Cargando…

Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers

Cardiac Magnetic Resonance Fingerprinting (cMRF) has been demonstrated to enable robust and accurate T(1) and T(2) mapping for the detection of myocardial fibrosis and edema. However, the relatively long acquisition window (250 ms) used in previous cMRF studies might leave it vulnerable to motion ar...

Descripción completa

Detalles Bibliográficos
Autores principales: Rumac, Simone, Pavon, Anna Giulia, Hamilton, Jesse I., Rodrigues, David, Seiberlich, Nicole, Schwitter, Juerg, van Heeswijk, Ruud B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636181/
https://www.ncbi.nlm.nih.gov/pubmed/36333385
http://dx.doi.org/10.1038/s41598-022-23573-3
_version_ 1784824882333220864
author Rumac, Simone
Pavon, Anna Giulia
Hamilton, Jesse I.
Rodrigues, David
Seiberlich, Nicole
Schwitter, Juerg
van Heeswijk, Ruud B.
author_facet Rumac, Simone
Pavon, Anna Giulia
Hamilton, Jesse I.
Rodrigues, David
Seiberlich, Nicole
Schwitter, Juerg
van Heeswijk, Ruud B.
author_sort Rumac, Simone
collection PubMed
description Cardiac Magnetic Resonance Fingerprinting (cMRF) has been demonstrated to enable robust and accurate T(1) and T(2) mapping for the detection of myocardial fibrosis and edema. However, the relatively long acquisition window (250 ms) used in previous cMRF studies might leave it vulnerable to motion artifacts in patients with high heart rates. The goal of this study was therefore to compare cMRF with a short acquisition window (154 ms) and low-rank reconstruction to routine cardiac T(1) and T(2) mapping at 1.5 T. Phantom studies showed that the proposed cMRF had a high T(1) and T(2) accuracy over a wider range than routine mapping techniques. In 9 healthy volunteers, the proposed cMRF showed small but significant myocardial T(1) and T(2) differences compared to routine mapping (ΔT(1) = 1.5%, P = 0.031 and ΔT(2) = − 7.1%, P < 0.001). In 61 consecutive patients referred for CMR, the native T(1) values were slightly lower (ΔT(1) = 1.6%; P = 0.02), while T(2) values did not show statistical difference (ΔT(2) = 4.3%; P = 0.11). However, the difference was higher in post-contrast myocardial T(1) values (ΔT(1) = 12.3%; P < 0.001), which was reflected in the extracellular volume (ΔECV = 2.4%; P < 0.001). Across all subjects, the proposed cMRF had a lower precision when compared to routine techniques, although its higher spatial resolution enabled the visualization of smaller details.
format Online
Article
Text
id pubmed-9636181
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-96361812022-11-06 Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers Rumac, Simone Pavon, Anna Giulia Hamilton, Jesse I. Rodrigues, David Seiberlich, Nicole Schwitter, Juerg van Heeswijk, Ruud B. Sci Rep Article Cardiac Magnetic Resonance Fingerprinting (cMRF) has been demonstrated to enable robust and accurate T(1) and T(2) mapping for the detection of myocardial fibrosis and edema. However, the relatively long acquisition window (250 ms) used in previous cMRF studies might leave it vulnerable to motion artifacts in patients with high heart rates. The goal of this study was therefore to compare cMRF with a short acquisition window (154 ms) and low-rank reconstruction to routine cardiac T(1) and T(2) mapping at 1.5 T. Phantom studies showed that the proposed cMRF had a high T(1) and T(2) accuracy over a wider range than routine mapping techniques. In 9 healthy volunteers, the proposed cMRF showed small but significant myocardial T(1) and T(2) differences compared to routine mapping (ΔT(1) = 1.5%, P = 0.031 and ΔT(2) = − 7.1%, P < 0.001). In 61 consecutive patients referred for CMR, the native T(1) values were slightly lower (ΔT(1) = 1.6%; P = 0.02), while T(2) values did not show statistical difference (ΔT(2) = 4.3%; P = 0.11). However, the difference was higher in post-contrast myocardial T(1) values (ΔT(1) = 12.3%; P < 0.001), which was reflected in the extracellular volume (ΔECV = 2.4%; P < 0.001). Across all subjects, the proposed cMRF had a lower precision when compared to routine techniques, although its higher spatial resolution enabled the visualization of smaller details. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9636181/ /pubmed/36333385 http://dx.doi.org/10.1038/s41598-022-23573-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rumac, Simone
Pavon, Anna Giulia
Hamilton, Jesse I.
Rodrigues, David
Seiberlich, Nicole
Schwitter, Juerg
van Heeswijk, Ruud B.
Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title_full Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title_fullStr Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title_full_unstemmed Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title_short Cardiac MR fingerprinting with a short acquisition window in consecutive patients referred for clinical CMR and healthy volunteers
title_sort cardiac mr fingerprinting with a short acquisition window in consecutive patients referred for clinical cmr and healthy volunteers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636181/
https://www.ncbi.nlm.nih.gov/pubmed/36333385
http://dx.doi.org/10.1038/s41598-022-23573-3
work_keys_str_mv AT rumacsimone cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT pavonannagiulia cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT hamiltonjessei cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT rodriguesdavid cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT seiberlichnicole cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT schwitterjuerg cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers
AT vanheeswijkruudb cardiacmrfingerprintingwithashortacquisitionwindowinconsecutivepatientsreferredforclinicalcmrandhealthyvolunteers