Bagnis2
1Sorbonne Universités, UPMC Université Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75005 Paris, France; INSERM, UMR_S 959, F-75013 Paris, France; CNRS, FRE3632, F-75005 Paris, France; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, F-75013 Paris, France.
Insights
Hepatitis C virus (HCV) infection significantly increases the risk of chronic kidney disease (CKD) and mortality in dialysis patients. New interferon-free treatments offer a safe and effective way to cure HCV in CKD patients.
Area of Science:
- Nephrology
- Hepatology
- Virology
Background:
- Hepatitis C virus (HCV) infection is a major cause of liver disease and is linked to significant extrahepatic manifestations, including chronic kidney disease (CKD).
- HCV infection is prevalent in dialysis patients and associated with increased mortality and poorer outcomes after kidney transplantation.
- Previous interferon-based treatments for HCV were often ineffective and poorly tolerated in CKD patients, limiting treatment uptake.
Purpose of the Study:
- To review the association between HCV and CKD.
- To discuss the impact of HCV on CKD prognosis.
- To evaluate the emerging role of direct-acting antiviral (DAA) therapies in managing HCV in patients with renal impairment.
Main Methods:
- Literature review of studies investigating HCV and CKD.
- Analysis of HCV prevalence, incidence, and mortality in CKD populations.
- Assessment of DAA efficacy and safety profiles in different stages of renal impairment.
Main Results:
- HCV infection is strongly associated with CKD, including an increased incidence of CKD and proteinuria, and is a cause of glomerulonephritis.
- HCV seropositivity in dialysis patients correlates with higher all-cause and cardiovascular mortality and reduced graft survival post-transplant.
- New interferon-free DAAs demonstrate high cure rates and a favorable safety profile in HCV patients with varying degrees of kidney function, with specific regimens recommended based on GFR.
Conclusions:
- HCV poses a significant threat to kidney health and overall survival in CKD patients.
- The advent of DAAs has revolutionized HCV treatment, offering curative options with good safety for CKD patients.
- Further research is needed to optimize DAA use in larger cohorts of HCV patients with renal impairment.
Abstract:
Hepatitis C virus (HCV) infection is associated with tremendous morbidity and mortality due to liver complications. HCV infection is also associated with many extrahepatic manifestations including cardiovascular diseases, glucose metabolism impairment, cryoglobulinemia vasculitis, B cell non-Hodgkin lymphoma and chronic kidney disease (CKD). Many studies have shown a strong association between HCV and CKD, by reporting (i) an increased prevalence of HCV infection in patients on haemodialysis, (ii) an increased incidence of CKD and proteinuria in HCV-infected patients, and (iii) the development of membranoproliferative glomerulonephritis secondary to HCV-induced cryoglobulinemia vasculitis. HCV seropositivity is found to be associated with an increased relative risk for all-cause and cardiovascular mortality in the dialysis population. HCV seropositivity is linked to lower patient and graft survival after kidney transplantation. Such poor HCV-associated prognosis should have encouraged clinicians to treat HCV in CKD patients. However, due to frequent side effects and the poor efficacy of interferon-based treatments, very few HCV dialysis patients have received HCV medications until now. The emergence of new direct acting, interferon-free antiviral treatment, leading to HCV cure in most cases with a satisfactory safety profile, will shortly modify the management of HCV infection in CKD patients. In patients with a glomerular filtration rate (GFR) >30ml/min, the choice of DAA is not restricted. In those with a GFR <30 and >15ml/min, only paritaprevir/ritonavir/ombitasvir/dasabuvir or a grazoprevir plus elbasvir regimen are approved. In patients with end stage renal disease (GFR <15ml/min or dialysis), current data only allows for the use of a grazoprevir plus elbasvir combination. No doubt these data will be modified in the future with the advent of new studies including larger cohorts of HCV patients with renal impairment.
Related Concept Videos
Chronic Kidney Disease I: Introduction
Chronic Kidney Disease II: Clinical Manifestations
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Chronic Kidney Disease III: Interprofessional Care
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Acute Kidney Injury IV: Diagnostic Studies and Prevention

