PMID- 32129203 OWN - NLM STAT- MEDLINE DCOM- 20210111 LR - 20210111 IS - 1319-2442 (Print) IS - 1319-2442 (Linking) VI - 31 IP - 1 DP - 2020 Jan-Feb TI - Ribavirin as a beneficial treatment option for hepatitis C virusassociated glomerular disease. PG - 109-117 LID - 10.4103/1319-2442.279930 [doi] AB - The management of hepatitis C virus (HCV)-induced glomerular disease remains unsatisfactory despite novel advances in antiviral and immunosuppressive therapy. Recent evidence highlighted the role of ribavirin, a drug provided with immunomodulatory properties, in the treatment of glomerular diseases associated with chronic HCV. We administered low-dose ribavirin (200 mg/day or 200 mg twice a week or 200 mg thrice weekly) in a prospective fashion to a group of patients with HCV-associated glomerular disease (n = 7). Ribavirin monotherapy was given in most (n = 6) patients and was accompanied by erythropoietin therapy in all. The primary endpoint was reduction of 24-h proteinuria after treatment ended; the secondary end-points were decrease in serum creatinine and amelioration of urinary abnormalities. We collected data on on-treatment adverse events (AEs), serious AEs, and laboratory abnormalities. Many patients (n = 6) had inactive HCV infection as they had shown HCV RNA clearance from serum after antiviral therapy with direct-acting antivirals. Some patients (n = 4) had membranoproliferative glomerulo- nephritis, the diagnosis being confirmed by kidney histology in three cases; others (n = 2) received diagnosis of diabetic glomerulosclerosis, confirmed in one by kidney biopsy. We observed consistent reduction of 24-h proteinuria in two individuals after ribavirin therapy; another patient reported disappearance of microscopic hematuria. We found severe AE (hemolytic anemia) in three patients which required discontinuation of ribavirin treatment in two patients, one required hospitalization. Other AEs were cutaneous rash (n = 1), dyspepsia (n = 1), and fatigue (n = 1). Low-dose ribavirin was able to give consistent reduction of 24-h proteinuria in two patients; tolerance to ribavirin was unsatisfactory. We need further studies aimed to expand our knowledge on ribavirin therapy of HCV-associated glomerular disease. The low incidence of the disease hampers the conduction of clinical trials on this aim. FAU - Fabrizi, Fabrizio AU - Fabrizi F AD - Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Cresseri, Donata AU - Cresseri D AD - Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Moroni, Gabriella AU - Moroni G AD - Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Passerini, Patrizia AU - Passerini P AD - Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Pallotti, Francesco AU - Pallotti F AD - Division of Pathology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Donato, Francesca Maria AU - Donato FM AD - Division of Gastroenterology, Maggiore Hospital and IRCCS Foundation, Milano, Italy. FAU - Lampertico, Pietro AU - Lampertico P AD - Division of Gastroenterology, Maggiore Hospital and IRCCS Foundation; Deparment of Medicine, University School of Medicine, Milano, Italy. FAU - Messa, Piergiorgio AU - Messa P AD - Division of Nephrology, Maggiore Hospital and IRCCS Foundation; Deparment of Medicine, University School of Medicine, Milano, Italy. LA - eng PT - Journal Article PL - Saudi Arabia TA - Saudi J Kidney Dis Transpl JT - Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia JID - 9436968 RN - 0 (Antiviral Agents) RN - 49717AWG6K (Ribavirin) SB - IM MH - Aged MH - Antiviral Agents/adverse effects/*therapeutic use MH - Female MH - Hepatitis C, Chronic/complications/*drug therapy MH - Humans MH - Kidney Diseases/*drug therapy/virology MH - Male MH - Middle Aged MH - Prospective Studies MH - Ribavirin/adverse effects/*therapeutic use MH - Treatment Outcome EDAT- 2020/03/05 06:00 MHDA- 2021/01/12 06:00 CRDT- 2020/03/05 06:00 PHST- 2020/03/05 06:00 [entrez] PHST- 2020/03/05 06:00 [pubmed] PHST- 2021/01/12 06:00 [medline] AID - SaudiJKidneyDisTranspl_2020_31_1_109_279930 [pii] AID - 10.4103/1319-2442.279930 [doi] PST - ppublish SO - Saudi J Kidney Dis Transpl. 2020 Jan-Feb;31(1):109-117. doi: 10.4103/1319-2442.279930.