About the cardiovascular MRI research group

The cardiovascular magnetic resonance imaging (MRI) group, under the direction of senior scientist Dr. Graham Wright, is part of the physical sciences platform and the cardiac research program at Sunnybrook Research Institute.
Diseases of the heart and circulation are a major cause of mortality in the western world. During the last 3 decades, the cardiovascular MRI group has focused its research on improving the diagnosis and assessment of cardiovascular diseases, including ischemic and congenital heart disease, and neurovascular and peripheral vascular disease, and on characterizing blood supply associated with cancers, primarily using MRI.
Interventional guidance provides new possibilities to further help in the treatment of patients with cardiac disease. Advances in X-ray, ultrasound, optical and MR-imaging and catheter-based sensors will be integrated to facilitate the following:
- Novel revascularization methods
- Gene and stem cell therapies
- Electrophysiological interventions
- Minimally invasive surgery
We also work to provide the early feedback on success critical to rapid outcome evaluation.
Areas of focus
Sunnybrook Research Institute’s cardiovascular MRI research group focuses on the following areas:

Collaborators for clinical translation projects include GE, Siemens, Circle, and Vista.ai.
Ongoing Projects:
- Image quality evaluation with cardiac implantable electronic devices (Lead: Calder Sheagren)
- Cardiac ablation lesion evaluation in patients with arrhythmias (Lead: Terenz Escartin)
- Evaluation of cardiac scan efficiency using an AI-assisted protocol (Lead: Labonny Biswas)
The focus of this project is predictions of endovascular procedural success and long-term clinical outcomes in critical limb ischemia patients.
We address gaps in knowledge about how to select patients for percutaneous vascular interventions. This study characterizes the superficial femoral artery chronic total occlusion using a novel MRI protocol, identifying imaging biomarkers of hard vs soft peripheral arterial lesion components, which impact procedure approach.
This is an ongoing collaboration with Houston Methodist Hospital.
Excitement surrounds the use of stem cells, since these cells can potentially become functional cells of any given tissue. Stem cells implanted to a damaged area of the heart may be able to fully replace the damaged area in all the necessary aspects.
This project requires the ability to:
- Visualize the catheter needed to deliver the stem cells
- Image (in real-time) the progress of the catheter movement and maintain knowledge of its orientation
- Study the function in the neighbourhood of the cells
- Characterize the general functions of the tissue such as wall motion recovery, perfusion, viability, proliferation and differentiation
Ongoing projects:
- MR-based myocardial tissue characterization in a regenerative model (Lead: Moses Cook)
Arrhythmias associated with heart attacks can lead to open-heart surgery, which involves slicing up the heart muscle to eliminate the irregular heart contraction. To reduce the severity of intervention, we are studying muscle ablation via radio frequency (RF) heating and pulsed fields.
This study involves the ability to observe the delivery of the ablation to the desired place and imaging the ablation lesion.
Ongoing projects:
- Evaluating ablation therapies of cardiac arrhythmias using MRI biomarkers (Lead: Terenz Escartin)
- Catheter device tracking and visualization for MRI interventional guidance of arrhythmia ablations (Lead: Jay Patel)
MR Physics
Nuclear magnetic resonance (NMR), a property of atoms first observed by Bloch [1] and Purcell [2] in 1946, has proven to be an informative technique in many fields of study, particularly in chemistry and physics. The magnetic resonance signal is very rich in measurable characteristics – including initial strength, frequency of oscillation, and rate of recovery and decay – that reflect the nature of a population of atoms, the structure of their environment, and the way in which the atoms interact with this environment. Furthermore, one can manipulate the external magnetic environment in space and time to modify the NMR signal without significantly affecting material structure.
Relatively recently, magnetic resonance was extended to the in vivo study of human anatomy. This was made possible by new, practical methods for exciting signal from limited volumes [3], and for generating spatial maps of this signal [4]. Relying primarily on the differential decay and recovery characteristics of the proton NMR signal (generally termed relaxation behavior), this technology can generate images with high contrast among various soft tissues and organs. As a result, magnetic resonance imaging (MRI) has become the modality of choice in many diagnostic studies of the head, spine, and joints. With ongoing developments to improve the image quality, acquisition speed and quantitative accuracy of related measures of local signal characteristics, the range of clinical applications for MRI continues to expand rapidly.
The nature of the data produced with MRI is, in many ways, well-suited to subsequent image analysis. Specifically: (i) many different organs can be distinguished with the flexible soft tissue contrast; (ii) resolution can be tailored to specific applications and noise is generally well behaved; (iii) signal can be resolved in the three spatial dimensions to sub-millimeter levels; (iv) one can resolve temporal signal changes at the sub-second level; and (v) one can obtain multiple measurements of the same volume element with different contrast characteristics. The vast volume of data alone often demands computer image analysis for interpretation and display.
Areas of research in image analysis include methods for image segmentation [35,36,37] and registration [37,38]. Image segmentation facilitates (i) volume estimation for characterizing disease (ejection fraction in the heart, tumor volumes), (ii) isolation of a tissue of interest from a three-dimensional data set, notably for the display of vascular anatomy, and (iii) multiple image registration through the identification of common landmarks in the images. Registration facilitates (i) temporal signal analysis of a specified volume within the same study, (ii) comparative studies of the same patient over multiple studies perhaps with data of different contrast weightings or even data from different imaging modalities, and (iii) comparative studies of anatomy across multiple individuals.
The task of image analysis is simplified greatly when attention is paid to the nature of the basis images. As noted in the next section, image sequence parameters can be selected to maximize contrast between tissues, facilitating segmentation. Acquisition can be synchronized to motion or priority can be given to imaging speed to reduce the demands on registration algorithms. Similarly, registration of multiple images with different contrasts is aided by acquiring lines of k-space from the different images in a time-interleaved manner. For segmentation, image resolution should be selected to minimize the difficulties associated with partial voluming, where multiple tissues are present in the same voxel, based on the sizes of the structures of interest. Finally, the additive, Gaussian nature of the noise can be exploited to optimize classification strategies in segmentation; as a caveat, the noise takes on a Rician distribution in magnitude images most often used for segmentation as a result of the magnitude operation.
Signal processing tools are fundamental to MRI, from the design of acquisition strategies through to the analysis of the resulting images. Linear systems theory and digital filter design are used to spatially localize the signal of interest through selective excitation. Data acquisition occurs in the spatial frequency (k-space) domain where sampling theory determines resolution and field of view. Strategies for reducing image artifacts are often best developed in this domain. Image reconstruction involves fast multi-dimensional Fourier transforms, often preceded by data interpolation, re-sampling, and apodization. The resulting large digital data sets lend themselves to computer image analysis. Considerations for image analysis either performed by the computer or an expert observer begin with appropriate selection of acquisition parameters; there is a great deal of flexibility in trading off SNR and resolution and maximizing contrast between tissues of interest at this stage. As the quality of the data continues to improve with better hardware, imaging sequences, and analysis tools, new clinical applications are being developed for this very flexible, non-invasive modality. With these applications come greater challenges for the underlying signal processing.
- F. Bloch, “Nuclear induction,” Physical Review, vol. 70, pp. 460–473, 1946.
- E. Purcell, H. Torrey, and R. Pound, “Resonance absorption by nuclear magnetic moments in a solid,” Physical Review, vol. 69, pp. 37–38, 1946.
- A. Garroway, P. Grannell, and P. Mansfield, “Image formation in NMR by a selective irradiative pulse,” J. Phys. C: Solid State Phys., vol. 7, pp. L457–L462, 1974.
- P. Lauterbur, “Image formation by induced local interactions: Examples employing nuclear magnetic resonance,” Nature, vol. 242, pp. 190–191, 1973.
- E. Hahn, “Spin echoes,” Physical Review, vol. 80, pp. 580–594, 1950.
- S. Conolly, D. Nishimura, and A. Macovski, “Optimal control solution to the magnetic resonance selective excitation problem,” IEEE Transactions on Medical Imaging, vol. MI-5, no. 2, pp. 106–115, 1986.
- J. Murdoch, A. Lent, and M. Kritzer, “Computer-optimized narrowband pulses for multislice imaging,” Journal of Magnetic Resonance, vol. 74, pp. 226–263, 1987.
- J. M. Pauly, P. Le Roux, D. Nishimura, and A. Macovski, “Parameter relations for the Shinnar-Le Roux RF pulse design algorithm,” IEEE Transactions on Medical Imaging, pp. 53–65, March 1991.
- J. Pauly, D. Nishimura, and A. Macovski, “A k-space analysis of small-tip-angle excitation,” Journal of Magnetic Resonance, vol. 81, pp. 43–56, 1989.
- D. B. Tweig, “The k-trajectory formulation of the NMR imaging process with applications in analysis and synthesis of imaging methods,” Medical Physics, vol. 10, no. 5, p. 610, 1983.
- A. Kumar, D. Welti, and R. R. Ernst, “NMR Fourier zeugmatography,” Journal of Magnetic Resonance, vol. 18, pp. 69–83, 1975.
- R. Bracewell, The Fourier Transform and its Applications. San Francisco: McGraw-Hill Book Company, 1978.
- J. Hennig, A. Nauerth, and H. Friedburg, “RARE imaging: a fast imaging method for clinical MR,” Magnetic Resonance in Medicine, vol. 3, pp. 823–833, 1986.
- A. Haase, “Snapshot FLASH MRI. Applications to T1, T2, and chemical-shift imaging,” Magnetic Resonance in Medicine, vol. 13, no. 1, 1990.
- P. Mansfield, “Multi-planar image formation using NMR spin echoes,” Journal of Physics C, vol. 10, pp. L55–L58, 1977.
- J. I. Jackson, C. H. Meyer, D. G. Nishimura, and A. Macovski, “Selection of a convolution function for Fourier inversion using gridding,” IEEE Transactions on Medical Imaging, vol. 10, pp. 473–478, 1991.
- C. Meyer, B. Hu, D. Nishimura, and A. Macovski, “Fast spiral coronary artery imaging,” Magn. Reson. Med., vol. 28, pp. 202–213, 1992.
- P. Bottomley, T. Foster, R. Argersinger, and L. Pfeifer, “A review of normal tissue hydrogen NMR relaxation times and relaxation mechanisms from 1-100 MHz: Dependence on tissue type, NMR frequency, temperature, species, excision, and age,” Medical Physics, vol. 11, no. 4, pp. 425–448, July/August 1984.
- E. McVeigh, M. Bronskill, and M. Henkelman, “Optimization of MR protocols: A statistical decision analysis approach,” Magnetic Resonance in Medicine, vol. 6, pp. 314–333, 1988.
- P. Bottomley, C. Hardy, R. Argersinger, and G. Allen-Moore, “A review of 1H nuclear magnetic resonance relaxation in pathology: Are T1 and T2 diagnostic?,” Medical Physics, vol. 14, pp. 1–37, Jan/Feb 1987.
- G. Wright, D. Nishimura, and A. Macovski, “Flow-independent magnetic resonance projection angiography,” Magnetic Resonance in Medicine, vol. 17, no. 1, pp. 126–140, 1991.
- R. Gronas, P. Kalman, A. Kiruluta, and G. Wright, “Protocol optimization of flow-independent angiography for peripheral vascular disease,” in Third Meeting of the Society of Magnetic Resonance, vol. 1, p. 75, August 1995.
- J. Brittain, E. Olcott, A. Szuba, P. Irarrazabal, G. Gold, G. Wright, and D. Nishimura, “Improvements for clinical 3D flow-independent peripheral angiography,” in Fourth Meeting of the Society of Magnetic Resonance, vol. 1, p. 242, April 1996.
- G. Wright, B. Hu, and A. Macovski, “Estimating oxygen saturation of blood in vivo with MRI at 1.5 T,” Journal of Magnetic Resonance Imaging, pp. 275–283, 1991.
- K. Li, G. Wright, L. Pelc, R. Dalman, J. Brittain, H. Wegmueller, D. Lin, and C. Song, “Oxygen saturation of blood in the superior mesenteric vein: In vivo verification of MR imaging measurements in a canine model,” Radiology, vol. 194, no. 2, pp. 321–326, 1995.
- H. Nyquist, “Thermal agitation of electric charge in conductors,” Physical Review, vol. 32, pp. 110–113, July 1928.
- S. Conolly, A. Macovski, and J. Pauly, “Magnetic resonance imaging: Acquisition and processing,” in Biomedical Engineering Handbook (J. Bronzino, ed.), CRC Press, Inc., 1994.
- W. Edelstein, G. Glover, C. Hardy, and R. Redington, “The intrinsic signal-to-noise ratio in NMR imaging,” Magnetic Resonance in Medicine, vol. 3, pp. 604–618, 1986.
- M. Bronskill and M. Henkelman, “Artifacts in magnetic resonance imaging,” Reviews of Magnetic Resonance in Medicine, vol. 2, no. 1, 1987.
- M. Wood and M. Henkelman, “MR image artifacts from periodic motion,” Medical Physics, vol. 12, no. 2, pp. 143–151, 1985.
- D. Bailes, D. Gilderdale, G. Bydder, A. Collins, and D. Firmin, “Respiratory ordered phase encoding (ROPE): A method for reducing respiratory motion artefacts in MR imaging,” Journal of Computer Assisted Tomography, pp. 835–838, 1985.
- M. Wood, M. Shivji, and P. Stanchev, “Planar-motion correction with use of k-space data acquired in Fourier MR imaging,” Journal of Magnetic Resonance Imaging, vol. 5, pp. 57–64, 1995.
- T. Sachs, C. Meyer, P. Irarrazabal, B. Hu, D. Nishimura, and A. Macovski, “The diminishing variance algorithm for real-time reduction of motion artifacts in MRI,” Magn. Reson. Med., vol. 34, pp. 412–422, 1995.
- P. S. Melki, R. V. Mulkern, L. P. Panych, and F. A. Jolesz, “Comparing the FAISE method with conventional dual-echo sequences,” Journal of Magnetic Resonance Imaging, vol. 1, pp. 319–326, 1991.
- H. Cline, W. Lorensen, R. Kikinis, and F. Jolesz, “Three-dimensional segmentation of MR images of the head using probability and connectivity,” Journal of Computer Assisted Tomography, vol. 14, no. 6, pp. 1037–1045, 1990.
- J. Bezdek, L. Hall, and L. Clarke, “Review of MR image segmentation techniques using pattern recognition,” Medical Physics, vol. 20, no. 4, pp. 1033–1048, 1993.
- L. Clarke, R. Vethuizen, M. Camacho, J. Heine, M. Vaidyanathan, L. Hall, R. Thatcher, and M. Silbiger, “MRI segmentation: Methods and applications,” Magnetic Resonance Imaging, vol. 13, no. 3, pp. 343–368, 1995.
- P. van den Elsen, E. Pol, and M. Viergever, “Medical image matching – a review with classification,” IEEE Engineering in Medicine and Biology, vol. 12, pp. 26–39, 1993.
Collaborations
Collaborating institutions and academic groups
- Hospital for Sick Children
- University Health Network
- University of California San Francisco
- Houston Methodist Academic Institute
- University of Ljubljana
- Amsterdam University Medical Center
Principal investigator
Members
- Terenz Escartin is investigating the capacity of MRI to improve treatment outcomes of cardiac arrhythmias using radiofrequency ablation therapy and pulsed field ablation. The overall goal is to evaluate procedural success of different cardiac ablation therapies using cardiac MRI biomarkers.
- Jay Patel‘s research focuses on advancing MRI-guided interventions by developing novel device tracking and visualization algorithms. He is working on improving lesion visualization in 3D high-resolution imaging, particularly for real-time assessments. Additionally, he is enhancing catheter tracking techniques and implementing motion correction methods for motion-resolved imaging, aimed at improving the clarity and precision of high-resolution MRI datasets during cardiac interventions.
- Moses Cook completed his H.B.Sc. degree in Biological Physics at the University of Toronto. There, he pursued research in signal analysis of the cardiovascular system. Moses is now applying these principles in his current preclinical project, myocardial tissue characterization in a regenerative model using MRI.
- Bonny Biswas worked in medical software companies and at the Hospital for Sick Children prior to joining the Wright lab. She has since worked on various projects in MR imaging and analysis. She manages development of software and pipelines related to visualization, image-guided interventions, image analysis, and reproducible research.
- Calder Sheagren joined the Wright Lab in Fall 2020 after completing a B.S. in Mathematics with Honors at the University of Chicago. Calder’s research interests in the Wright group include pulse sequence programming, image reconstruction, and imaging patients with cardiac implantable electronic devices. For more information, see https://caldersheagren.com/
Alumni
Ali Abhari, Daimler Chrysler
Kevan Anderson, private sector
Zohreh Azimi Far, Shiraz University
Howard Chen, private sector
Jin Choi, private sector
Desmond Chung, private sector
Brandon Coles, private sector
Charles Cunningham, Sunnybrook Health Sciences Centre
Andrew Derbyshire, National Institutes of Health
Jay Detsky, Sunnybrook Health Sciences Centre
Rohan Dharmakumar, Indiana University
Mitchell Doughty, private sector
Sebastian Ferguson, private sector
Roey Flor, private sector
Warren Foltz, St. Michael’s Hospital
Nilesh Ghugre, private sector
Greg Griffin, private sector
Fumin Guo, Huazhong University of Science and Technology
Arjun Gupta, University of Toronto
Fayez Habach, University of Washington
Saqeeb Hassan, private sector
Nick Hu, private sector
Rui Huang, private sector
Yuexi Huang, Sunnybrook Health Sciences Centre
Siavash Jafarpour, private sector
Brian Kates, private sector
Jae Kim, private practice
Andrew Kiruluta, Harvard University
Philippa Krahn, UC Berkeley
Garry Liu, private sector
Yingli Lu, private sector
Chris Macgowan, Hospital for Sick Children
Francois Marcotte, Montreal Heart Institute
Matthew Ng, private sector
Mike Noseworthy, McMaster University
Samuel Oduneye, private sector
Stefan Pintilie, private sector
Xiuling Qi, Sunnybrook Health Sciences Centre
Perry Radau, private sector
Nikoo Saber, University of Toronto
Moujan Saderi, Langonne Institute NYU
Adrienne Siu, private sector
Jay Soni, private sector
Jeff Stainsby, private sector
Marshall Sussman, University Health Network
Venkat Swaminathan, private sector
Jonathan Toma, Windsor Heart Institute
Michael Truong, private sector
Christie Webster, Sunnybrook Health Sciences Centre
Jill Weyers, University of Toronto
Eranga Ukwatta, University of Guelph
Robert Xu, private sector
Dingrong Yi
Nicolas Yak, private sector
Yuesong Yang
Emeli Zhang, private sector
Clinical collaborators
Idan Roifman, Sunnybrook Health Sciences Centre
Gideon Cohen, Sunnybrook Health Sciences Centre
Richard Farb, University Health Network
Stephen Fremes, Sunnybrook Health Sciences Centre
Naeem Merchant, University Health Network
Trisha Roy, Houston Methodist
Duncan Stewart, St. Michael’s Hospital
Bradley Strauss, Sunnybrook Health Sciences Centre
Shi-Joon Yoo, Hospital for Sick Children
Basic research collaborators
Haydar Celik, George Washington University
Margaret Cheng, Hospital for Sick Children
Hong Huang, University Health Network
Chris Macgowan, Hospital for Sick Children
Marshall Sussman, University Health Network
Ali Tavallaei, Toronto Metropolitan University
Mihaela Pop, Sunnybrook Health Sciences Centre