asymmetry, volume changes, etc.). Second, we obtained,courtesy of Massachusetts General Hospital’s Center forMorphometric Analysis, a set of MR images along withcorresponding hand segmentations by human experts(neuroanatomists). Although we will, in this section, refer to thishand segmentation as the “truth,” this is in fact a somewhatunfair procedure since the human experts clearly use moreinformation than simply image data. More specifically, there areoccasions in which the human experts have placed regionboundaries where we, as nonexperts, would not (for examplealong the bilateral symmetry line separating the two parts of thelateral ventricle when no such separation is visible in the imagedata). As such, some degree of discrepancy between oursegmentation algorithm and the human segmentation is to beexpected. Furthermore, in the discussions that follow, we willquantify our results with respect to two criteria: the handsegmentation results from human experts, and the handsegmentation results (as obtained by nonexperts ofneuroanatomy) based exclusively on image data (referred to asthe “image-based manual segmentation” below).Figure 4 shows the results of our algorithm as applied to theextraction of the lateral ventricles via an actual MR image. Theatlas used in the processing was derived from another brain.Figure 4(a) shows a close-up of a T 1 MR image of the region ofinterest. Figure 4(b) shows a dimmed version of the samegrayscale MR image, but with the human expert segmentationsuperimposed. Figure 4(c) shows a similar view, but oursegmentation superimposed. In all, the algorithm seems to havedone a reasonable job of delineating the relevant features,although both expert segmentation and our algorithm missed --in a purely image intensity sense -- the very tip of the ventricles.Figure 5 shows the same information as Figure 4, but as appliedto the caudate. In this case, the algorithm did not segment thetail structure (bottom of the caudate) that is present in thehuman expert segmentation. And in fact, this tail structure isvery difficult to identify with the untrained eye. The algorithmdid, however, err by converging to the dominant edge at the topof the ventricle instead of the lower contrast edge that separatesthe ventricle from the caudate.Based on our (small) sample of brains with two-dimensionalcoronal slices and corresponding human expert segmentations,the result of our algorithm is summarized in Table 1. Specifically,Table 1 shows the average absolute error in the ventricular andcaudate areas across all slices and all brains in our sample. Theerrors are expressed in percentages, computed with respect to thearea of the “true” segmentations performed by humans. The firstcolumn of data shows our error with respect to the human expertsegmentation; the second data column shows our error withFigure 4. Segmentation algorithm applied to MR data of ventricles: (a) MR T 1 ; (b) hand segmentation results byneuroanatomists superimposed on the MR image; (c) the result of our segmentation algorithm.Figure 5. Segmentation algorithm applied to MR data of the caudate: (a) MR T 1 ; (b) hand segmentation resultsby neuroanatomists superimposed on the MR image; (c) the result of our segmentation algorithm.Segmentation of MR Images Using Curve Evolution and Prior7
Table 1. A summary of segmentation algorithm error with respectto human segmentation.respect to an independent image-based manual segmentation bysomeone with knowledge only of image processing and not ofneuroanatomy.As Table 1, shows, there is a significant difference in performancewhen comparing the algorithm to human expert segmentationversus an image-only-based human segmentation. Aperformance of 20-percent error as compared to human experts,while not great, was also not unexpected given the extent towhich such segmentations deviated from image data. A 5-percent error as compared to nonexpert segmentation, however,reassured us that the algorithm is properly exploiting the imagefeatures as well as the prior information in deriving the resultingsegmentations.Concluding RemarksIn summary, we have presented a method for segmentinganatomical structures using only minimal operator interactions.This method achieves good performance when compared tohuman segmentations based solely on image intensities. Theproposed formulation can be a powerful new tool in assistingscientists and clinicians in evaluating patient ailments andmaking volumetric measurements. This formulation continuesthe work of numerous researchers in the field of variationalimage processing and uses a new formulation recently describedby Shah (Ref. [12]) for combining into a single functional theability to perform nonlinear diffusion, estimate an edge strengthfunction, perform curve evolution, and ultimately obtain asegmentation. When applied to the problems of delineating thelateral ventricles and caudate, the formulation yieldswell-behaved curves that capture the essence of the structures ofinterest, while remaining robust with respect to the uneven biasfield effects, low-contrast edges, and even shape distortions. Thistool is sufficiently general to assist the human operator in avariety of scenarios, including segmentation from a predefinedatlas, as well as segmentation of a structure of interest using anearlier segmentation as the reference. In particular, although wehave demonstrated our approach using a predefined atlas, ourempirical tests have shown great robustness when segmentingone slice of MR data by bootstrapping from the segmentation ofthe previous slice.Two significant problems still persist in our current formulation.First, the method is computationally intensive. Even when theimage is limited to the region of interest (e.g., the areacontaining the lateral ventricles and caudate), it takes severalminutes to estimate the edge strength function as well as performthe curve evolution using a Sun Sparc20 workstation. Ideally, wewould like to achieve near real time so that the clinician canreceive immediate quantitative results. Second, at present, themethod does not perform well in sharp corners due to the factthat curve evolution evolves with a velocity proportional tocurvature. This problem is particularly acute near the horns ofthe lateral ventricles where the corners can be quite sharp. Weare currently working on a remedy for this problem.AcknowledgmentWe gratefully acknowledge Drs. Kennedy and Worth ofMassachusetts General Hospital for providing the MR imagery.We are also indebted to Anthony Sacramone for his able support,and to David Suh for his programming support on the thin-platewarping algorithm.References[1] Filipek, P., C. Richelme, D. Kennedy, and V. Caviness, “TheYoung Adult Human Brain: an MRI-Based MorphometricAnalysis,” Cereb. Cortex, 4(4), July-August 1994.[2] Giedd, F., J. Snell, N. Lange, J. Rajapakse, B. Casey, P. Kozuch,A. Vaituzis, Y. Vauss, S. Hamburger, D. Kaysen, and J.Raporport, “Quantitative Magnetic Resonance Imaging ofHuman Brain Development: Ages 4 - 18,” Cereb Cortex, 6(4),July-August 1996.[3] Jernigan, T., G. Press, and J. Hesselink, “Methods forMeasuring Brain Morphologic Features on MagneticResonance Images,” Arch. Neurology, 47, January 1990.[4] Sullivan, E., L. Marsh, D. Mathalon, K. Lim, and A.Pfefferbaum, “Age-Related Decline in MRI Volumes ofTemporal Lobe Gray Matter But Not Hippocamus,”Neurobiol. Aging, 16(4), July-August 1995.[5] Golden, N., M. Ashtari, M. Kohn, M. Patel, M. Jacobson, A.Fletcher, and I. Shenker, “Reversibility of Cerebral VentricularEnlargement in Anorexia Nervosa, Demonstrated byQuantitative Magnetic Resonance Imaging,” J. Pediatrics,128(2), February 1996.[6] Castellanos, F., J. Giedd, W. Marsh, S. Hamburger, A. Vaituzis,D. Dickstein, S. Sarfatti, Y. Vauss, J. Snell, N. Lange, D.Segmentation of MR Images Using Curve Evolution and Prior8
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monitoring of space structures and
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