Motion-guided segmentation for cine DENSE MRI
Introduction
A number of MRI techniques have been developed to quantify myocardial motion, including myocardial tagging (Zerhouni et al., 1988, Axel and Dougherty, 1989), phase contrast (PC) velocity encoding (van Dijk, 1984, Bryant et al., 1984), and more recently, displacement encoding with stimulated echoes (DENSE) (Aletras et al., 1999). DENSE has the advantage over velocity-encoded PC of directly measuring tissue displacement instead of velocity, and the advantages over tagging of higher spatial resolution and more direct computation of displacement. Quantitative methods are potentially useful for reducing subjectivity and improving accuracy (Gotte et al., 2001) in the clinical assessment of cardiac wall motion, but their clinical use is currently limited by lack of automation.
Defining epicardial and endocardial contours is an integral step in quantifying regional cardiac wall motion. For cine DENSE (Kim et al., 2004) these contours are typically manually delineated for all cardiac phases, which is a laborious process and is currently the most time-consuming component of the cine DENSE image analysis. Automated myocardial contour detection techniques based on image intensity may not be well-suited to cine DENSE because: (1) boundaries between the myocardium and adjacent tissue (e.g. the liver) are often indiscernible based on signal magnitude; (2) a T1-related decay in signal-to-noise ratio (SNR) with time is often present; and (3) high signal is present in the blood pool of the first few frames, before it is washed out of the image plane.
A number of advances have been made towards automating image segmentation for myocardial tagging and velocity encoding (Kumar and Goldgof, 1994, Young et al., 1995, Kraitchman et al., 1995, Guttman et al., 1994, Montillo et al., 2002, Montillo et al., 2003, Wong et al., 2002, Cho and Benkeser, 2006) but no segmentation algorithm specifically tailored for cine DENSE has been developed. A segmentation method is presented here that uses tissue tracking based on the motion encoded into the phase of the cine DENSE images themselves to project individual manually-defined contours through time. The method is shown to be accurate, versatile and practical, and forms a significant step towards the automation of cine DENSE image analysis.
Section snippets
Cine DENSE MRI and tissue tracking
DENSE uses the phase of the stimulated echo to monitor myocardial motion and deformation at a pixel resolution. The magnetization is initially position encoded using two 90° radiofrequency pulses separated by a gradient pulse, which are typically applied at end-diastole. Tissue displacement that occurs between the displacement encoding pulses and subsequent data acquisition times causes a phase shift of the stimulated echo, resulting in images with pixel phase proportional to tissue
Methods
We propose using the motion encoded within the cine DENSE images to guide the segmentation process. This is achieved by using the myocardial motion trajectories to project any manually-defined portion of myocardium at one cardiac phase onto all other cardiac phases. Since the cine DENSE displacement fields all reference time t0, the initial contour(s) can be drawn on any cardiac phase. The displacement vector starting points of every pixel in the manually contoured region thus define the
Experiment and validation
The cine DENSE scans were performed on 1.5 T Siemens Sonata and Avanto scanners (Siemens Medical Systems, Erlangen, Germany). Six normal volunteers were scanned, and all subjects provided informed consent and were studied in accordance with research protocols approved by the Human Investigations Committee at the University of Virginia. Both conventional cine DENSE (Kim et al., 2004) and slice-followed cine DENSE (Spottiswoode et al., 2008) data were acquired for each volunteer, with
Results
Fig. 8b shows a typical early-systolic slice-followed cine DENSE magnitude image with a manually-drawn set of contours. Fig. 8a, c and d depict the corresponding motion-guided contours for a few cardiac phases. Note in Fig. 8a that contours are reliably projected onto the first cardiac phase, where many of the borders are indistinguishable to the human observer due to the signal from LV and RV blood.
Based on the mean of false positive and false negative area measures with manually-defined
Discussion
Both cine DENSE and velocity-encoded PC have the potential to incorporate information from magnitude and phase images to assist the segmentation process. Although velocity-encoded magnitude images are not interrupted by tag lines, they are “white blood” sequences and thus suffer from a lack of contrast between blood and myocardium. Wong et al. (2002) presented a myocardial segmentation technique where velocity fields from velocity-encoding were combined with a two-stage front propagation
Conclusion
A reliable and effective 2D segmentation method has been developed for 2D cine DENSE, where encoded myocardial motion is used to project a set of contours through time. The total user interaction in cine DENSE image analysis is thus reduced to the manual demarcation of the myocardium on a single frame. The technique is solely based on the cine DENSE phase images, but the additional use of magnitude information holds promise for further automation. A radial segmentation error metric was
Acknowledgements
This work was supported by NIH NIBIB Grant RO1 EB 001763 and NIH Fogarty International Center and NIBIB Grant R03 TW007633; the National Research Foundation of South Africa; the Medical Research Council of South Africa; Siemens Medical Solutions; Siemens Corporate Research; and the University of Cape Town.
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