Abstract

Glomerular disease is an extra-hepatic manifestation of hepatitis C virus infection (HCV) and membranoproliferative glomerulonephritis is the most frequent glomerular disease associated with HCV. It occurs commonly in patients with HCV-related mixed cryoglobulinemia syndrome. Patients with HCV-related glomerular disease have been historically a difficult-to-treat group. The therapeutic armamentarium for HCV-related glomerular disease now includes antiviral regimens, selective or non-specific immunosuppressive drugs, immunomodulators, and symptomatic agents. The treatment of HCV-associated glomerular disease is dependent on the clinical presentation of the patient. The recent introduction of all-oral, interferon (IFN)-free/ribavirin (RBV)-free regimens is dramatically changing the course of HCV in the general population, and some regimens have been approved for HCV even in patients with advanced chronic kidney disease. According to a systematic review of the medical literature, the evidence concerning the efficacy/safety of direct-acting antiviral agents (DAAs) of HCV-induced glomerular disease is limited. The frequency of sustained virological response was 92.5% (62/67). Full or partial clinical remission was demonstrated in many patients (n = 46, 68.5%) after DAAs. There were no reports of deterioration of kidney function in patients on DAAs. Many patients (n = 29, 43%) underwent immunosuppression while on DAAs. A few cases of new onset or relapsing glomerular disease in patients with HCV successfully treated with DAAs have been observed. In summary, DAA-based combinations are making easier the management of HCV. However, patients with HCV-induced glomerular disease are still a difficult-to-treat group even at the time of DAAs.

Highlights

  • More than 71 million people have chronic hepatitis C virus (HCV) infection worldwide

  • HCV infection is the main cause of mixed cryoglobulinemia, a systemic vasculitis producing various clinical manifestations which range from the so-called MCS to important abnormalities including neurological and renal diseases [1,2]

  • (1) Antiviral therapy has been given with the idea that the underlying infection promotes the synthesis of immune complexes and resultant glomerular disease; (2) Nonspecific immunosuppressive agents lowering glomerular inflammation have been adopted by several authors; (3) An additional choice is given by rituximab (RTX), which selectively targets B cells and causes depletion of B cells

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Summary

Introduction

More than 71 million people have chronic hepatitis C virus (HCV) infection worldwide. HCV infection is the main cause of mixed cryoglobulinemia, a systemic vasculitis producing various clinical manifestations which range from the so-called MCS (purpura, asthenia, and arthralgias) to important abnormalities including neurological and renal diseases [1,2]. HCV-MCS is more frequent in women than men and affects patients with cirrhosis more commonly than chronic hepatitis. It appears that HCV-MCS is not affected by HCV genotype, viral load, or duration of HCV infection [1,2]. Renal disease is considered an important cause of morbidity and mortality in MC vasculitis induced by HCV [3]. The purpose of this review is to report the most important data concerning the treatment of HCV-related glomerular disease, an important extra-hepatic complication of HCV infection

HCV-Associated Kidney Disease
HCV and Kidney-Updated Evidence
Treatment of HCV-Related Glomerular Disease
Antiviral Treatment
Antiviral
Immunosuppressive Agents for Treatment of HCV-Related Glomerular Disease
Rituximab for Treatment of HCV-Related Glomerular Disease
Non-Selective Immunosuppression for HCV-Related Glomerular Disease
Findings
10. Conclusions
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