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MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes

Abstract. Introduction: The association of hepatitis C virus (HCV), cryoglobulinemia, and membranoproliferative glomerulonephritis (MPGN) is well known. Treatment of underlying HCV infection has greatly improved in recent years with the introduction of direct-acting antivirals (DAA), which have demo...

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Autores principales: Palombo, Shannon B., Wendel, Eric C., Kidd, Laura R., Yazdi, Farshid, Naljayan, Mihran V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663211/
https://www.ncbi.nlm.nih.gov/pubmed/29098140
http://dx.doi.org/10.5414/CNCS109099
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author Palombo, Shannon B.
Wendel, Eric C.
Kidd, Laura R.
Yazdi, Farshid
Naljayan, Mihran V.
author_facet Palombo, Shannon B.
Wendel, Eric C.
Kidd, Laura R.
Yazdi, Farshid
Naljayan, Mihran V.
author_sort Palombo, Shannon B.
collection PubMed
description Abstract. Introduction: The association of hepatitis C virus (HCV), cryoglobulinemia, and membranoproliferative glomerulonephritis (MPGN) is well known. Treatment of underlying HCV infection has greatly improved in recent years with the introduction of direct-acting antivirals (DAA), which have demonstrated curative sustained viral response (SVR) rates for select viral genotypes with the added benefit of less drug side effects. However, a mainstay of newer DAAs is sofosbuvir, which is contraindicated in patients with severe renal impairment. Case history: We are reporting the case of a 65-year-old female with chronic systolic heart failure, hypertension, and chronic HCV genotype 1b with biopsy-proven type I MPGN with cryoglobulinemia type II, who presented with rapidly progressive renal failure requiring emergent hemodialysis. After initiation of DAA therapy including ombitasvir-paritaprevir-ritonavir plus dasabuvir, in conjunction with plasmapheresis, corticosteroids, and rituximab, there was significant improvement in renal function such that hemodialysis was no longer needed. Discussion: This patient’s HCV treatment is estimated to induce a greater than 90% SVR, which is notably promising for the reduction and/or reversal of HCV-related glomerulopathy. Most recent HCV guidelines from 2015 recommend this regimen; however, there is little data to evaluate the safety and efficacy of treatment. Therefore, it is valuable to report positive preliminary results at this time. Overall, we anticipate this treatment regimen to become a basis in the management of HCV-related renal disease; however, larger studies will still be needed to prove its efficacy in improving renal outcomes.
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spelling pubmed-56632112017-11-02 MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes Palombo, Shannon B. Wendel, Eric C. Kidd, Laura R. Yazdi, Farshid Naljayan, Mihran V. Clin Nephrol Case Stud Case Report Abstract. Introduction: The association of hepatitis C virus (HCV), cryoglobulinemia, and membranoproliferative glomerulonephritis (MPGN) is well known. Treatment of underlying HCV infection has greatly improved in recent years with the introduction of direct-acting antivirals (DAA), which have demonstrated curative sustained viral response (SVR) rates for select viral genotypes with the added benefit of less drug side effects. However, a mainstay of newer DAAs is sofosbuvir, which is contraindicated in patients with severe renal impairment. Case history: We are reporting the case of a 65-year-old female with chronic systolic heart failure, hypertension, and chronic HCV genotype 1b with biopsy-proven type I MPGN with cryoglobulinemia type II, who presented with rapidly progressive renal failure requiring emergent hemodialysis. After initiation of DAA therapy including ombitasvir-paritaprevir-ritonavir plus dasabuvir, in conjunction with plasmapheresis, corticosteroids, and rituximab, there was significant improvement in renal function such that hemodialysis was no longer needed. Discussion: This patient’s HCV treatment is estimated to induce a greater than 90% SVR, which is notably promising for the reduction and/or reversal of HCV-related glomerulopathy. Most recent HCV guidelines from 2015 recommend this regimen; however, there is little data to evaluate the safety and efficacy of treatment. Therefore, it is valuable to report positive preliminary results at this time. Overall, we anticipate this treatment regimen to become a basis in the management of HCV-related renal disease; however, larger studies will still be needed to prove its efficacy in improving renal outcomes. Dustri-Verlag Dr. Karl Feistle 2017-10-23 /pmc/articles/PMC5663211/ /pubmed/29098140 http://dx.doi.org/10.5414/CNCS109099 Text en © Dustri-Verlag Dr. K. Feistle http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Palombo, Shannon B.
Wendel, Eric C.
Kidd, Laura R.
Yazdi, Farshid
Naljayan, Mihran V.
MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title_full MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title_fullStr MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title_full_unstemmed MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title_short MPGN and mixed cryoglobulinemia in a patient with hepatitis C – new treatment implications and renal outcomes
title_sort mpgn and mixed cryoglobulinemia in a patient with hepatitis c – new treatment implications and renal outcomes
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663211/
https://www.ncbi.nlm.nih.gov/pubmed/29098140
http://dx.doi.org/10.5414/CNCS109099
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