Early Assessment of Renal Transplants Using BOLD-MRI: Promising Results
Non-invasive evaluation of renal transplant function is essential to minimize and manage acute renal rejection (AR). A computer-assisted diagnostic (CAD) system is developed to evaluate kidney function post-transplantation. The developed CAD system utilizes the amount of blood-oxygenation extracted...
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Published in | 2019 IEEE International Conference on Image Processing (ICIP) Vol. 2019; pp. 1395 - 1399 |
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Main Authors | , , , , , , , , , , |
Format | Conference Proceeding Journal Article |
Language | English |
Published |
IEEE
01.09.2019
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Subjects | |
Online Access | Get full text |
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Summary: | Non-invasive evaluation of renal transplant function is essential to minimize and manage acute renal rejection (AR). A computer-assisted diagnostic (CAD) system is developed to evaluate kidney function post-transplantation. The developed CAD system utilizes the amount of blood-oxygenation extracted from 3D (2D + time) blood oxygen level-dependent magnetic resonance imaging (BOLD-MRI) to estimate renal function. BOLD-MRI scans were acquired at five different echo-times (2, 7, 12, 17, and 22) ms from 15 transplant patients. The developed CAD system first segments kidneys using the level-sets method followed by estimation of the amount of deoxyhemoglobin, also known as apparent relaxation rate (R2*). These R2* estimates are used as discriminatory features (global features (mean R2*) and local features (pixel-wise R2*)) to train and test state-of-the-art machine learning classifiers to differentiate between non-rejection (NR) and AR. Using a leave-one-out cross-validation approach along with a multi-layer preceptron neural network (MLP-NN) classifier, the CAD system demonstrated 93.3% accuracy, 100% sensitivity, and 90% specificity in distinguishing AR from NR. These preliminary results demonstrate the efficacy of the CAD system to detect renal allograft status non-invasively. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1522-4880 2381-8549 |
DOI: | 10.1109/ICIP.2019.8803042 |