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Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients

Despite new advancements in surgical tools and therapies, exposure to immunosuppressive drugs related to non-immune and immune injuries can cause slow deterioration and premature failure of organ transplants. Diagnosis of these injuries by non-invasive urine monitoring would be a significant clinica...

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Autores principales: Sigdel, Tara K., Schroeder, Andrew W., Yang, Joshua Y. C., Sarwal, Reuben D., Liberto, Juliane M., Sarwal, Minnie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465632/
https://www.ncbi.nlm.nih.gov/pubmed/32707952
http://dx.doi.org/10.3390/jcm9082341
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author Sigdel, Tara K.
Schroeder, Andrew W.
Yang, Joshua Y. C.
Sarwal, Reuben D.
Liberto, Juliane M.
Sarwal, Minnie M.
author_facet Sigdel, Tara K.
Schroeder, Andrew W.
Yang, Joshua Y. C.
Sarwal, Reuben D.
Liberto, Juliane M.
Sarwal, Minnie M.
author_sort Sigdel, Tara K.
collection PubMed
description Despite new advancements in surgical tools and therapies, exposure to immunosuppressive drugs related to non-immune and immune injuries can cause slow deterioration and premature failure of organ transplants. Diagnosis of these injuries by non-invasive urine monitoring would be a significant clinical advancement for patient management, especially in pediatric cohorts. We investigated the metabolomic profiles of biopsy matched urine samples from 310 unique kidney transplant recipients using gas chromatography–mass spectrometry (GC-MS). Focused metabolite panels were identified that could detect biopsy confirmed acute rejection with 92.9% sensitivity and 96.3% specificity (11 metabolites) and could differentiate BK viral nephritis (BKVN) from acute rejection with 88.9% sensitivity and 94.8% specificity (4 metabolites). Overall, targeted metabolomic analyses of biopsy-matched urine samples enabled the generation of refined metabolite panels that non-invasively detect graft injury phenotypes with high confidence. These urine biomarkers can be rapidly assessed for non-invasive diagnosis of specific transplant injuries, opening the window for precision transplant medicine.
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spelling pubmed-74656322020-09-04 Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients Sigdel, Tara K. Schroeder, Andrew W. Yang, Joshua Y. C. Sarwal, Reuben D. Liberto, Juliane M. Sarwal, Minnie M. J Clin Med Article Despite new advancements in surgical tools and therapies, exposure to immunosuppressive drugs related to non-immune and immune injuries can cause slow deterioration and premature failure of organ transplants. Diagnosis of these injuries by non-invasive urine monitoring would be a significant clinical advancement for patient management, especially in pediatric cohorts. We investigated the metabolomic profiles of biopsy matched urine samples from 310 unique kidney transplant recipients using gas chromatography–mass spectrometry (GC-MS). Focused metabolite panels were identified that could detect biopsy confirmed acute rejection with 92.9% sensitivity and 96.3% specificity (11 metabolites) and could differentiate BK viral nephritis (BKVN) from acute rejection with 88.9% sensitivity and 94.8% specificity (4 metabolites). Overall, targeted metabolomic analyses of biopsy-matched urine samples enabled the generation of refined metabolite panels that non-invasively detect graft injury phenotypes with high confidence. These urine biomarkers can be rapidly assessed for non-invasive diagnosis of specific transplant injuries, opening the window for precision transplant medicine. MDPI 2020-07-22 /pmc/articles/PMC7465632/ /pubmed/32707952 http://dx.doi.org/10.3390/jcm9082341 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sigdel, Tara K.
Schroeder, Andrew W.
Yang, Joshua Y. C.
Sarwal, Reuben D.
Liberto, Juliane M.
Sarwal, Minnie M.
Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title_full Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title_fullStr Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title_full_unstemmed Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title_short Targeted Urine Metabolomics for Monitoring Renal Allograft Injury and Immunosuppression in Pediatric Patients
title_sort targeted urine metabolomics for monitoring renal allograft injury and immunosuppression in pediatric patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465632/
https://www.ncbi.nlm.nih.gov/pubmed/32707952
http://dx.doi.org/10.3390/jcm9082341
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