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Long-term CMV monitoring and chronic rejection in renal transplant recipients

INTRODUCTION: Cytomegalovirus (CMV) is well established to be an independent risk factor for graft loss after kidney transplantation (KTx). Monitoring for CMV in the chronic phase is not defined in the current guideline. The effects of CMV infection, including asymptomatic CMV viremia, in the chroni...

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Autores principales: Ishikawa, Shoko, Tasaki, Masayuki, Saito, Kazuhide, Nakagawa, Yuki, Ikeda, Masahiro, Takahashi, Kota, Tomita, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294236/
https://www.ncbi.nlm.nih.gov/pubmed/37384223
http://dx.doi.org/10.3389/fcimb.2023.1190794
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author Ishikawa, Shoko
Tasaki, Masayuki
Saito, Kazuhide
Nakagawa, Yuki
Ikeda, Masahiro
Takahashi, Kota
Tomita, Yoshihiko
author_facet Ishikawa, Shoko
Tasaki, Masayuki
Saito, Kazuhide
Nakagawa, Yuki
Ikeda, Masahiro
Takahashi, Kota
Tomita, Yoshihiko
author_sort Ishikawa, Shoko
collection PubMed
description INTRODUCTION: Cytomegalovirus (CMV) is well established to be an independent risk factor for graft loss after kidney transplantation (KTx). Monitoring for CMV in the chronic phase is not defined in the current guideline. The effects of CMV infection, including asymptomatic CMV viremia, in the chronic phase are unclear. METHODS: We performed a single-center retrospective study to investigate incidence of CMV infection in the chronic phase, defined as more than 1 year after KTx. We included 205 patients who received KTx between April 2004 and December 2017. The CMV pp65 antigenemia assays to detect CMV viremia were continuously performed every 1–3 months. RESULTS: The median duration of the follow-up was 80.6 (13.1–172.1) months. Asymptomatic CMV infection and CMV disease were observed in 30.7% and 2.9% in the chronic phase, respectively. We found that 10–20% of patients had CMV infections in each year after KTx which did not change over 10 years. The history of CMV infection in the early phase (within 1 year after KTx) and chronic rejection were significantly associated with CMV viremia in the chronic phase. CMV viremia in the chronic phase was significantly associated with graft loss. DISCUSSION: This is the first study to examine the incidence of CMV viremia for 10 years post KTx. Preventing latent CMV infection may decrease chronic rejection and graft loss after KTx.
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spelling pubmed-102942362023-06-28 Long-term CMV monitoring and chronic rejection in renal transplant recipients Ishikawa, Shoko Tasaki, Masayuki Saito, Kazuhide Nakagawa, Yuki Ikeda, Masahiro Takahashi, Kota Tomita, Yoshihiko Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: Cytomegalovirus (CMV) is well established to be an independent risk factor for graft loss after kidney transplantation (KTx). Monitoring for CMV in the chronic phase is not defined in the current guideline. The effects of CMV infection, including asymptomatic CMV viremia, in the chronic phase are unclear. METHODS: We performed a single-center retrospective study to investigate incidence of CMV infection in the chronic phase, defined as more than 1 year after KTx. We included 205 patients who received KTx between April 2004 and December 2017. The CMV pp65 antigenemia assays to detect CMV viremia were continuously performed every 1–3 months. RESULTS: The median duration of the follow-up was 80.6 (13.1–172.1) months. Asymptomatic CMV infection and CMV disease were observed in 30.7% and 2.9% in the chronic phase, respectively. We found that 10–20% of patients had CMV infections in each year after KTx which did not change over 10 years. The history of CMV infection in the early phase (within 1 year after KTx) and chronic rejection were significantly associated with CMV viremia in the chronic phase. CMV viremia in the chronic phase was significantly associated with graft loss. DISCUSSION: This is the first study to examine the incidence of CMV viremia for 10 years post KTx. Preventing latent CMV infection may decrease chronic rejection and graft loss after KTx. Frontiers Media S.A. 2023-06-13 /pmc/articles/PMC10294236/ /pubmed/37384223 http://dx.doi.org/10.3389/fcimb.2023.1190794 Text en Copyright © 2023 Ishikawa, Tasaki, Saito, Nakagawa, Ikeda, Takahashi and Tomita https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Ishikawa, Shoko
Tasaki, Masayuki
Saito, Kazuhide
Nakagawa, Yuki
Ikeda, Masahiro
Takahashi, Kota
Tomita, Yoshihiko
Long-term CMV monitoring and chronic rejection in renal transplant recipients
title Long-term CMV monitoring and chronic rejection in renal transplant recipients
title_full Long-term CMV monitoring and chronic rejection in renal transplant recipients
title_fullStr Long-term CMV monitoring and chronic rejection in renal transplant recipients
title_full_unstemmed Long-term CMV monitoring and chronic rejection in renal transplant recipients
title_short Long-term CMV monitoring and chronic rejection in renal transplant recipients
title_sort long-term cmv monitoring and chronic rejection in renal transplant recipients
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294236/
https://www.ncbi.nlm.nih.gov/pubmed/37384223
http://dx.doi.org/10.3389/fcimb.2023.1190794
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