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Reproducibility of native T(1) mapping for renal tissue characterization at 3T

BACKGROUND: Advanced renal disease is characterized by adverse changes in renal structure; however, noninvasive techniques to diagnose and monitor these changes are currently lacking. PURPOSE: To evaluate the reproducibility of native T(1) mapping for renal tissue characterization. STUDY TYPE: Repro...

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Autores principales: Dekkers, Ilona A., Paiman, Elisabeth H.M., de Vries, Aiko P.J., Lamb, Hildo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585932/
https://www.ncbi.nlm.nih.gov/pubmed/30171825
http://dx.doi.org/10.1002/jmri.26207
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author Dekkers, Ilona A.
Paiman, Elisabeth H.M.
de Vries, Aiko P.J.
Lamb, Hildo J.
author_facet Dekkers, Ilona A.
Paiman, Elisabeth H.M.
de Vries, Aiko P.J.
Lamb, Hildo J.
author_sort Dekkers, Ilona A.
collection PubMed
description BACKGROUND: Advanced renal disease is characterized by adverse changes in renal structure; however, noninvasive techniques to diagnose and monitor these changes are currently lacking. PURPOSE: To evaluate the reproducibility of native T(1) mapping for renal tissue characterization. STUDY TYPE: Reproducibility study. POPULATION: Fifteen healthy volunteers (mean age 31 years, range 19–63 years), and 11 patients with diabetic nephropathy (mean age 57 years, range 51–69 years). FIELD STRENGTH/SEQUENCE: 3T, modified Look–Locker imaging (MOLLI) 5(3)3. ASSESSMENT: Intra‐ and interexamination reproducibility of voxel‐based T(1) relaxation times of renal cortex and medulla was assessed in healthy human volunteers and diabetic nephropathy patients. STATISTICAL TESTS: Reproducibility was evaluated using Bland–Altman and intraclass correlation coefficients (ICCs). RESULTS: Intra‐ and interexamination reproducibility of renal native T(1) mapping showed good–strong ICCs (0.83–0.89) for renal cortex and medulla, and moderate–good ICCs (0.62–0.81) for cortex–medulla ratio in both healthy volunteers and diabetic nephropathy patients. Intra‐ and interexamination limits of agreement were respectively (–124 msec, + 82 msec) and (–134 msec, + 98 msec) for renal cortex and (–138 msec, + 107 msec) and (–118 msec, + 151 msec) for medulla. Overall T(1) values for renal cortex (P = 0.277) and medulla (P = 0.973) were not significantly different between healthy volunteers and diabetic nephropathy patients, in contrast to the cortex–medulla ratio (P = 0.003). DATA CONCLUSION: Renal native T(1) mapping is a technique with good–strong intra‐ and examination reproducibility in both healthy volunteers and diabetic nephropathy patients. Level of Evidence: 3 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2019;49:588–596.
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spelling pubmed-65859322019-06-27 Reproducibility of native T(1) mapping for renal tissue characterization at 3T Dekkers, Ilona A. Paiman, Elisabeth H.M. de Vries, Aiko P.J. Lamb, Hildo J. J Magn Reson Imaging Original Research BACKGROUND: Advanced renal disease is characterized by adverse changes in renal structure; however, noninvasive techniques to diagnose and monitor these changes are currently lacking. PURPOSE: To evaluate the reproducibility of native T(1) mapping for renal tissue characterization. STUDY TYPE: Reproducibility study. POPULATION: Fifteen healthy volunteers (mean age 31 years, range 19–63 years), and 11 patients with diabetic nephropathy (mean age 57 years, range 51–69 years). FIELD STRENGTH/SEQUENCE: 3T, modified Look–Locker imaging (MOLLI) 5(3)3. ASSESSMENT: Intra‐ and interexamination reproducibility of voxel‐based T(1) relaxation times of renal cortex and medulla was assessed in healthy human volunteers and diabetic nephropathy patients. STATISTICAL TESTS: Reproducibility was evaluated using Bland–Altman and intraclass correlation coefficients (ICCs). RESULTS: Intra‐ and interexamination reproducibility of renal native T(1) mapping showed good–strong ICCs (0.83–0.89) for renal cortex and medulla, and moderate–good ICCs (0.62–0.81) for cortex–medulla ratio in both healthy volunteers and diabetic nephropathy patients. Intra‐ and interexamination limits of agreement were respectively (–124 msec, + 82 msec) and (–134 msec, + 98 msec) for renal cortex and (–138 msec, + 107 msec) and (–118 msec, + 151 msec) for medulla. Overall T(1) values for renal cortex (P = 0.277) and medulla (P = 0.973) were not significantly different between healthy volunteers and diabetic nephropathy patients, in contrast to the cortex–medulla ratio (P = 0.003). DATA CONCLUSION: Renal native T(1) mapping is a technique with good–strong intra‐ and examination reproducibility in both healthy volunteers and diabetic nephropathy patients. Level of Evidence: 3 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2019;49:588–596. John Wiley & Sons, Inc. 2018-09-01 2019-02 /pmc/articles/PMC6585932/ /pubmed/30171825 http://dx.doi.org/10.1002/jmri.26207 Text en © 2018 The Authors Journal of Magnetic Resonance Imaging published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Dekkers, Ilona A.
Paiman, Elisabeth H.M.
de Vries, Aiko P.J.
Lamb, Hildo J.
Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title_full Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title_fullStr Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title_full_unstemmed Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title_short Reproducibility of native T(1) mapping for renal tissue characterization at 3T
title_sort reproducibility of native t(1) mapping for renal tissue characterization at 3t
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585932/
https://www.ncbi.nlm.nih.gov/pubmed/30171825
http://dx.doi.org/10.1002/jmri.26207
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