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Understanding and using AlloSure donor derived cell-free DNA
Renal transplant is a lifesaving and cost-effective intervention for patients with End Stage Renal Failure. Yet it is often regarded as replacement therapy rather than a cure given the overall failure rate over time. With a shortage of organs, this global issue has been further compounded by increas...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429580/ https://www.ncbi.nlm.nih.gov/pubmed/32683591 http://dx.doi.org/10.1007/s12551-020-00713-5 |
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author | Seeto, R. K. Fleming, J. N. Dholakia, S. Dale, B. L. |
author_facet | Seeto, R. K. Fleming, J. N. Dholakia, S. Dale, B. L. |
author_sort | Seeto, R. K. |
collection | PubMed |
description | Renal transplant is a lifesaving and cost-effective intervention for patients with End Stage Renal Failure. Yet it is often regarded as replacement therapy rather than a cure given the overall failure rate over time. With a shortage of organs, this global issue has been further compounded by increased incidences of obesity, hypertension and diabetes, such that the disease burden and need for transplantation continues to increase. Considering the lifetime of immunosupression in transplant patients, there will also be significant associated co-morbidities By leveraging the advances in innovation in Next Generation Sequencing, the field of transplant can now monitor patients with an optimized surveillance schedule, and change the care paradigm in the post-transplant landscape. Notably, low grade inflammation is an independent risk for mortality across different disease states. In transplantation, sub-clinical inflammation enhances acute and chronic rejection, as well as accelerates pathologies that leads to graft loss. Cell free DNA has been shown to be increased in inflammatory processes as we all as provide an independent predictor of all-cause mortality. This review considers the utility of AlloSure, a donor derived cell free DNA molecular surveillance tool, which has shown new clinical insights on how best to manage renal transplant patients, and how to improve patient outcomes. |
format | Online Article Text |
id | pubmed-7429580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-74295802020-08-20 Understanding and using AlloSure donor derived cell-free DNA Seeto, R. K. Fleming, J. N. Dholakia, S. Dale, B. L. Biophys Rev Review Renal transplant is a lifesaving and cost-effective intervention for patients with End Stage Renal Failure. Yet it is often regarded as replacement therapy rather than a cure given the overall failure rate over time. With a shortage of organs, this global issue has been further compounded by increased incidences of obesity, hypertension and diabetes, such that the disease burden and need for transplantation continues to increase. Considering the lifetime of immunosupression in transplant patients, there will also be significant associated co-morbidities By leveraging the advances in innovation in Next Generation Sequencing, the field of transplant can now monitor patients with an optimized surveillance schedule, and change the care paradigm in the post-transplant landscape. Notably, low grade inflammation is an independent risk for mortality across different disease states. In transplantation, sub-clinical inflammation enhances acute and chronic rejection, as well as accelerates pathologies that leads to graft loss. Cell free DNA has been shown to be increased in inflammatory processes as we all as provide an independent predictor of all-cause mortality. This review considers the utility of AlloSure, a donor derived cell free DNA molecular surveillance tool, which has shown new clinical insights on how best to manage renal transplant patients, and how to improve patient outcomes. Springer Berlin Heidelberg 2020-07-18 /pmc/articles/PMC7429580/ /pubmed/32683591 http://dx.doi.org/10.1007/s12551-020-00713-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Seeto, R. K. Fleming, J. N. Dholakia, S. Dale, B. L. Understanding and using AlloSure donor derived cell-free DNA |
title | Understanding and using AlloSure donor derived cell-free DNA |
title_full | Understanding and using AlloSure donor derived cell-free DNA |
title_fullStr | Understanding and using AlloSure donor derived cell-free DNA |
title_full_unstemmed | Understanding and using AlloSure donor derived cell-free DNA |
title_short | Understanding and using AlloSure donor derived cell-free DNA |
title_sort | understanding and using allosure donor derived cell-free dna |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429580/ https://www.ncbi.nlm.nih.gov/pubmed/32683591 http://dx.doi.org/10.1007/s12551-020-00713-5 |
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