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Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients
BACKGROUND: The long-term prognosis of BK virus-associated nephropathy (BKVAN) in kidney transplant recipients (KTRs) is uncertain. We evaluated the long-term prognosis in KTRs with BKVAN and the clinical significance of BKVAN on post-transplant clinical outcome. METHODS: We retrospectively analyzed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Nephrology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027809/ https://www.ncbi.nlm.nih.gov/pubmed/29971212 http://dx.doi.org/10.23876/j.krcp.2018.37.2.167 |
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author | Park, Woo Yeong Kang, Seong Sik Jin, Kyubok Park, Sung Bae Choe, Misun Han, Seungyeup |
author_facet | Park, Woo Yeong Kang, Seong Sik Jin, Kyubok Park, Sung Bae Choe, Misun Han, Seungyeup |
author_sort | Park, Woo Yeong |
collection | PubMed |
description | BACKGROUND: The long-term prognosis of BK virus-associated nephropathy (BKVAN) in kidney transplant recipients (KTRs) is uncertain. We evaluated the long-term prognosis in KTRs with BKVAN and the clinical significance of BKVAN on post-transplant clinical outcome. METHODS: We retrospectively analyzed the medical records of 582 patients who underwent kidney transplant (KT) between 2001 and 2014. We divided the patients into a BKVAN group (15 patients) diagnosed by allograft biopsy and a control group (356 patients). RESULTS: The incidence of BKVAN was 4.0%, and the mean follow-up duration was 93.1 ± 52.3 months. Median time from KT to BKVAN diagnosis was 5.9 months (interquartile range [IQR], 4.4–8.7). In the BKVAN group, 9 (60.0%) KTRs with combined acute rejection progressed to graft failure, and the median time from BKVAN diagnosis to graft failure was 36.2 months (IQR, 9.7–65.5). Death-censored graft survival rate and patient survival rate in the BKVAN group were significantly lower than those in the control group. BKVAN and rejection were independent risk factors for graft failure. In the subgroup analysis, death-censored graft survival rate of KTRs with BKVAN with acute rejection was significantly worst in comparison with similar patients without BKVAN regardless of acute rejection (P < 0.001). CONCLUSION: The long-term prognosis of BKVAN with acute rejection was very poor because of graft failure caused by inadequate treatment for acute rejection considering BKVAN. Therefore, we should carefully monitor the allograft status of KTRs through regular surveillance tests after treatment for BKVAN with acute rejection. |
format | Online Article Text |
id | pubmed-6027809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society of Nephrology |
record_format | MEDLINE/PubMed |
spelling | pubmed-60278092018-07-03 Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients Park, Woo Yeong Kang, Seong Sik Jin, Kyubok Park, Sung Bae Choe, Misun Han, Seungyeup Kidney Res Clin Pract Original Article BACKGROUND: The long-term prognosis of BK virus-associated nephropathy (BKVAN) in kidney transplant recipients (KTRs) is uncertain. We evaluated the long-term prognosis in KTRs with BKVAN and the clinical significance of BKVAN on post-transplant clinical outcome. METHODS: We retrospectively analyzed the medical records of 582 patients who underwent kidney transplant (KT) between 2001 and 2014. We divided the patients into a BKVAN group (15 patients) diagnosed by allograft biopsy and a control group (356 patients). RESULTS: The incidence of BKVAN was 4.0%, and the mean follow-up duration was 93.1 ± 52.3 months. Median time from KT to BKVAN diagnosis was 5.9 months (interquartile range [IQR], 4.4–8.7). In the BKVAN group, 9 (60.0%) KTRs with combined acute rejection progressed to graft failure, and the median time from BKVAN diagnosis to graft failure was 36.2 months (IQR, 9.7–65.5). Death-censored graft survival rate and patient survival rate in the BKVAN group were significantly lower than those in the control group. BKVAN and rejection were independent risk factors for graft failure. In the subgroup analysis, death-censored graft survival rate of KTRs with BKVAN with acute rejection was significantly worst in comparison with similar patients without BKVAN regardless of acute rejection (P < 0.001). CONCLUSION: The long-term prognosis of BKVAN with acute rejection was very poor because of graft failure caused by inadequate treatment for acute rejection considering BKVAN. Therefore, we should carefully monitor the allograft status of KTRs through regular surveillance tests after treatment for BKVAN with acute rejection. Korean Society of Nephrology 2018-06 2018-06-30 /pmc/articles/PMC6027809/ /pubmed/29971212 http://dx.doi.org/10.23876/j.krcp.2018.37.2.167 Text en Copyright © 2018 by The Korean Society of Nephrology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Woo Yeong Kang, Seong Sik Jin, Kyubok Park, Sung Bae Choe, Misun Han, Seungyeup Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title | Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title_full | Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title_fullStr | Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title_full_unstemmed | Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title_short | Long-term prognosis of BK virus-associated nephropathy in kidney transplant recipients |
title_sort | long-term prognosis of bk virus-associated nephropathy in kidney transplant recipients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027809/ https://www.ncbi.nlm.nih.gov/pubmed/29971212 http://dx.doi.org/10.23876/j.krcp.2018.37.2.167 |
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