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BK virus infection and outcome following kidney transplantation in childhood

BK virus associated nephropathy (BKN) is an important cause of kidney allograft failure. In a cohort of paediatric kidney transplant recipients, we aimed to understand the incidence and clinical outcome associated with BKN, as well as identify risk factors for BKN and BK viraemia development. We ret...

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Autores principales: McCaffrey, James, Bhute, Vijesh J., Shenoy, Mohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844021/
https://www.ncbi.nlm.nih.gov/pubmed/33510329
http://dx.doi.org/10.1038/s41598-021-82160-0
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author McCaffrey, James
Bhute, Vijesh J.
Shenoy, Mohan
author_facet McCaffrey, James
Bhute, Vijesh J.
Shenoy, Mohan
author_sort McCaffrey, James
collection PubMed
description BK virus associated nephropathy (BKN) is an important cause of kidney allograft failure. In a cohort of paediatric kidney transplant recipients, we aimed to understand the incidence and clinical outcome associated with BKN, as well as identify risk factors for BKN and BK viraemia development. We retrospectively analysed all patients who received a kidney transplant and received follow up care in our centre between 2009–2019. Among 106 patients included in the study (mean follow up 4.5 years), 32/106 (30.2%) patients experienced BK viraemia. The incidence of BKN was 7/106 (6.6%). The median time of BK viraemia development post-transplant was 279.5 days compared to 90.0 days for BKN. Development of BKN was associated with younger age at transplantation (p = 0.013). Development of BK viraemia was associated with negative recipient serology for cytomegalovirus (CMV) at time of transplantation (p = 0.012) and a higher net level of immunosuppression (p = 0.039). There was no difference in graft function at latest follow up between those who experienced BKN and those without BKN. This study demonstrates that BK virus infection is associated with younger age at transplantation, CMV negative recipient serostatus and higher levels of immunosuppression. Judicious monitoring of BK viraemia in paediatric transplant recipients, coupled with timely clinical intervention can result in similar long-term outcomes for BKN patients compared to controls.
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spelling pubmed-78440212021-01-29 BK virus infection and outcome following kidney transplantation in childhood McCaffrey, James Bhute, Vijesh J. Shenoy, Mohan Sci Rep Article BK virus associated nephropathy (BKN) is an important cause of kidney allograft failure. In a cohort of paediatric kidney transplant recipients, we aimed to understand the incidence and clinical outcome associated with BKN, as well as identify risk factors for BKN and BK viraemia development. We retrospectively analysed all patients who received a kidney transplant and received follow up care in our centre between 2009–2019. Among 106 patients included in the study (mean follow up 4.5 years), 32/106 (30.2%) patients experienced BK viraemia. The incidence of BKN was 7/106 (6.6%). The median time of BK viraemia development post-transplant was 279.5 days compared to 90.0 days for BKN. Development of BKN was associated with younger age at transplantation (p = 0.013). Development of BK viraemia was associated with negative recipient serology for cytomegalovirus (CMV) at time of transplantation (p = 0.012) and a higher net level of immunosuppression (p = 0.039). There was no difference in graft function at latest follow up between those who experienced BKN and those without BKN. This study demonstrates that BK virus infection is associated with younger age at transplantation, CMV negative recipient serostatus and higher levels of immunosuppression. Judicious monitoring of BK viraemia in paediatric transplant recipients, coupled with timely clinical intervention can result in similar long-term outcomes for BKN patients compared to controls. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7844021/ /pubmed/33510329 http://dx.doi.org/10.1038/s41598-021-82160-0 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
McCaffrey, James
Bhute, Vijesh J.
Shenoy, Mohan
BK virus infection and outcome following kidney transplantation in childhood
title BK virus infection and outcome following kidney transplantation in childhood
title_full BK virus infection and outcome following kidney transplantation in childhood
title_fullStr BK virus infection and outcome following kidney transplantation in childhood
title_full_unstemmed BK virus infection and outcome following kidney transplantation in childhood
title_short BK virus infection and outcome following kidney transplantation in childhood
title_sort bk virus infection and outcome following kidney transplantation in childhood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844021/
https://www.ncbi.nlm.nih.gov/pubmed/33510329
http://dx.doi.org/10.1038/s41598-021-82160-0
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