Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lima da Cruz, Gastao José, Velasco, Carlos, Lavin, Begoña, Jaubert, Olivier, Botnar, Rene Michael, Prieto, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784752646059458560
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
work_keys_str_mv AT limadacruzgastaojose myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting
AT velascocarlos myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting
AT lavinbegona myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting
AT jaubertolivier myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting
AT botnarrenemichael myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting
AT prietoclaudia myocardialt1t2t2andfatfractionquantificationvialowrankmotioncorrectedcardiacmrfingerprinting