Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783644250752155648 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7844021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mccaffreyjames bkvirusinfectionandoutcomefollowingkidneytransplantationinchildhood AT bhutevijeshj bkvirusinfectionandoutcomefollowingkidneytransplantationinchildhood AT shenoymohan bkvirusinfectionandoutcomefollowingkidneytransplantationinchildhood |