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Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients

INTRODUCTION: Currently, there is no specific immunosuppressive protocol for hepatitis C (HCV)-positive renal transplants recipients. Thus, the aim of this study was to evaluate the conversion effect to everolimus (EVR) on HCV in adult kidney recipients. METHOD: This is an exploratory single-center,...

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Autores principales: Pacheco, Larissa Sgaria, Garcia, Valter Duro, Prá, Ronivan Luis Dal, Cardoso, Bruna Doleys, Rodrigues, Mariana Ferras, Zanetti, Helen Kris, Meinerz, Gisele, Neumann, Jorge, Gnatta, Diego, Keitel, Elizete
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Nefrologia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533980/
https://www.ncbi.nlm.nih.gov/pubmed/29771270
http://dx.doi.org/10.1590/2175-8239-JBN-3860
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author Pacheco, Larissa Sgaria
Garcia, Valter Duro
Prá, Ronivan Luis Dal
Cardoso, Bruna Doleys
Rodrigues, Mariana Ferras
Zanetti, Helen Kris
Meinerz, Gisele
Neumann, Jorge
Gnatta, Diego
Keitel, Elizete
author_facet Pacheco, Larissa Sgaria
Garcia, Valter Duro
Prá, Ronivan Luis Dal
Cardoso, Bruna Doleys
Rodrigues, Mariana Ferras
Zanetti, Helen Kris
Meinerz, Gisele
Neumann, Jorge
Gnatta, Diego
Keitel, Elizete
author_sort Pacheco, Larissa Sgaria
collection PubMed
description INTRODUCTION: Currently, there is no specific immunosuppressive protocol for hepatitis C (HCV)-positive renal transplants recipients. Thus, the aim of this study was to evaluate the conversion effect to everolimus (EVR) on HCV in adult kidney recipients. METHOD: This is an exploratory single-center, prospective, randomized, open label controlled trial with renal allograft recipients with HCV-positive serology. Participants were randomized for conversion to EVR or maintenance of calcineurin inhibitors. RESULTS: Thirty patients were randomized and 28 were followed-up for 12 months (conversion group, Group 1 =15 and control group, Group 2 =13). RT-PCR HCV levels reported in log values were comparable in both groups and among patients in the same group. The statistical analysis showed no interaction effect between time and group (p value G*M= 0.852), overtime intra-groups (p-value M=0.889) and between group (p-value G=0.286). Group 1 showed a higher incidence of dyslipidemia (p=0.03) and proteinuria events (p=0.01), while no difference was observed in the incidence of anemia (p=0.17), new onset of post-transplant diabetes mellitus (p=1.00) or urinary tract infection (p=0.60). The mean eGFR was similar in both groups. CONCLUSION: Our study did not show viral load decrease after conversion to EVR with maintenance of antiproliferative therapy.
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spelling pubmed-65339802019-06-17 Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients Pacheco, Larissa Sgaria Garcia, Valter Duro Prá, Ronivan Luis Dal Cardoso, Bruna Doleys Rodrigues, Mariana Ferras Zanetti, Helen Kris Meinerz, Gisele Neumann, Jorge Gnatta, Diego Keitel, Elizete J Bras Nefrol Original Articles INTRODUCTION: Currently, there is no specific immunosuppressive protocol for hepatitis C (HCV)-positive renal transplants recipients. Thus, the aim of this study was to evaluate the conversion effect to everolimus (EVR) on HCV in adult kidney recipients. METHOD: This is an exploratory single-center, prospective, randomized, open label controlled trial with renal allograft recipients with HCV-positive serology. Participants were randomized for conversion to EVR or maintenance of calcineurin inhibitors. RESULTS: Thirty patients were randomized and 28 were followed-up for 12 months (conversion group, Group 1 =15 and control group, Group 2 =13). RT-PCR HCV levels reported in log values were comparable in both groups and among patients in the same group. The statistical analysis showed no interaction effect between time and group (p value G*M= 0.852), overtime intra-groups (p-value M=0.889) and between group (p-value G=0.286). Group 1 showed a higher incidence of dyslipidemia (p=0.03) and proteinuria events (p=0.01), while no difference was observed in the incidence of anemia (p=0.17), new onset of post-transplant diabetes mellitus (p=1.00) or urinary tract infection (p=0.60). The mean eGFR was similar in both groups. CONCLUSION: Our study did not show viral load decrease after conversion to EVR with maintenance of antiproliferative therapy. Sociedade Brasileira de Nefrologia 2018-05-14 2018 /pmc/articles/PMC6533980/ /pubmed/29771270 http://dx.doi.org/10.1590/2175-8239-JBN-3860 Text en https://creativecommons.org/licenses/by/4.0/ 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 Original Articles
Pacheco, Larissa Sgaria
Garcia, Valter Duro
Prá, Ronivan Luis Dal
Cardoso, Bruna Doleys
Rodrigues, Mariana Ferras
Zanetti, Helen Kris
Meinerz, Gisele
Neumann, Jorge
Gnatta, Diego
Keitel, Elizete
Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title_full Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title_fullStr Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title_full_unstemmed Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title_short Effect of conversion from calcineurin inhibitors to everolimus on hepatitis C viremia in adult kidney transplant recipients
title_sort effect of conversion from calcineurin inhibitors to everolimus on hepatitis c viremia in adult kidney transplant recipients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533980/
https://www.ncbi.nlm.nih.gov/pubmed/29771270
http://dx.doi.org/10.1590/2175-8239-JBN-3860
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