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Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts

Interstitial fibrosis (IF) is the common pathway of chronic kidney injury in various conditions. Magnetic resonance imaging (MRI) may be a promising tool for the noninvasive assessment of IF in renal allografts. METHODS. This prospective trial was primarily designed to investigate whether the result...

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Autores principales: Beck-Tölly, Andrea, Eder, Michael, Beitzke, Dietrich, Eskandary, Farsad, Agibetov, Asan, Lampichler, Katharina, Hamböck, Martina, Regele, Heinz, Kläger, Johannes, Nackenhorst, Maja, Böhmig, Georg A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581173/
https://www.ncbi.nlm.nih.gov/pubmed/33134501
http://dx.doi.org/10.1097/TXD.0000000000001009
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author Beck-Tölly, Andrea
Eder, Michael
Beitzke, Dietrich
Eskandary, Farsad
Agibetov, Asan
Lampichler, Katharina
Hamböck, Martina
Regele, Heinz
Kläger, Johannes
Nackenhorst, Maja
Böhmig, Georg A.
author_facet Beck-Tölly, Andrea
Eder, Michael
Beitzke, Dietrich
Eskandary, Farsad
Agibetov, Asan
Lampichler, Katharina
Hamböck, Martina
Regele, Heinz
Kläger, Johannes
Nackenhorst, Maja
Böhmig, Georg A.
author_sort Beck-Tölly, Andrea
collection PubMed
description Interstitial fibrosis (IF) is the common pathway of chronic kidney injury in various conditions. Magnetic resonance imaging (MRI) may be a promising tool for the noninvasive assessment of IF in renal allografts. METHODS. This prospective trial was primarily designed to investigate whether the results of T1-weighted MRI associate with the degree of IF. Thirty-two kidney transplant recipients were subjected to 1.5-Tesla MRI scans shortly before or after routine allograft biopsies. MRI parameters [T1 and T2 relaxation times; apparent diffusion coefficient (ADC)] were assessed for cortical and medullary sections. RESULTS. Advanced IF (Banff ci score >1) was associated with higher cortical T1 (but not T2) values [1451 (median; interquartile range: 1331–1506) versus 1306 (1197–1321) ms in subjects with ci scores ≤1; P = 0.011; receiver operating characteristic area under the curve for prediction of ci > 1: 0.76]. In parallel, T1 values were associated with kidney function and proteinuria. There was also a relationship between IF and corticomedullary differences on ADC maps (receiver operating characteristic area under the curve for prediction of ci ≤ 1: 0.79). CONCLUSIONS. Our results support the use of MRI for noninvasive assessment of allograft scarring. Future studies will have to clarify the role of T1 (and ADC) mapping as a surrogate endpoint reflecting the progression of chronic graft damage.
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spelling pubmed-75811732020-10-29 Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts Beck-Tölly, Andrea Eder, Michael Beitzke, Dietrich Eskandary, Farsad Agibetov, Asan Lampichler, Katharina Hamböck, Martina Regele, Heinz Kläger, Johannes Nackenhorst, Maja Böhmig, Georg A. Transplant Direct Kidney Transplantation Interstitial fibrosis (IF) is the common pathway of chronic kidney injury in various conditions. Magnetic resonance imaging (MRI) may be a promising tool for the noninvasive assessment of IF in renal allografts. METHODS. This prospective trial was primarily designed to investigate whether the results of T1-weighted MRI associate with the degree of IF. Thirty-two kidney transplant recipients were subjected to 1.5-Tesla MRI scans shortly before or after routine allograft biopsies. MRI parameters [T1 and T2 relaxation times; apparent diffusion coefficient (ADC)] were assessed for cortical and medullary sections. RESULTS. Advanced IF (Banff ci score >1) was associated with higher cortical T1 (but not T2) values [1451 (median; interquartile range: 1331–1506) versus 1306 (1197–1321) ms in subjects with ci scores ≤1; P = 0.011; receiver operating characteristic area under the curve for prediction of ci > 1: 0.76]. In parallel, T1 values were associated with kidney function and proteinuria. There was also a relationship between IF and corticomedullary differences on ADC maps (receiver operating characteristic area under the curve for prediction of ci ≤ 1: 0.79). CONCLUSIONS. Our results support the use of MRI for noninvasive assessment of allograft scarring. Future studies will have to clarify the role of T1 (and ADC) mapping as a surrogate endpoint reflecting the progression of chronic graft damage. Lippincott Williams & Wilkins 2020-07-15 /pmc/articles/PMC7581173/ /pubmed/33134501 http://dx.doi.org/10.1097/TXD.0000000000001009 Text en Copyright © 2020 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Kidney Transplantation
Beck-Tölly, Andrea
Eder, Michael
Beitzke, Dietrich
Eskandary, Farsad
Agibetov, Asan
Lampichler, Katharina
Hamböck, Martina
Regele, Heinz
Kläger, Johannes
Nackenhorst, Maja
Böhmig, Georg A.
Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title_full Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title_fullStr Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title_full_unstemmed Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title_short Magnetic Resonance Imaging for Evaluation of Interstitial Fibrosis in Kidney Allografts
title_sort magnetic resonance imaging for evaluation of interstitial fibrosis in kidney allografts
topic Kidney Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581173/
https://www.ncbi.nlm.nih.gov/pubmed/33134501
http://dx.doi.org/10.1097/TXD.0000000000001009
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