Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence
- Autores
- Fabrizi, Fabrizio; Cerutti, Roberta; Porata, Giulia; Messa, Piergiorgio; Ridruejo, Ezequiel
- Año de publicación
- 2019
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- 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.
Fil: Fabrizi, Fabrizio. No especifíca;
Fil: Cerutti, Roberta. No especifíca;
Fil: Porata, Giulia. No especifíca;
Fil: Messa, Piergiorgio. Università degli Studi di Milano; Italia
Fil: Ridruejo, Ezequiel. Universidad Austral. Hospital Universitario Austral; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina - Materia
-
DIRECT-ACTING ANTIVIRAL AGENTS
GLOMERULONEPHRITIS
HEPATITIS C CRYOGLOBULINEMIA
PROTEINURIA
SUSTAINED VIROLOGICAL RESPONSE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/147914
Ver los metadatos del registro completo
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CONICET Digital (CONICET) |
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Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidenceFabrizi, FabrizioCerutti, RobertaPorata, GiuliaMessa, PiergiorgioRidruejo, EzequielDIRECT-ACTING ANTIVIRAL AGENTSGLOMERULONEPHRITISHEPATITIS C CRYOGLOBULINEMIAPROTEINURIASUSTAINED VIROLOGICAL RESPONSEhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Glomerular 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.Fil: Fabrizi, Fabrizio. No especifíca;Fil: Cerutti, Roberta. No especifíca;Fil: Porata, Giulia. No especifíca;Fil: Messa, Piergiorgio. Università degli Studi di Milano; ItaliaFil: Ridruejo, Ezequiel. Universidad Austral. Hospital Universitario Austral; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; ArgentinaMolecular Diversity Preservation International2019-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/147914Fabrizi, Fabrizio; Cerutti, Roberta; Porata, Giulia; Messa, Piergiorgio; Ridruejo, Ezequiel; Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence; Molecular Diversity Preservation International; Pathogens; 8; 4; 10-2019; 1-122076-0817CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2076-0817/8/4/176info:eu-repo/semantics/altIdentifier/doi/10.3390/pathogens8040176info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:03:29Zoai:ri.conicet.gov.ar:11336/147914instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:03:29.704CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
title |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
spellingShingle |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence Fabrizi, Fabrizio DIRECT-ACTING ANTIVIRAL AGENTS GLOMERULONEPHRITIS HEPATITIS C CRYOGLOBULINEMIA PROTEINURIA SUSTAINED VIROLOGICAL RESPONSE |
title_short |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
title_full |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
title_fullStr |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
title_full_unstemmed |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
title_sort |
Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence |
dc.creator.none.fl_str_mv |
Fabrizi, Fabrizio Cerutti, Roberta Porata, Giulia Messa, Piergiorgio Ridruejo, Ezequiel |
author |
Fabrizi, Fabrizio |
author_facet |
Fabrizi, Fabrizio Cerutti, Roberta Porata, Giulia Messa, Piergiorgio Ridruejo, Ezequiel |
author_role |
author |
author2 |
Cerutti, Roberta Porata, Giulia Messa, Piergiorgio Ridruejo, Ezequiel |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
DIRECT-ACTING ANTIVIRAL AGENTS GLOMERULONEPHRITIS HEPATITIS C CRYOGLOBULINEMIA PROTEINURIA SUSTAINED VIROLOGICAL RESPONSE |
topic |
DIRECT-ACTING ANTIVIRAL AGENTS GLOMERULONEPHRITIS HEPATITIS C CRYOGLOBULINEMIA PROTEINURIA SUSTAINED VIROLOGICAL RESPONSE |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
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. Fil: Fabrizi, Fabrizio. No especifíca; Fil: Cerutti, Roberta. No especifíca; Fil: Porata, Giulia. No especifíca; Fil: Messa, Piergiorgio. Università degli Studi di Milano; Italia Fil: Ridruejo, Ezequiel. Universidad Austral. Hospital Universitario Austral; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina |
description |
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. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/147914 Fabrizi, Fabrizio; Cerutti, Roberta; Porata, Giulia; Messa, Piergiorgio; Ridruejo, Ezequiel; Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence; Molecular Diversity Preservation International; Pathogens; 8; 4; 10-2019; 1-12 2076-0817 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/147914 |
identifier_str_mv |
Fabrizi, Fabrizio; Cerutti, Roberta; Porata, Giulia; Messa, Piergiorgio; Ridruejo, Ezequiel; Direct-acting antiviral agents for HCV-associated glomerular disease and the current evidence; Molecular Diversity Preservation International; Pathogens; 8; 4; 10-2019; 1-12 2076-0817 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2076-0817/8/4/176 info:eu-repo/semantics/altIdentifier/doi/10.3390/pathogens8040176 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Molecular Diversity Preservation International |
publisher.none.fl_str_mv |
Molecular Diversity Preservation International |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269803076648960 |
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13.13397 |