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dc.contributor.authorMorales, Manuel A
dc.contributor.authorvan den Boomen, Maaike
dc.contributor.authorNguyen, Christopher
dc.contributor.authorKalpathy-Cramer, Jayashree
dc.contributor.authorRosen, Bruce R
dc.contributor.authorStultz, Collin M
dc.contributor.authorIzquierdo-Garcia, David
dc.contributor.authorCatana, Ciprian
dc.date.accessioned2022-07-20T17:04:00Z
dc.date.available2022-07-20T17:04:00Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/143900
dc.description.abstract<jats:p>Myocardial strain analysis from cinematic magnetic resonance imaging (cine-MRI) data provides a more thorough characterization of cardiac mechanics than volumetric parameters such as left-ventricular ejection fraction, but sources of variation including segmentation and motion estimation have limited its wider clinical use. We designed and validated a fast, fully-automatic deep learning (DL) workflow to generate both volumetric parameters and strain measures from cine-MRI data consisting of segmentation and motion estimation convolutional neural networks. The final motion network design, loss function, and associated hyperparameters are the result of a thorough <jats:italic>ad hoc</jats:italic> implementation that we carefully planned specific for strain quantification, tested, and compared to other potential alternatives. The optimal configuration was trained using healthy and cardiovascular disease (CVD) subjects (<jats:italic>n</jats:italic> = 150). DL-based volumetric parameters were correlated (&amp;gt;0.98) and without significant bias relative to parameters derived from manual segmentations in 50 healthy and CVD test subjects. Compared to landmarks manually-tracked on tagging-MRI images from 15 healthy subjects, landmark deformation using DL-based motion estimates from paired cine-MRI data resulted in an end-point-error of 2.9 ± 1.5 mm. Measures of end-systolic global strain from these cine-MRI data showed no significant biases relative to a tagging-MRI reference method. On 10 healthy subjects, intraclass correlation coefficient for intra-scanner repeatability was good to excellent (&amp;gt;0.75) for all global measures and most polar map segments. In conclusion, we developed and evaluated the first end-to-end learning-based workflow for automated strain analysis from cine-MRI data to quantitatively characterize cardiac mechanics of healthy and CVD subjects.</jats:p>en_US
dc.language.isoen
dc.publisherFrontiers Media SAen_US
dc.relation.isversionof10.3389/FCVM.2021.730316en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceFrontiersen_US
dc.titleDeepStrain: A Deep Learning Workflow for the Automated Characterization of Cardiac Mechanicsen_US
dc.typeArticleen_US
dc.identifier.citationMorales, Manuel A, van den Boomen, Maaike, Nguyen, Christopher, Kalpathy-Cramer, Jayashree, Rosen, Bruce R et al. 2021. "DeepStrain: A Deep Learning Workflow for the Automated Characterization of Cardiac Mechanics." Frontiers in Cardiovascular Medicine, 8.
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.relation.journalFrontiers in Cardiovascular Medicineen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-07-20T17:00:10Z
dspace.orderedauthorsMorales, MA; van den Boomen, M; Nguyen, C; Kalpathy-Cramer, J; Rosen, BR; Stultz, CM; Izquierdo-Garcia, D; Catana, Cen_US
dspace.date.submission2022-07-20T17:00:12Z
mit.journal.volume8en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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