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Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients

BACKGROUND: Urine exosomal bkv-miR-B1-5p is associated with BK virus (BKV) nephropathy (BKVN); however, its posttransplantation changes and predictability for BKVN have not been determined in kidney transplant recipients (KTRs). METHODS: Urine exosomal bkv-miR-B1-5p and urine and plasma BKV DNA were...

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Autores principales: Jung, Su Woong, Cho, Won-Hee, Seo, Jung-Woo, Kim, Yang-Gyun, Moon, Ju-Young, Kim, Jin Sug, Kim, Chan-Duck, Chung, Byung Ha, Park, Jae Berm, Kim, Yeong Hoon, Lee, Sang-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175067/
https://www.ncbi.nlm.nih.gov/pubmed/36374933
http://dx.doi.org/10.1093/infdis/jiac440
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author Jung, Su Woong
Cho, Won-Hee
Seo, Jung-Woo
Kim, Yang-Gyun
Moon, Ju-Young
Kim, Jin Sug
Kim, Chan-Duck
Chung, Byung Ha
Park, Jae Berm
Kim, Yeong Hoon
Lee, Sang-Ho
author_facet Jung, Su Woong
Cho, Won-Hee
Seo, Jung-Woo
Kim, Yang-Gyun
Moon, Ju-Young
Kim, Jin Sug
Kim, Chan-Duck
Chung, Byung Ha
Park, Jae Berm
Kim, Yeong Hoon
Lee, Sang-Ho
author_sort Jung, Su Woong
collection PubMed
description BACKGROUND: Urine exosomal bkv-miR-B1-5p is associated with BK virus (BKV) nephropathy (BKVN); however, its posttransplantation changes and predictability for BKVN have not been determined in kidney transplant recipients (KTRs). METHODS: Urine exosomal bkv-miR-B1-5p and urine and plasma BKV DNA were measured at 2 weeks and 3, 6, and 12 months posttransplant in 83 KTRs stratified into biopsy-proven or presumptive BKVN, BKV viruria, and no evidence of BKV reactivation. Joint model, multivariable Cox model and receiver operating characteristic curve (ROC) were used to investigate the association of each assay with the following events: a composite of biopsy-proven or presumptive BKVN, and biopsy-proven BKVN. RESULTS: Urine exosomal bkv-miR-B1-5p and urine and plasma BKV DNA showed similar posttransplant time-course changes. Joint models incorporating serial values demonstrated significant associations of all assays with the events, and Cox analyses using single time point values at 2 weeks posttransplant showed that only urine exosomal bkv-miR-B1-5p was significantly associated with the events, although it did not outperform urine BKV DNA in ROC analyses. CONCLUSIONS: Urine exosomal bkv-miR-B1-5p was associated with BKVN as were urine and plasma BKV DNA loads on serial follow-up, and might have potential as a predictive marker for BKVN during the early posttransplant period. CLINICAL TRIALS REGISTRATION: Clinical Research Information Service (https://cris.nih.go.kr/cris/), KCT0001010.
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spelling pubmed-101750672023-05-13 Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients Jung, Su Woong Cho, Won-Hee Seo, Jung-Woo Kim, Yang-Gyun Moon, Ju-Young Kim, Jin Sug Kim, Chan-Duck Chung, Byung Ha Park, Jae Berm Kim, Yeong Hoon Lee, Sang-Ho J Infect Dis Major Article BACKGROUND: Urine exosomal bkv-miR-B1-5p is associated with BK virus (BKV) nephropathy (BKVN); however, its posttransplantation changes and predictability for BKVN have not been determined in kidney transplant recipients (KTRs). METHODS: Urine exosomal bkv-miR-B1-5p and urine and plasma BKV DNA were measured at 2 weeks and 3, 6, and 12 months posttransplant in 83 KTRs stratified into biopsy-proven or presumptive BKVN, BKV viruria, and no evidence of BKV reactivation. Joint model, multivariable Cox model and receiver operating characteristic curve (ROC) were used to investigate the association of each assay with the following events: a composite of biopsy-proven or presumptive BKVN, and biopsy-proven BKVN. RESULTS: Urine exosomal bkv-miR-B1-5p and urine and plasma BKV DNA showed similar posttransplant time-course changes. Joint models incorporating serial values demonstrated significant associations of all assays with the events, and Cox analyses using single time point values at 2 weeks posttransplant showed that only urine exosomal bkv-miR-B1-5p was significantly associated with the events, although it did not outperform urine BKV DNA in ROC analyses. CONCLUSIONS: Urine exosomal bkv-miR-B1-5p was associated with BKVN as were urine and plasma BKV DNA loads on serial follow-up, and might have potential as a predictive marker for BKVN during the early posttransplant period. CLINICAL TRIALS REGISTRATION: Clinical Research Information Service (https://cris.nih.go.kr/cris/), KCT0001010. Oxford University Press 2022-11-14 /pmc/articles/PMC10175067/ /pubmed/36374933 http://dx.doi.org/10.1093/infdis/jiac440 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Jung, Su Woong
Cho, Won-Hee
Seo, Jung-Woo
Kim, Yang-Gyun
Moon, Ju-Young
Kim, Jin Sug
Kim, Chan-Duck
Chung, Byung Ha
Park, Jae Berm
Kim, Yeong Hoon
Lee, Sang-Ho
Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title_full Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title_fullStr Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title_full_unstemmed Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title_short Urine Exosomal bkv-miR-B1-5p and BK Virus Nephropathy in Kidney Transplant Recipients
title_sort urine exosomal bkv-mir-b1-5p and bk virus nephropathy in kidney transplant recipients
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175067/
https://www.ncbi.nlm.nih.gov/pubmed/36374933
http://dx.doi.org/10.1093/infdis/jiac440
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