Abstract
Four-dimensional flow magnetic resonance imaging (MRI) has evolved as a non-invasive imaging technique to visualize and quantify blood flow in the heart and vessels. Hemodynamic parameters derived from 4D flow MRI, such as net flow and peak velocities, but also kinetic energy, turbulent kinetic energy, viscous energy loss, and wall shear stress have shown to be of diagnostic relevance for cardiovascular diseases. 4D flow MRI, however, has several limitations. Its long acquisition times and its limited spatio-temporal resolutions lead to inaccuracies in velocity measurements in small and low-flow vessels and near the vessel wall. Additionally, 4D flow MRI requires long post-processing times, since inaccuracies due to the measurement process need to be corrected for and parameter quantification requires 2D and 3D contour drawing. Several machine learning (ML) techniques have been proposed to overcome these limitations. Existing scan acceleration methods have been extended using ML for image reconstruction and ML based super-resolution methods have been used to assimilate high-resolution computational fluid dynamic simulations and 4D flow MRI, which leads to more realistic velocity results. ML efforts have also focused on the automation of other post-processing steps, by learning phase corrections and anti-aliasing. To automate contour drawing and 3D segmentation, networks such as the U-Net have been widely applied. This review summarizes the latest ML advances in 4D flow MRI with a focus on technical aspects and applications. It is divided into the current status of fast and accurate 4D flow MRI data generation, ML based post-processing tools for phase correction and vessel delineation and the statistical evaluation of blood flow.
Introduction
Since its emergence in 1993 (–), four-dimensional (4D) flow magnetic resonance imaging (MRI) has evolved as a non-invasive imaging technique to visualize and quantify blood flow and has been used for clinical imaging since the early 2000s (, ). 4D flow MRI is based on a time-resolved 3D phase contrast MRI sequence and is widely applied to the heart and vessels.
The quantification of net flow and peak velocities from 4D flow MRI has shown to be of diagnostic relevance for cardiovascular diseases such as the grading of stenoses, aortic coarctation, or aortic- and mitral valve regurgitation (–). Also, the visualization of the direction of the blood flow is important, for example in aortic aneurysms, aortic dissections and coarctations, in hypertrophy cardiomyopathy (, ), as well as in congenital heart disease, such as univentricular hearts or transposition of the great arteries (, ). Moreover, 4D flow MRI allows the direct quantification of regurgitant flow compared to traditional indirect methods (i.e., subtracting stroke volume calculated from aortic 2D flow MRI from stroke volume measured by left ventricular segmentation) in mitral valve insufficiency (). Furthermore, 3D visualization of the blood flow using pathlines can help interpreting complex flow patterns pre- and post-surgery, such as the Fontan procedure (). Also, other biomarkers such as kinetic energy (KE) (, ), turbulent kinetic energy (TKE) (, ), viscous energy (VE) loss (), wall shear stress (WSS) (, ) or pulse wave velocity (PWV) () have shown significant differences in patients with cardiovascular disease compared to normal subjects.
Four-dimensional flow MRI, however, has several limitations. Due to its velocity encoding scheme, 4D flow MRI takes at least four times as long as cine MRI scans (i.e., around 10 min). This poses limits on the clinical application due to additional costs, patient discomfort and motion artifacts. Additionally, limited spatio-temporal resolutions, constrained by the signal-to-noise-ratio (SNR) and scan time, lead to inaccuracies in velocity measurements in small vessels, low-flow venous vessels and near the vessel wall due to partial volume effects (). This in turn creates inaccurate grading of stenoses and inaccuracies in WSS estimation (, ). Additionally, 4D flow MRI is subject to inherent inaccuracies of the MRI measurement process such as residual phase errors, induced by eddy currents, concomitant fields, or even mechanical vibrations (), which can lead to errors in velocity estimations. Although tuning of the scanners’ pre-emphasis can help to correct for non-linearities in the gradient field, these inaccuracies, as well as phase aliasing effects, must be corrected for retrospectively, creating long post-processing times using dedicated software. The post-processing times are prolonged as net flow and peak velocities are typically evaluated by (manually) placed 2D planes and contours at the location of the corresponding vessel or valve within the 3D acquisition. Parameters such as KE, VE, TKE and WSS require even a careful delineation of the 3D vessel lumen.
Various machine learning (ML) techniques have been proposed to overcome these limitations. Existing scan acceleration methods, such as compressed sensing (CS) (–) have been extended using ML reconstructions which are able to speed up the image reconstruction time up to a couple of seconds (). Also, ML super-resolution methods can assimilate high-resolution computational fluid dynamic (CFD) simulations and 4D flow MRI, which leads to more realistic velocity results. ML based techniques, such as U-Nets, used to localize vessels and segment vessel boundaries, have been applied to 4D flow MRI to automate contour drawing and 3D segmentation. ML efforts have also focused on the automation and acceleration of other post-processing steps, by learning phase corrections and anti-aliasing.
This review summarizes the latest ML advances in 4D flow MRI with a focus on technical aspects and applications, including all original research articles published on the topics of (4D) flow MRI and ML published until November 2022. It is divided into the current status of (1) scan acceleration and image reconstruction, (2) super resolution and data assimilation for fast and accurate 4D flow MRI data generation, as well as ML based post-processing methods for (3) phase corrections, (4) vessel segmentation and (5) the statistical evaluation of blood flow.
Scan acceleration and image reconstruction
4D flow MRI uses additional magnetic field gradients to encode the velocity of moving blood. These gradients are applied to each spatial direction separately, which results in four different images, the reference image and three flow encoded images, also called 4-point encoding (Figure 1A). As the scan time is therefore four times as long, various acceleration techniques have been proposed (, –). These acceleration methods skip datapoints in k-space (undersampling), which creates aliasing artifacts in the image when using a conventional reconstruction. Most image reconstruction algorithms of these techniques take advantage of information redundancies – similar to those used for image compression – such that the full information content can be derived (). However, the runtimes for those (iterative) reconstruction algorithms range between 10 and 60 mins, a drawback that can be tackled with machine learning (ML) approaches.
FIGURE 1
Most approaches for ML image reconstruction are based on artifact-removal of undersampled data in image space, rather than training a network to retrieve the full image content directly from the undersampled k-space. In 2019, Vishnevsky et al. (
Super resolution and data assimilation
To increase the spatio-temporal resolution of 4D flow MRI, which is limited by SNR and scan time, ML super-resolution techniques can be applied. These techniques learn on paired high- and low-resolution datasets to resolve an image resolution higher than the input resolution. As there is typically a lack of high-resolution in vivo data, most super-resolution approaches for 4D flow MRI rely on synthetic images created by CFD simulations. These simulations solve the Navier Stokes equation in a given vessel geometry and under given inflow conditions and can be computed at resolutions much higher than the maximum achievable resolutions with 4D flow MRI, while maintaining correct physics.
In 2020, Ferdian et al. (
FIGURE 2

Overview of frameworks for 4D flow MRI super-resolution training and data assimilation for 4D flow MRI and CFD data: Ferdian et al. (aortic simulation) (
For ML it can be advantageous (faster, more accurate, less training data) to restrict the space of solutions. Generally, data fidelity terms in the loss function of neural networks minimize the distance between the predicted output and the measured data. Physics-informed networks include a regularization part that enforces the underlying physical principles of a given dataset. For 4D flow MRI this can for example be the conservation of mass and momentum in the flow domain, which leads to a correct solution even with limited training data (
4D flow derived biomarkers, such as WSS, have been associated with endothelial cell remodeling, for regions of low WSS (or high oscillatory WSS) in particular. Also, high WSS has been associated with disease patterns such as in aortic stenosis and aortic dissection. However, limited spatial resolution, partial volume effects and segmentation inaccuracy do not allow for accurate WSS, which is typically solved with curve-fitting and interpolation (
Phase corrections
Since velocity maps are derived from the phase of the 4D flow MRI signal, sources that introduce phase offsets, such as eddy currents, can impair the data quality. Phase corrections and anti-aliasing can be performed retrospectively to the acquisition but are user-dependent and time-consuming. ML techniques, however, can learn and apply these corrections.
Eddy current induced background phase can be corrected for by linear or polynomial fits of the phase in static tissue regions. The calculated phase error fields can then be applied the flow regions to correct the estimated velocities. You et al. (
Aliasing effects, or phase-wraps, can occur if the velocity encoding, defined by the VENC, was chosen too low. High velocities, higher than the VENC value, will appear as wrapped phases (transitioning from + π to –π) in the velocity map (Figure 3A), which must be corrected for retrospectively. The correction, however, requires the identification of the aliased voxel in 3D and for all time frames. There are several semi-automatic solutions that support 2D voxel wise un-wrapping by region-merging and graph cut optimization (
FIGURE 3

(A) Simulated parabolic flow with a central peak velocity of 220 cm/s and the aliasing effect create in the phase-difference image and the velocity map when a lower VENC e.g., of 200 cm/s is chosen. (B) Temporal evolution of the magnitude and PC-MRA signal in an aortic 4D flow MRI dataset. Magnitude images do not allow for fast segmentations based on thresholding as blood and tissue have a similar contrast. PC-MRA images lose their signal when there is no apparent blood flow e.g., during diastole.
Vessel segmentation
4D flow MRI requires accurate delineation of the vessel lumen for calculation of mean velocities, flow and WSS. The blood-tissue contrast of the sequence is low, especially without the use of contrast-agents, which is why for segmentation angiogram-like images are generated from the absolute velocity. These PC-MRAs can be calculated in a time-resolved way, but do not have sufficient signal in regions and time frames with low velocities, which is why they cannot be used for accurate, fully automated segmentations (see Figure 3B). 3D segmentation is therefore done in a semi-automatic way for static images and there is a strong need for fast, robust and automatic delineations.
Classifying machine learning tasks like the U-Net (
Bratt et al. (
In 2020, Berhane et al. (
So far, only limited studies exist on training time-resolved segmentations from 4D flow MRI. However, time-resolved segmentations are of interest when investigating stiffness by PWV (
To avoid the problem of poor myocardium-to-blood contrast in 4D flow MRI and time intensive pre-registration on atlases, Corrado et al. (
Corrado et al. (
Contrast enhanced 4D flow MRI is used for many clinical examinations and creates a better blood-tissue contrast than conventional 4D flow MRI. In medical imaging, realistic but fictitious images can be produced by generative adversarial networks (GANs), and CycleGANs (
Statistical evaluation of blood flow
ML has the potential to support the statistical classification of healthy controls and patients with cardiovascular disease based on 4D flow MRI data using supervised or unsupervised learning. For classification, typically a set of hemodynamic features is derived from the data (such as velocity, vorticity, etc.), then the number of features is reduced by a feature-selection step e.g., using a sequential forward search. A set of different classifiers is then tested during (supervised/unsupervised) training and the best performing features, feature-selection steps and classifiers might be used for future predictions.
Niemann et al. (
Conclusion
Current 4D flow MRI acquisitions are constrained by their scan time, spatio-temporal resolution, and SNR, limiting their accuracy and clinical application. Semi-automatic post-processing steps, including phase corrections and segmentation for vessel delineation are time-consuming and in need for automation. This review shows various ways of accelerating image reconstruction times and post-processing tasks using ML, when compared to the current state-of-the-art approaches. Code and data have been made publicly available for many ML applications reviewed for this article (as summarized in Table 1), which supports their reproducibility, applicability and development. A table summarizing all papers reviewed and their technical details can be found in the Supplementary Table 1.
TABLE 1
| References | Topic | Code |
| Vishnevsky et al. ( | Reconstruction of undersampled Cartesian 4D flow MRI data (aorta) | https://codeocean.com/capsule/0115983/tree |
| Haji-Valizadeh et al. ( | Reconstruction of radial 2D flow MRI data (aorta) | https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/N97M6H |
| Kim et al. ( | Fast 4D flow MRI by estimating velocity maps from 3-point encoding | https://github.com/uwmri/ThreePoint4DFlow |
| Ferdian et al. ( | 4D flow MRI super-resolution framework | https://github.com/EdwardFerdian/4DFlowNet |
| Kissas et al. ( | 1D flow physics informed DNN | https://github.com/PredictiveIntelligenceLab/1DBloodFlowPINNs |
| Ferdian et al. ( | WSS estimation from 4D flow MRI | https://github.com/EdwardFerdian/WSSNet |
| Berhane et al. ( | Anti-aliasing correction of 4D flow MRI data | https://github.com/hberhane/4D-flow-Velocity-Aliasing-CNN |
| Bratt et al. ( | Segmentation on 2D flow MRI data | https://github.com/akbratt/PC_AutoFlow |
| Tsou et al. ( | Segmentation on 4D flow MRI data | Uses MultiResUNet from ( https://github.com/nibtehaz/MultiResUNet |
| Corrado et al. ( | Automatic measurement plane selection on 4D flow MRI data | https://github.com/pcorrado/DL-Vessel-Localization |
| Corrado et al. ( | Ventricular segmentation on 4D flow MRI data | Using the FCN from ( https://github.com/baiwenjia/ukbb_cardiac |
| Garrido-Oliver et al. ( | 3D segmentation and landmark detection 4D flow MRI data (aorta) | Uses the nnU-Net ( https://github.com/MIC-DKFZ/nnUNet Reinforcement learning and landmark detection: https://github.com/CardiovascularImagingVallHebron/4D_flow_landmark_detection |
Available code for all original research papers screened for this review.
In the future, it will be essential that accurate cardiovascular 4D flow MRI can be performed in a single, fast scan. That includes an easy choice of VENCs (by retrospective correction of anti-aliasing and phase offsets) and spatio-temporal resolutions that might be increased by super-resolution approaches retrospectively to the scan and for vessels with slow flow and small geometries. It is important, that the analysis of the data is performed in an automated, operator independent and robust way, to allow accurate assessment of biomarkers such as peak velocities and WSS for diagnosis and clinical decision making. Classification of disease by 4D flow MRI-derived biomarkers has the potential to be reinforced by ML technologies.
Statements
Author contributions
EP conceptualizing of the manuscript, literature research for manuscripts included in the review, and manuscript writing. PO, BJ, and JB conceptualizing of the manuscript, technical feedback and discussion, and manuscript reviewing. AH and CG clinical feedback and discussion and manuscript reviewing. All authors contributed to the article and approved the submitted version.
Funding
This study was supported by funding received from the Swiss National Science Foundation (grant #PCEFP2_194296) and the Swiss Heart Foundation (grant #FF18054).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2022.1052068/full#supplementary-material
Supplementary Table 1All papers reviewed and their technical details.
References
1.
FirminDNGatehousePDKonradJPYangGZKilnerPJLongmoreDB.Rapid 7-dimensional imaging of pulsatile flow.Proceedings of computers in cardiology conference.London: IEEE (1993). p. 353–6.
2.
WigstromLSjoqvistLWranneB.Temporally resolved 3D phase-contrast imaging.Magn Reson Med. (1996) 36:800–3. 10.1002/mrm.1910360521
3.
WigströmLEbbersTFyreniusAKarlssonMEngvallJWranneBet alParticle trace visualization of intracardiac flow using time-resolved 3D phase contrast MRI.Magn Reson Med. (1999) 799:793–9. 10.1002/(SICI)1522-2594(199904)41:4<793::AID-MRM19>3.0.CO;2-2
4.
KozerkeSHasenkamJMPedersenEMBoesigerP.Visualization of flow patterns distal to aortic valve prostheses in humans using a fast approach for cine 3D velocity mapping.J Magn Reson Imaging. (2001) 13:690–8.
5.
MarklMChanFAlleyMWeddingKDraneyMElkinsCet alTime-resolved three-dimensional phase-contrast MRI.J Magn Reson Imaging. (2003) 17:499–506. 10.1002/jmri.10272
6.
HopeMMeadowsAHopeTOrdovasKSalonerDReddyGet alClinical evaluation of aortic coarctation with 4D flow MR imaging.J Magn Reson Imaging. (2010) 31:711–8. 10.1002/jmri.22083
7.
HsiaoATariqUAlleyMTLustigMVasanawalaSS.Inlet and outlet valve flow and regurgitant volume may be directly and reliably quantified with accelerated, volumetric phase-contrast MRI.J Magn Reson Imaging. (2015) 41:376–85. 10.1002/jmri.24578
8.
FeneisJKyubwaEAtianzarKChengJAlleyMVasanawalaSet al4D flow MRI quantification of mitral and tricuspid regurgitation: reproducibility and consistency relative to conventional MRI.J Magn Reson Imaging. (2018) 48:1147–58. 10.1002/jmri.26040
9.
AdriaansBPWestenbergJJCauterenYJGerretsenSElbazMSBekkersSCet alClinical assessment of aortic valve stenosis: comparison between 4D flow MRI and transthoracic echocardiography.J Magn Reson Imaging. (2020) 51:472–80. 10.1002/jmri.26847
10.
SchnellSAnsariSAVakilPHurleyMCarrJBatjerHet alCharacterization of cerebral aneurysms using 4D FLOW MRI.J Cardiovasc Magn Reson. (2012) 14:W2. 10.1186/1532-429X-14-S1-W2
11.
VasanawalaSSHannemanKAlleyMTHsiaoA.Congenital heart disease assessment with 4D flow MRI.J Magn Reson Imaging. (2015) 42:870–86. 10.1002/jmri.24856
12.
CallaghanFMBurkhardtBValsangiacomo BuechelERKellenbergerCJGeigerJ.Assessment of ventricular flow dynamics by 4D-flow MRI in patients following surgical repair of d-transposition of the great arteries.Eur Radiol. (2021) 31:7231–41. 10.1007/s00330-021-07813-0
13.
FidockBArcherGBarkerNElhawazAAl-MohammadARothmanAet alStandard and emerging CMR methods for mitral regurgitation quantification.Int J Cardiol. (2021) 331:316–21. 10.1016/j.ijcard.2021.01.066
14.
DyverfeldtPBissellMBarkerABolgerACarlhällCEbbersTet al4D flow cardiovascular magnetic resonance consensus statement.J Cardiovasc Magn Reson. (2015) 17:72. 10.1186/s12968-015-0174-5
15.
SjöbergPBidhultSBockJHeibergEArhedenHGustafssonRet alDisturbed left and right ventricular kinetic energy in patients with repaired tetralogy of Fallot: pathophysiological insights using 4D-flow MRI.Eur Radiol. (2018) 28:4066–76. 10.1007/s00330-018-5385-3
16.
HanQJWitscheyWFang-YenCArklesJBarkerAForfiaPet alAltered right ventricular kinetic energy work density and viscous energy dissipation in patients with pulmonary arterial hypertension: a pilot study using 4D flow MRI.PLoS One. (2015) 10:e0138365. 10.1371/journal.pone.0138365
17.
DyverfeldtPKvittingJSigfridssonAEngvallJBolgerAEbbersT.Assessment of fluctuating velocities in disturbed cardiovascular blood flow: in vivo feasibility of generalized phase-contrast MRI.J Magn Reson Imaging. (2008) 28:655–63. 10.1002/jmri.21475
18.
BinterCGülanUHolznerMKozerkeS.On the accuracy of viscous and turbulent loss quantification in stenotic aortic flow using phase-contrast MRI.Magn Reson Med. (2016) 76:191–6. 10.1002/mrm.25862
19.
van OoijPPottersWNederveenAAllenBCollinsJCarrJet almethodology to detect abnormal relative wall shear stress on the full surface of the thoracic aorta using four-dimensional flow MRI.Magn Reson Med. (2015) 73:1216–27. 10.1002/mrm.25224
20.
PottersWvan OoijPMarqueringHvanBavelENederveenAJ.Volumetric arterial wall shear stress calculation based on cine phase contrast MRI.J Magn Reson Imaging. (2015) 41:505–16. 10.1002/jmri.24560
21.
MarklMWallisWStreckerCGladstoneBVachWHarloffA.Analysis of pulse wave velocity in the thoracic aorta by flow-sensitive four-dimensional MRI: reproducibility and correlation with characteristics in patients with aortic atherosclerosis.J Magn Reson Imaging. (2012) 35:1162–8. 10.1002/jmri.22856
22.
CibisMPottersWGijsenFMarqueringHvan OoijPvanBavelEet alThe effect of spatial and temporal resolution of cine phase contrast MRI on wall shear stress and oscillatory shear index assessment.PLoS One. (2016) 11:e0163316. 10.1371/journal.pone.0163316
23.
van OoijPPottersWVNederveenAJCollinsJDCarrJCMalaisrieSet alThoracic aortic wall shear stress atlases in patients with bicuspid aortic valves.J Cardiovasc Magn Reson. (2014) 16:161. 10.1186/1532-429X-16-S1-P161
24.
DillingerHKozerkeSGuenthnerC.Direct comparison of gradient Fidelity and acoustic noise of the same MRI system at 3 T and 0.75 T.Magn Reson Med.. (2022) 88:1937–47. 10.1002/mrm.29312
25.
TsaoJBoesigerPPruessmannKP.k-t BLAST and k-t SENSE: dynamic MRI with high frame rate exploiting spatiotemporal correlations.Magn Reson Med. (2003) 50:1031–42. 10.1002/mrm.10611
26.
ChengJYAlleyMLustigMVasanawalaSPaulyJ.Variable-density radial view-ordering and sampling for time-optimized 3D Cartesian imaging.Proceedings of the ISMRM workshop on data sampling and image reconstruction.Sedona, AZ. (2013).
27.
LustigMDonohoDPaulyJM.Sparse MRI: the application of compressed sensing for rapid MR imaging.Magn Reson Med. (2007) 58:1182–95. 10.1002/mrm.21391
28.
VishnevskiyVWalheimJKozerkeS.Deep variational network for rapid 4D flow MRI reconstruction.Nat Mach Intell. (2020) 2:228–35. 10.1038/s42256-020-0165-6
29.
PruessmannKPWeigerMScheideggerMBBoesigerP.SENSE: sensitivity encoding for fast MRI.Magn Reson Med. (1999) 42:952–62. 10.1002/(SICI)1522-2594(199911)42:5<952::AID-MRM16>3.0.CO;2-S
30.
TsaoJKozerkeS.MRI temporal acceleration techniques.J Magn Reson Imaging. (2012) 36:543–60. 10.1002/jmri.23640
31.
PedersenHKozerkeSRinggaardSNehrkeKWonYK.k-t PCA: temporally constrained k-t BLAST reconstruction using principal component analysis.Magn Reson Med. (2009) 62:706–16. 10.1002/mrm.22052
32.
LustigMDonohoDSantosJPaulyJ.Compressed sensing MRI.IEEE Signal Process Mag. (2008) 25:72–82. 10.1109/MSP.2007.914728
33.
PrietoCDonevaMUsmanMHenningssonMGreilGSchaeffterTet alHighly efficient respiratory motion compensated free-breathing coronary MRA using golden-step Cartesian acquisition.J Magn Reson Imaging. (2015) 41:738–46. 10.1002/jmri.24602
34.
HanFZhouZHanEGaoYNguyenKFinnJet alSelf-gated 4D multiphase, steady-state imaging with contrast enhancement (MUSIC) using rotating cartesian K-space (ROCK): validation in children with congenital heart disease.Magn Reson Med. (2017) 78:472–83. 10.1002/mrm.26376
35.
ZhuYGuoYLingalaSLebelRLawMNayakK.GOCART: GOlden-angle CArtesian randomized time-resolved 3D MRI.Magn Reson Imaging. (2016) 34:940–50. 10.1016/j.mri.2015.12.030
36.
PeperESGottwaldLMZhangQCoolenBvan OoijPNederveenAet alHighly accelerated 4D flow cardiovascular magnetic resonance using a pseudo-spiral Cartesian acquisition and compressed sensing reconstruction for carotid flow and wall shear stress.J Cardiovasc Magn Reson. (2020) 22:7. 10.1186/s12968-019-0582-z
37.
GuTKorosecFBlockWFainSTurkQLumDet alPC VIPR: a high-speed 3D phase-contrast method for flow quantification and high-resolution angiography.Am J Neuroradiol. (2005) 26:743–9.
38.
HammernikKKlatzerTKoblerERechtMPSodicksonDKPockTet alLearning a variational network for reconstruction of accelerated MRI data.Magn Reson Med. (2018) 79:3055–71. 10.1002/mrm.26977
39.
Haji-ValizadehHGuoRKucukseymenSPaskavitzACaiXRodriguezJet alHighly accelerated free-breathing real-time phase contrast cardiovascular MRI via complex-difference deep learning.Magn Reson Med. (2021) 86:804–19. 10.1002/mrm.28750
40.
KimDJenM-LEisenmengerLBJohnsonKM.Accelerated 4D-flow MRI with 3-point encoding enabled by machine learning.Magn Reson Med. (2022). [Epub ahead of print]. 10.1002/mrm.29469
41.
FerdianESuinesiaputraADubowitzDZhaoDWangACowanBet al4DFlowNet: super-resolution 4D flow MRI using deep learning and computational fluid dynamics.Front Phys. (2020) 8:138. 10.3389/fphy.2020.00138
42.
LedigCTheisLHuszárFCaballeroJCunninghamA.Photo-realistic single image super-resolution using a generative adversarial network.Proceedings of the IEEE conference on computer vision and pattern recognition.Honolulu, HI: IEEE (2017). p. 4681–90. 10.1109/CVPR.2017.19
43.
RutkowskiDRRoldan-AlzateAJohnsonK.Enhancement of cerebrovascular 4D flow MRI velocity fields using machine learning and computational fluid dynamics simulation data.Sci Rep. (2021) 11:10240. 10.1038/s41598-021-89636-z
44.
MederoRRuedingerKRutkowskiDJohnsonKRoldán-AlzateA.In vitro assessment of flow variability in an intracranial aneurysm model using 4D flow MRI and tomographic PIV.Ann Biomed Eng. (2020) 48:2484–93. 10.1007/s10439-020-02543-8
45.
DirixPBuosoSPeperESKozerkeS.Synthesis of patient-specific multipoint 4D flow MRI data of turbulent aortic flow downstream of stenotic valves.Sci Rep. (2022) 12:16004. 10.1038/s41598-022-20121-x
46.
RaissiMPerdikarisPKarniadakisGE.Physics-informed neural networks: a deep learning framework for solving forward and inverse problems involving nonlinear partial differential equations.J Comput Phys. (2019) 378:686–707. 10.1016/j.jcp.2018.10.045
47.
BuschJGieseDWissmannLKozerkeS.Reconstruction of divergence-free velocity fields from cine 3D phase-contrast flow measurements.Magn Reson Med. (2013) 69:200–10. 10.1002/mrm.24221
48.
TögerJZahrMAristokleousNBlochKCarlssonMPerssonP.Blood flow imaging by optimal matching of computational fluid dynamics to 4D-flow data.Magn Reson Med. (2020) 84:2231–45. 10.1002/mrm.28269
49.
KissasGYangYHwuangEWitscheyWRDetreJA.Machine learning in cardiovascular flows modeling: predicting arterial blood pressure from non-invasive 4D flow MRI data using physics-informed neural networks.Comput Methods Appl Mech Eng. (2020) 358:112623. 10.1016/j.cma.2019.112623
50.
FathiMPerez-RayaIBaghaieABergPJanigaGArzaniAet alSuper-resolution and denoising of 4D-flow MRI using physics-informed deep neural nets.Comput Methods Programs Biomed. (2020) 197:105729. 10.1016/j.cmpb.2020.105729
51.
ShitSZimmermannJEzhovIPaetzoldJSanchesAPirklCet alSRflow: deep learning based super-resolution of 4D-flow MRI data.Front Artif Intell. (2022) 5:928181. 10.3389/frai.2022.928181
52.
StalderAFRusseMFFrydrychowiczABockJHennigJMarklM.Quantitative 2D and 3D phase contrast MRI: optimized analysis of blood flow and vessel wall parameters.Magn Reson Med. (2008) 60:1218–31. 10.1002/mrm.21778
53.
PottersWMarqueringHAVanBavelENederveenAJ.Measuring wall shear stress using velocity-encoded MRI.Curr Cardiovasc Imaging Rep. (2014) 7:9257. 10.1007/s12410-014-9257-1
54.
FerdianEDubowitzDJMaugerCAWangAYoungAA.WSSNet: aortic wall shear stress estimation using deep learning on 4D flow MRI.Front Cardiovasc Med. (2022) 8:769927. 10.3389/fcvm.2021.769927
55.
YouSMasutaniEAlleyMVasanawalaSTaubPLiauJet alDeep learning automated background phase error correction for abdominopelvic 4D flow MRI.Radiology. (2022) 302:584–92. 10.1148/radiol.2021211270
56.
JenkinsonM.Fast, automated, N-dimensional phase-unwrapping algorithm.Magn Reson Med. (2003) 49:193–7. 10.1002/mrm.10354
57.
UntenbergerMHüllebrandMTautzLJosephAVoitDMerboldtKet alSpatiotemporal phase unwrapping for real-time phase-contrast flow MRI.Magn Reson Med. (2015) 74:964–70. 10.1002/mrm.25471
58.
XiangQ-S.Temporal phase unwrapping for CINE velocity imaging.J Magn Reson Imaging. (1995) 5:529–34. 10.1002/jmri.1880050509
59.
SalfityMFHuntleyJMGravesMJMarklundOCusackRBeauregardDA.Extending the dynamic range of phase contrast magnetic resonance velocity imaging using advanced higher-dimensional phase unwrapping algorithms.J R Soc Interface. (2006) 3:415–27. 10.1098/rsif.2005.0096
60.
LoecherMSchraubenEJohnsonKMWiebenO.Phase unwrapping in 4D MR flow with a 4D single-step laplacian algorithm.J Magn Reson Imaging. (2016) 43:833–42. 10.1002/jmri.25045
61.
BerhaneHScottMBBarkerAMcCarthyPAveryRAllenBet alDeep learning–based velocity antialiasing of 4D-flow MRI.Magn Reson Med. (2022) 88:449–63. 10.1002/mrm.29205
62.
ÇiçekÖAbdulkadirALienkampSSBroxTRonnebergerO.3D U-Net: learning dense volumetric segmentation from sparse annotation. In: OurselinSJoskowiczLSabuncuMUnalGWellsWeditors. Medical image computing and computer-assisted intervention – MICCAI 2016.Cham: Springer (2016). p. 424–32. 10.1007/978-3-319-46723-8_49
63.
BrattAKimJPollieMBeecyATehraniNCodellaNet alMachine learning derived segmentation of phase velocity encoded cardiovascular magnetic resonance for fully automated aortic flow quantification.J Cardiovasc Magn Reson. (2019) 21:1. 10.1186/s12968-018-0509-0
64.
GarciaJBeckieKHassanabadAFSojoudiAWhiteJA.Aortic and mitral flow quantification using dynamic valve tracking and machine learning: prospective study assessing static and dynamic plane repeatability, variability and agreement.JRSM Cardiovasc Dis. (2021) 10:2048004021999900. 10.1177/2048004021999900
65.
TsouCChengYHuangCChenJChenWChaiJet alUsing deep learning convolutional neural networks to automatically perform cerebral aqueduct CSF flow analysis.J Clin Neurosci. (2021) 90:60–7. 10.1016/j.jocn.2021.05.010
66.
IbtehazNRahmanMS.MultiResUNet: rethinking the U-Net architecture for multimodal biomedical image segmentation.Neural Netw. (2020) 121:74–87. 10.1016/j.neunet.2019.08.025
67.
BerhaneHScottMElbazMJarvisKMcCarthyPCarrJet alFully automated 3D aortic segmentation of 4D flow MRI for hemodynamic analysis using deep learning.Magn Reson Med. (2020) 84:2204–18. 10.1002/mrm.28257
68.
Garrido-OliverJAvilesJCórdovaMDux-SantoyLRuiz-MuñozATeixido-TuraGet alMachine learning for the automatic assessment of aortic rotational flow and wall shear stress from 4D flow cardiac magnetic resonance imaging.Eur Radiol. (2022) 32:7117–27. 10.1007/s00330-022-09068-9
69.
IsenseeFJaegerPFKohlSAAPetersenJMaier-HeinKH.nnU-Net: a self-configuring method for deep learning-based biomedical image segmentation.Nat Methods. (2021) 18:203–11. 10.1038/s41592-020-01008-z
70.
MnihVKavukcuogluKSilverDRusuAVenessJBellemareMet alHuman-level control through deep reinforcement learning.Nature. (2015) 518:529–33. 10.1038/nature14236
71.
KimH-LKimS-H.Pulse wave velocity in atherosclerosis.Front Cardiovasc Med. (2019) 6:41. 10.3389/fcvm.2019.00041
72.
WentlandALGristTMWiebenO.Review of MRI-based measurements of pulse wave velocity: a biomarker of arterial stiffness.Cardiovasc Diagn Ther. (2014) 4:193–206.
73.
RogersWJHuYLCoastDVidoDAKramerCMPyeritzREet alAge-Associated Changes in Regional Aortic Pulse Wave Velocity.J Am Coll Cardiol. (2001) 38:1123–9. 10.1016/S0735-1097(01)01504-2
74.
MaYChoiJHourlier-FargetteAXueYChungHLeeJet alRelation between blood pressure and pulse wave velocity for human arteries.Proc Natl Acad Sci USA. (2018) 115:11144–9. 10.1073/pnas.1814392115
75.
KozerkeSScheideggerMBPedersenEMBoesigerP.Heart motion adapted cine phase-contrast flow measurements through the aortic valve.Magn Reson Med. (1999) 42:970–8. 10.1002/(SICI)1522-2594(199911)42:5<970::AID-MRM18>3.0.CO;2-I
76.
BustamanteMViolaFEngvallJCarlhällC-JEbbersT.Automatic time-resolved cardiovascular segmentation of 4D flow MRI using deep learning.J Magn Reson Imaging. (2022). [Epub ahead of print]. 10.1002/jmri.28221
77.
BustamanteMPeterssonSErikssonJAlehagenUDyverfeldtPCarlhällCet alAtlas-based analysis of 4D flow CMR: automated vessel segmentation and flow quantification.J Cardiovasc Magn Reson. (2015) 17:87. 10.1186/s12968-015-0190-5
78.
CorradoPAWentlandALStarekovaJDhyaniAGossKWiebenO.Fully automated intracardiac 4D flow MRI post-processing using deep learning for biventricular segmentation.Eur Radiol. (2022) 32:5669–78. 10.1007/s00330-022-08616-7
79.
BaiWSinclairMTarroniGOktayORajchlMVaillantGet alAutomated cardiovascular magnetic resonance image analysis with fully convolutional networks.J Cardiovasc Magn Reson. (2018) 20:65. 10.1186/s12968-018-0471-x
80.
CorradoPASeiterDPWiebenO.Automatic measurement plane placement for 4D Flow MRI of the great vessels using deep learning.Int J Comput Assist Radiol Surg. (2022) 17:199–210. 10.1007/s11548-021-02475-1
81.
HeKZhangXRenSSunJ.Deep Residual Learning for Image Recognition.2016 IEEE conference on computer vision and pattern recognition (CVPR).Las Vegas, NV: IEEE (2016). p. 770–8. 10.1109/CVPR.2016.90
82.
ZhuJ-YParkTIsolaPEfrosAA.Unpaired image-to-image translation using cycle-consistent adversarial networks.Proceedings of the IEEE international conference on computer vision.Venice: IEEE (2017). p. 2223–32. 10.1109/ICCV.2017.244
83.
WolterinkJMDinklaAMSavenijeMHFSeevinckPRvan den BergCATIšgumI.Deep MR to CT synthesis using unpaired data. In: TsaftarisSGooyaAFrangiAPrinceJeditors. International workshop on simulation and synthesis in medical imaging.Cham: Springer (2017). p. 14–23. 10.1007/978-3-319-68127-6_2
84.
BustamanteMViolaFCarlhällC-JEbbersT.Using deep learning to emulate the use of an external contrast agent in cardiovascular 4D flow MRI.J Magn Reson Imaging. (2021) 54:777–86. 10.1002/jmri.27578
85.
NiemannUNeogABehrendtBLawonnKGutberletMSpiliopoulouMet alCardiac cohort classification based on morphologic and hemodynamic parameters extracted from 4D PC-MRI data.arXiv. [Preprint]. (2020). Available online at: https://arxiv.org/abs/2010.05612 (accessed September 15, 2022).
86.
FrancoPSoteloJGualaADux-SantoyLEvangelistaARodríguez-PalomaresJet alIdentification of hemodynamic biomarkers for bicuspid aortic valve induced aortic dilation using machine learning.Comput Biol Med. (2022) 141:105147. 10.1016/j.compbiomed.2021.105147
Summary
Keywords
4D flow cardiovascular magnetic resonance, 4D flow, four-dimensional flow imaging, artificial intelligence, machine learning (ML)
Citation
Peper ES, van Ooij P, Jung B, Huber A, Gräni C and Bastiaansen JAM (2022) Advances in machine learning applications for cardiovascular 4D flow MRI. Front. Cardiovasc. Med. 9:1052068. doi: 10.3389/fcvm.2022.1052068
Received
23 September 2022
Accepted
22 November 2022
Published
09 December 2022
Volume
9 - 2022
Edited by
Claudia Prieto, King’s College London, United Kingdom
Reviewed by
Julio Sotelo, Universidad de Valparaíso, Chile; Angela Lungu, Technical University of Cluj-Napoca, Romania
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Copyright
© 2022 Peper, van Ooij, Jung, Huber, Gräni and Bastiaansen.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Eva S. Peper, evaspeper@gmail.com
This article was submitted to Cardiovascular Imaging, a section of the journal Frontiers in Cardiovascular Medicine
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