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Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection
Donor‐derived cell free DNA (dd‐cfDNA) has rapidly become part of rejection surveillance following orthotopic heart transplantation. However, some patients show elevated dd‐cfDNA without clinical evidence of rejection. With the aim to provide a clinical description of this subpopulation, we retrospe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286598/ https://www.ncbi.nlm.nih.gov/pubmed/34863042 http://dx.doi.org/10.1111/ctr.14549 |
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author | Afzal, Aasim Alam, Amit van Zyl, Johanna S. Zafar, Hira Felius, Joost Hall, Shelley A. Carey, Sandra A. |
author_facet | Afzal, Aasim Alam, Amit van Zyl, Johanna S. Zafar, Hira Felius, Joost Hall, Shelley A. Carey, Sandra A. |
author_sort | Afzal, Aasim |
collection | PubMed |
description | Donor‐derived cell free DNA (dd‐cfDNA) has rapidly become part of rejection surveillance following orthotopic heart transplantation. However, some patients show elevated dd‐cfDNA without clinical evidence of rejection. With the aim to provide a clinical description of this subpopulation, we retrospectively analyzed 35 cardiac transplant recipients at our center who experienced elevated (≥.20%) dd‐cfDNA in the absence of clinical rejection, out of a total 106 recipients who had dd‐cfDNA results available during the first year. The median time to first elevated dd‐cfDNA level was 46 days, and the highest dd‐cfDNA recorded within 1 year was .31% [inter‐quartile range, .23–.45]. Twenty‐two (63%) patients experienced infections (cytomegalovirus (CMV) or other), and 16 (46%) presented with de novo donor‐specific antibodies. Cluster analysis revealed four distinct groups characterized by (a) subclinical rejection with 50% CMV (n = 16), (b) non‐CMV infections and the longest time to first elevated dd‐cfDNA (187 days) (n = 8), (c) right ventricular dysfunction (n = 6), and (d) women who showed the youngest median age (45 years) and highest median dd‐cfDNA (.50%) (n = 5). Continued prospective analysis is needed to determine if these observations warrant changes in patient management to optimize the utilization of this vital non‐invasive graft surveillance tool. |
format | Online Article Text |
id | pubmed-9286598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92865982022-07-19 Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection Afzal, Aasim Alam, Amit van Zyl, Johanna S. Zafar, Hira Felius, Joost Hall, Shelley A. Carey, Sandra A. Clin Transplant Original Articles Donor‐derived cell free DNA (dd‐cfDNA) has rapidly become part of rejection surveillance following orthotopic heart transplantation. However, some patients show elevated dd‐cfDNA without clinical evidence of rejection. With the aim to provide a clinical description of this subpopulation, we retrospectively analyzed 35 cardiac transplant recipients at our center who experienced elevated (≥.20%) dd‐cfDNA in the absence of clinical rejection, out of a total 106 recipients who had dd‐cfDNA results available during the first year. The median time to first elevated dd‐cfDNA level was 46 days, and the highest dd‐cfDNA recorded within 1 year was .31% [inter‐quartile range, .23–.45]. Twenty‐two (63%) patients experienced infections (cytomegalovirus (CMV) or other), and 16 (46%) presented with de novo donor‐specific antibodies. Cluster analysis revealed four distinct groups characterized by (a) subclinical rejection with 50% CMV (n = 16), (b) non‐CMV infections and the longest time to first elevated dd‐cfDNA (187 days) (n = 8), (c) right ventricular dysfunction (n = 6), and (d) women who showed the youngest median age (45 years) and highest median dd‐cfDNA (.50%) (n = 5). Continued prospective analysis is needed to determine if these observations warrant changes in patient management to optimize the utilization of this vital non‐invasive graft surveillance tool. John Wiley and Sons Inc. 2021-12-17 2022-03 /pmc/articles/PMC9286598/ /pubmed/34863042 http://dx.doi.org/10.1111/ctr.14549 Text en © 2021 The Authors. Clinical Transplantation published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Afzal, Aasim Alam, Amit van Zyl, Johanna S. Zafar, Hira Felius, Joost Hall, Shelley A. Carey, Sandra A. Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title | Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title_full | Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title_fullStr | Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title_full_unstemmed | Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title_short | Observed elevated donor‐derived cell free DNA in orthotopic heart transplant recipients without clinical evidence of rejection |
title_sort | observed elevated donor‐derived cell free dna in orthotopic heart transplant recipients without clinical evidence of rejection |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286598/ https://www.ncbi.nlm.nih.gov/pubmed/34863042 http://dx.doi.org/10.1111/ctr.14549 |
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