Motion corrected 3D whole-heart SAVA T 1 mapping at 0.55 T.
| dc.catalogador | vzp | |
| dc.contributor.author | De la Sotta, Rafael I. | |
| dc.contributor.author | Crabb, Michael G. | |
| dc.contributor.author | Kunze, Karl P. | |
| dc.contributor.author | Botnar, René M. | |
| dc.contributor.author | Prieto, Claudia | |
| dc.date.accessioned | 2025-09-05T19:03:48Z | |
| dc.date.available | 2025-09-05T19:03:48Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | PURPOSE: To propose a novel highly efficient isotropic-resolution 3D whole-heart saturation-recovery and variable-flip-angle (SAVA) T 1 mapping sequence at 0.55 T, incorporating image navigator (iNAV)-based non-rigid motion correction and dictionary matching. METHODS: The proposed iNAV-based isotropic-resolution 3D whole-heart SAVA T 1 mapping sequence at 0.55 T acquires three gradient echo T 1-weighted volumes sequentially: an equilibrium contrast with 4° flip angle, and two saturation recovery T 1-weighted contrasts with 10° flip angles and different saturation delays. Sequence parameters were optimized for the lower field strength by simulations and phantom experiments. Two-dimensional iNAVs are acquired at each heartbeat to enable respiratory motion estimation and correction and 100% respiratory scan efficiency. The T 1 mapping is computed by dictionary matching, using subject-specific dictionaries based on Bloch equations simulations. Non-rigid motion correction is implemented based on respiratory bins reconstructed by iterative-SENSE and subsequent patch-based low-rank denoising, for each contrast separately. The proposed approach was evaluated in a standardized T 1 phantom and 10 healthy subjects, in comparison to spin-echo reference and 2D MOLLI, respectively. RESULTS: Excellent agreement is observed between iNAV-based SAVA T 1 mapping at 0.55 T and spin echo reference in phantom, with a R 2 = 0.998 $$ {R}^2=0.998 $$ for all phantom vials. Good image quality was obtained in vivo for the contrast images and corresponding T 1 maps in a scan time of 6:30 min ±40 s. Average and SD of myocardial T 1 values across subjects and segments was 706 ± 41 ms, which is comparable to acquired 2D MOLLI values of 681 ± 26 ms, and previously reported 2D MOLLI values of 701 ± 24 ms. Coefficient of variation values (12%) are higher than those previously reported for diaphragmatic navigator-based non-isotropic SAVA T 1 mapping at 3 T (7.4%). CONCLUSION: The proposed iNAV-based SAVA approach achieves free-breathing motion-corrected 3D whole-heart T 1 mapping at 0.55 T in approximately 7 min scan time for an isotropic resolution of 2 mm. In vivo experiments showed that the proposed sequence achieves good map quality, with comparable T 1 values and spatial variability compared to 2D MOLLI T 1 mapping. Further evaluation is warranted in patients with cardiovascular disease. | |
| dc.format.extent | 15 páginas | |
| dc.fuente.origen | ORCID | |
| dc.identifier.doi | 10.1002/mrm.70038 | |
| dc.identifier.issn | 0740-3194 | |
| dc.identifier.uri | https://doi.org/10.1002/mrm.70038 | |
| dc.identifier.uri | https://kclpure.kcl.ac.uk/portal/en/publications/03a4f106-2b37-4a43-8259-79dda825bff7 | |
| dc.identifier.uri | https://repositorio.uc.cl/handle/11534/105573 | |
| dc.information.autoruc | Escuela de Ingeniería; Botnar, Rene Michael; 0000-0003-2811-2509; 1015313 | |
| dc.information.autoruc | Escuela de Ingeniería; Prieto Vásquez, Claudia Del Carmen; 0000-0003-4602-2523; 14195 | |
| dc.language.iso | en | |
| dc.nota.acceso | contenido parcial | |
| dc.revista | Magnetic Resonance in Medicine | |
| dc.rights | acceso restringido | |
| dc.subject | Cardiac MRI | |
| dc.subject | Free-breathing | |
| dc.subject | Low-field, myocardial T1 | |
| dc.subject | Mapping | |
| dc.subject.ddc | 620 | |
| dc.subject.dewey | Ingeniería | es_ES |
| dc.title | Motion corrected 3D whole-heart SAVA T 1 mapping at 0.55 T. | |
| dc.type | artículo | |
| sipa.codpersvinculados | 1015313 | |
| sipa.codpersvinculados | 14195 | |
| sipa.trazabilidad | ORCID;2025-09-01 |
