Evidence map›Paper›PMID 41453741›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance

Cardiac function assessment with deep-learning-based automatic segmentation of free-running four-dimensional whole-heart cardiovascular magnetic resonance.

Augustin C Ogier, Salomé Baup, Gorun Ilanjian, Aisha Touray, Angela Rocca, Jaume Banús, Isabel Montón Quesada, Martin Nicoletti, Jean-Baptiste Ledoux, Jonas Richiardi and 6 more

Registry-linked trialAbstract readValidation Study
In one paragraph

Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07613398 (Assessment and Validation of the Established Free-Running Framework for Cardiac Function by Magnetic Resonance Imaging), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07613398 not yet recruitingnot on this map

Assessment and Validation of the Established Free-Running Framework for Cardiac Function by Magnetic Resonance Imaging (FAST-CMR): An International Multi-Center, Multi-Vendor Study at 1.5T

Typeobservational_patient_registrySponsorMatthias StuberRan2026 to 2030Enrolled300ConditionsCongenital Heart Diseases, Cardiac Diseases
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Augustin C OgierDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland. Electronic address: augustin.ogier@gmail.com.
Salomé BaupDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Gorun IlanjianDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Aisha TourayDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Angela RoccaCardiovascular Department, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Jaume BanúsDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Isabel Montón QuesadaDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Martin NicolettiDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Jean-Baptiste LedouxDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; CIBM Center for Biomedical Imaging, Lausanne, Switzerland.
Jonas RichiardiDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; CIBM Center for Biomedical Imaging, Lausanne, Switzerland.
Robert J HoltackersDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; Department of Radiology & Nuclear Medicine, Maastricht University Medical Centre, the Netherlands.
Jérôme YerlyDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; CIBM Center for Biomedical Imaging, Lausanne, Switzerland.
Matthias StuberDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; CIBM Center for Biomedical Imaging, Lausanne, Switzerland.
Roger HullinCardiovascular Department, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
David RotzingerDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Ruud B van HeeswijkDepartment of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFree-running (FR) cardiac magnetic resonance imaging (MRI) enables free-breathing electrocardiogram (ECG)-free fully dynamic five-dimensional (5D) (three-dimensional [3D] spatial+cardiac+respiration dimensions) imaging but poses significant challenges for clinical integration due to the volume of data and complexity of image analysis. Existing segmentation methods are tailored to two-dimensional (2D) cine or static 3D acquisitions and cannot leverage the unique spatial-temporal wealth of FR data. The aim of this study was to develop and validate a deep learning (DL)-based segmentation framework for isotropic 3D+cardiac cycle FR cardiac MRI that enables accurate, fast, and clinically meaningful anatomical and functional analysis.

methodsFree-running, contrast-free balanced steady-state free precession (bSSFP) acquisitions at 1.5T and contrast-enhanced gradient-recalled echo (GRE) acquisitions at 3T were used to reconstruct motion-resolved 5D datasets. From these, the end-expiratory respiratory phase was retained to yield fully isotropic four-dimensional (4D) datasets. Automatic propagation of a limited set of manual segmentations was used to segment the left and right ventricular blood pool (LVB, RVB) and left-ventricular myocardium (LVM) on reformatted short-axis (SAX) end-systolic (ES) and end-diastolic (ED) images. These were used to train a 3D nnU-Net model. Validation was performed using geometric metrics (Dice similarity coefficient [DSC], relative volume difference [RVD]), clinical metrics (ED and ES volumes, ejection fraction [EF]), and physiological consistency metrics (systole-diastole LVM volume mismatch and LV-RV stroke volume agreement). To assess the robustness and flexibility of the approach, we evaluated multiple additional DL training configurations, such as using 4D propagation-based data augmentation to incorporate all cardiac phases into training.

resultsThe main proposed method achieved automatic segmentation within a minute, delivering high geometric accuracy and consistency (DSC: 0.94 ± 0.01 [LVB], 0.86 ± 0.02 [LVM], 0.92 ± 0.01 [RVB]; RVD: 2.7%, 5.8%, 4.5%). Clinical LV metrics showed excellent agreement (ICC >0.98 for EDV/ESV/EF, bias <2 mL for EDV/ESV, <1% for EF), while RV metrics remained clinically reliable (ICC >0.93 for EDV/ESV/EF, bias <1 mL for EDV/ESV, <1% for EF) but exhibited wider limits of agreement. Training on all cardiac phases improved temporal coherence, reducing LVM volume mismatch from 4.0% to 2.6%.

conclusionThis study validates a DL-based method for fast and accurate segmentation of whole-heart free-running 4D cardiac MRI. Robust performance across diverse protocols and evaluation with complementary metrics that match state-of-the-art benchmarks supports its integration into clinical and research workflows, helping to overcome a key barrier to the broader adoption of free-running imaging.

Indexed as

Deep LearningImage Interpretation, Computer-AssistedMagnetic Resonance Imaging, CineVentricular Function, LeftVentricular Function, RightAutomationHumansPredictive Value of TestsReproducibility of ResultsStroke Volume3D+t imagingCardiac MRICardiac segmentationDeep learningFree-runningIsotropic imaging

Identifiers

PMID41453741
PMCPMC13112478

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.