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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
HCV and the kidney
Marion Corouge1,2, Anaïs Vallet-Pichard1,2, Stanislas Pol1,2
1Hepatology Department, Université Paris Descartes, Cochin Hospital, APHP, Paris, France.
Insights
Chronic hepatitis C (CHC) significantly harms kidney function, increasing mortality in dialysis patients. Oral antiviral therapies, like direct-acting antivirals (DAAs), offer excellent outcomes for CHC patients with advanced chronic kidney disease.
Area of Science:
- Nephrology
- Hepatology
- Virology
Background:
- Chronic hepatitis C (CHC) is linked to progressive renal deterioration.
- Advanced chronic kidney disease (CKD) exacerbates hepatitis C virus (HCV) infection and impacts liver health, transplantation outcomes, and patient survival.
- HCV-infected dialysis patients face higher mortality rates compared to uninfected patients or HCV-infected kidney recipients.
Purpose of the Study:
- To highlight the critical association between CHC and renal impairment.
- To emphasize the necessity of oral antiviral treatments for CKD patients with HCV.
- To advocate for prioritized treatment access for specific CKD patient groups.
Main Methods:
- Review of existing literature on CHC, CKD, and HCV outcomes.
- Analysis of mortality data comparing different patient cohorts (dialysis, kidney recipients).
- Evaluation of current treatment guidelines and outcomes for direct-acting antiviral (DAA) therapies in CKD.
Main Results:
- Renal impairment, particularly stage 4-5 CKD, increases HCV prevalence and negatively affects liver health and transplant outcomes.
- HCV-infected dialysis patients exhibit significantly higher mortality.
- DAA treatment in late-stage CKD patients demonstrates excellent efficacy, comparable to the general population.
Conclusions:
- Oral antiviral therapies are crucial for managing HCV in patients with CKD.
- Patients with stage 4-5 CKD, including dialysis patients and kidney recipients, require prioritized access to DAAs.
- Further research is needed to refine DAA treatment protocols for CKD patients, focusing on dosage adjustments and drug interactions.
Abstract:
Chronic hepatitis C (CHC) is significantly associated with a risk of renal deterioration over time. Renal impairment, especially stage 4-5 chronic kidney disease, increases the risk of: (i) the prevalence and incidence (in dialysis/transplantation) of hepatitis C virus (HCV) infection; (ii) liver deterioration during kidney transplantation and (iii) allograft failure and patient mortality. HCV-infected dialysis patients have a higher mortality than non-infected dialysis patients and than HCV-infected kidney recipients. The harmful impact of HCV emphasizes the need for oral antiviral therapies in patients with chronic kidney disease. Symptomatic cryoglobulinemic vasculitis and extensive liver fibrosis are already approved indications for early access to oral antiviral treatment. Patients with stage 4-5 chronic kidney disease should also be given priority: dialysis patients (whatever the stage of fibrosis and whether or not they are candidates for kidney transplantation) as well as all kidney recipients. The results of treatment of HCV with direct-acting antiviral (DAAs) drugs in patients with late chronic kidney disease are excellent, similar to those in the general population, although additional clinical trials are definitely needed, particularly to optimize adjustment of treatment to kidney function and determine the risk of drug-drug interactions.
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