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Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting
PURPOSE: Develop a novel 2D cardiac MR fingerprinting (MRF) approach to enable simultaneous T1, T2, T2*, and fat fraction (FF) myocardial tissue characterization in a single breath‐hold scan. METHODS: Simultaneous, co‐registered, multi‐parametric mapping of T1, T2, and FF has been recently achieved...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306903/ https://www.ncbi.nlm.nih.gov/pubmed/35081260 http://dx.doi.org/10.1002/mrm.29171 |
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author | Lima da Cruz, Gastao José Velasco, Carlos Lavin, Begoña Jaubert, Olivier Botnar, Rene Michael Prieto, Claudia |
author_facet | Lima da Cruz, Gastao José Velasco, Carlos Lavin, Begoña Jaubert, Olivier Botnar, Rene Michael Prieto, Claudia |
author_sort | Lima da Cruz, Gastao José |
collection | PubMed |
description | PURPOSE: Develop a novel 2D cardiac MR fingerprinting (MRF) approach to enable simultaneous T1, T2, T2*, and fat fraction (FF) myocardial tissue characterization in a single breath‐hold scan. METHODS: Simultaneous, co‐registered, multi‐parametric mapping of T1, T2, and FF has been recently achieved with cardiac MRF. Here, we further incorporate T2* quantification within this approach, enabling simultaneous T1, T2, T2*, and FF myocardial tissue characterization in a single breath‐hold scan. T2* quantification is achieved with an eight‐echo readout that requires a long cardiac acquisition window. A novel low‐rank motion‐corrected (LRMC) reconstruction is exploited to correct for cardiac motion within the long acquisition window. The proposed T1/T2/T2*/FF cardiac MRF was evaluated in phantom and in 10 healthy subjects in comparison to conventional mapping techniques. RESULTS: The proposed approach achieved high quality parametric mapping of T1, T2, T2*, and FF with corresponding normalized RMS error (RMSE) T1 = 5.9%, T2 = 9.6% (T2 values <100 ms), T2* = 3.3% (T2* values <100 ms), and FF = 0.8% observed in phantom scans. In vivo, the proposed approach produced higher left‐ventricular myocardial T1 values than MOLLI (1148 vs 1056 ms), lower T2 values than T2‐GraSE (42.8 vs 50.6 ms), lower T2* values than eight‐echo gradient echo (GRE) (35.0 vs 39.4 ms), and higher FF values than six‐echo GRE (0.8 vs 0.3 %) reference techniques. The proposed approach achieved considerable reduction in motion artifacts compared to cardiac MRF without motion correction, improved spatial uniformity, and statistically higher apparent precision relative to conventional mapping for all parameters. CONCLUSION: The proposed cardiac MRF approach enables simultaneous, co‐registered mapping of T1, T2, T2*, and FF in a single breath‐hold for comprehensive myocardial tissue characterization, achieving higher apparent precision than conventional methods. |
format | Online Article Text |
id | pubmed-9306903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93069032022-07-28 Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting Lima da Cruz, Gastao José Velasco, Carlos Lavin, Begoña Jaubert, Olivier Botnar, Rene Michael Prieto, Claudia Magn Reson Med Research Articles—Imaging Methodology PURPOSE: Develop a novel 2D cardiac MR fingerprinting (MRF) approach to enable simultaneous T1, T2, T2*, and fat fraction (FF) myocardial tissue characterization in a single breath‐hold scan. METHODS: Simultaneous, co‐registered, multi‐parametric mapping of T1, T2, and FF has been recently achieved with cardiac MRF. Here, we further incorporate T2* quantification within this approach, enabling simultaneous T1, T2, T2*, and FF myocardial tissue characterization in a single breath‐hold scan. T2* quantification is achieved with an eight‐echo readout that requires a long cardiac acquisition window. A novel low‐rank motion‐corrected (LRMC) reconstruction is exploited to correct for cardiac motion within the long acquisition window. The proposed T1/T2/T2*/FF cardiac MRF was evaluated in phantom and in 10 healthy subjects in comparison to conventional mapping techniques. RESULTS: The proposed approach achieved high quality parametric mapping of T1, T2, T2*, and FF with corresponding normalized RMS error (RMSE) T1 = 5.9%, T2 = 9.6% (T2 values <100 ms), T2* = 3.3% (T2* values <100 ms), and FF = 0.8% observed in phantom scans. In vivo, the proposed approach produced higher left‐ventricular myocardial T1 values than MOLLI (1148 vs 1056 ms), lower T2 values than T2‐GraSE (42.8 vs 50.6 ms), lower T2* values than eight‐echo gradient echo (GRE) (35.0 vs 39.4 ms), and higher FF values than six‐echo GRE (0.8 vs 0.3 %) reference techniques. The proposed approach achieved considerable reduction in motion artifacts compared to cardiac MRF without motion correction, improved spatial uniformity, and statistically higher apparent precision relative to conventional mapping for all parameters. CONCLUSION: The proposed cardiac MRF approach enables simultaneous, co‐registered mapping of T1, T2, T2*, and FF in a single breath‐hold for comprehensive myocardial tissue characterization, achieving higher apparent precision than conventional methods. John Wiley and Sons Inc. 2022-01-26 2022-06 /pmc/articles/PMC9306903/ /pubmed/35081260 http://dx.doi.org/10.1002/mrm.29171 Text en © 2022 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles—Imaging Methodology Lima da Cruz, Gastao José Velasco, Carlos Lavin, Begoña Jaubert, Olivier Botnar, Rene Michael Prieto, Claudia Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title | Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title_full | Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title_fullStr | Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title_full_unstemmed | Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title_short | Myocardial T1, T2, T2*, and fat fraction quantification via low‐rank motion‐corrected cardiac MR fingerprinting |
title_sort | myocardial t1, t2, t2*, and fat fraction quantification via low‐rank motion‐corrected cardiac mr fingerprinting |
topic | Research Articles—Imaging Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306903/ https://www.ncbi.nlm.nih.gov/pubmed/35081260 http://dx.doi.org/10.1002/mrm.29171 |
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