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944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients
BACKGROUND: Cytomegalovirus (CMV) infection continues to cause morbidity in kidney transplant recipients, despite prophylaxis and pre-emptive therapy. Predictors of poor outcomes remain incompletely characterized. We questioned whether markers of CMV replication (CMV peak viral load, recurrent episo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643944/ http://dx.doi.org/10.1093/ofid/ofab466.1139 |
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author | Avery, Robin K Avery, Robin K Ostrander, Darin B Lu, Na Akinwande, Felicia Kim, Min Young Gopinath, Shilpa Permpalung, Nitipong Ezennia, Obichukwu Tang, Yuexin Marr, Kieren |
author_facet | Avery, Robin K Avery, Robin K Ostrander, Darin B Lu, Na Akinwande, Felicia Kim, Min Young Gopinath, Shilpa Permpalung, Nitipong Ezennia, Obichukwu Tang, Yuexin Marr, Kieren |
author_sort | Avery, Robin K |
collection | PubMed |
description | BACKGROUND: Cytomegalovirus (CMV) infection continues to cause morbidity in kidney transplant recipients, despite prophylaxis and pre-emptive therapy. Predictors of poor outcomes remain incompletely characterized. We questioned whether markers of CMV replication (CMV peak viral load, recurrent episodes, or duration of CMV DNAemia) are associated with adverse outcomes in the current era. METHODS: We studied 605 people who underwent kidney transplant at Johns Hopkins University (2010 – 2018). Mean follow-up was 45.5 months. The average age was 51.85 years and 39.7% were female. Donor-seropositive, recipient seronegative (D+/R-) patients received valganciclovir 900 mg/day for 6 months, while R+ patients received valganciclovir 450 mg/day for 3 months. CMV recurrence was defined as CMV DNAemia after two undetectable CMV PCR’s. Outcomes of acute rejection, graft failure, and death were evaluated in univariate analysis; p values were calculated by Fisher’s exact test. RESULTS: Peak CMV viral load was not associated with any outcomes (Table 1). There was a trend of increased graft failure in people who had long duration ( >6 month) DNAemia (Table 2). More than two episodes of CMV reactivation was associated with graft failure and rejection (Table 3). [Image: see text] [Image: see text] [Image: see text] CONCLUSION: CMV reactivation is associated with kidney rejection and failure in univariate models. Multivariate analyses and longitudinal modeling will provide increased data upon which to better instruct preventative strategies. ACKNOWLEDGMENTS: Funding for the research study was provided by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA DISCLOSURES: Robin K. Avery, MD, Aicuris (Grant/Research Support)Astellas (Grant/Research Support)Chimerix (Research Grant or Support)Merck (Grant/Research Support)Oxford Immunotec (Grant/Research Support)Qiagen (Grant/Research Support)Takeda/Shire (Grant/Research Support) Yuexin Tang, PhD, JnJ (Other Financial or Material Support, Spouse’s employment)Merck & Co., Inc. (Employee, Shareholder) Kieren Marr, MD, Merck (Grant/Research Support, Advisor or Review Panel member) |
format | Online Article Text |
id | pubmed-8643944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86439442021-12-06 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients Avery, Robin K Avery, Robin K Ostrander, Darin B Lu, Na Akinwande, Felicia Kim, Min Young Gopinath, Shilpa Permpalung, Nitipong Ezennia, Obichukwu Tang, Yuexin Marr, Kieren Open Forum Infect Dis Poster Abstracts BACKGROUND: Cytomegalovirus (CMV) infection continues to cause morbidity in kidney transplant recipients, despite prophylaxis and pre-emptive therapy. Predictors of poor outcomes remain incompletely characterized. We questioned whether markers of CMV replication (CMV peak viral load, recurrent episodes, or duration of CMV DNAemia) are associated with adverse outcomes in the current era. METHODS: We studied 605 people who underwent kidney transplant at Johns Hopkins University (2010 – 2018). Mean follow-up was 45.5 months. The average age was 51.85 years and 39.7% were female. Donor-seropositive, recipient seronegative (D+/R-) patients received valganciclovir 900 mg/day for 6 months, while R+ patients received valganciclovir 450 mg/day for 3 months. CMV recurrence was defined as CMV DNAemia after two undetectable CMV PCR’s. Outcomes of acute rejection, graft failure, and death were evaluated in univariate analysis; p values were calculated by Fisher’s exact test. RESULTS: Peak CMV viral load was not associated with any outcomes (Table 1). There was a trend of increased graft failure in people who had long duration ( >6 month) DNAemia (Table 2). More than two episodes of CMV reactivation was associated with graft failure and rejection (Table 3). [Image: see text] [Image: see text] [Image: see text] CONCLUSION: CMV reactivation is associated with kidney rejection and failure in univariate models. Multivariate analyses and longitudinal modeling will provide increased data upon which to better instruct preventative strategies. ACKNOWLEDGMENTS: Funding for the research study was provided by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA DISCLOSURES: Robin K. Avery, MD, Aicuris (Grant/Research Support)Astellas (Grant/Research Support)Chimerix (Research Grant or Support)Merck (Grant/Research Support)Oxford Immunotec (Grant/Research Support)Qiagen (Grant/Research Support)Takeda/Shire (Grant/Research Support) Yuexin Tang, PhD, JnJ (Other Financial or Material Support, Spouse’s employment)Merck & Co., Inc. (Employee, Shareholder) Kieren Marr, MD, Merck (Grant/Research Support, Advisor or Review Panel member) Oxford University Press 2021-12-04 /pmc/articles/PMC8643944/ http://dx.doi.org/10.1093/ofid/ofab466.1139 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Abstracts Avery, Robin K Avery, Robin K Ostrander, Darin B Lu, Na Akinwande, Felicia Kim, Min Young Gopinath, Shilpa Permpalung, Nitipong Ezennia, Obichukwu Tang, Yuexin Marr, Kieren 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title | 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title_full | 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title_fullStr | 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title_full_unstemmed | 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title_short | 944. CMV Peak Viral Load, Recurrence, Duration, and Outcomes in Kidney Transplant Recipients |
title_sort | 944. cmv peak viral load, recurrence, duration, and outcomes in kidney transplant recipients |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643944/ http://dx.doi.org/10.1093/ofid/ofab466.1139 |
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