Abstract—We developed a general method for global conformal parameterizations based on the structure of the cohomology group of holomorphic one-forms for surfaces with or without boundaries (Gu and Yau, 2002), (Gu and Yau, 2003). For genus zero surfaces, our algorithm can find a unique mapping between any two genus zero manifolds by minimizing the harmonic energy of the map. In this paper, we apply the algorithm to the cortical surface matching problem. We use a mesh structure to represent the brain surface. Further constraints are added to ensure that the conformal map is unique. Empirical tests on magnetic resonance imaging (MRI) data show that the mappings preserve angular relationships, are stable in MRIs acquired at different times, and are robust to differences in data triangulation, and resolution. Compared with other brain surface conformal mapping algorithms, our algorithm is more stable and has good extensibility. Index Terms—Brain mapping, conformal map, landmark matching, spherical harmonic transformation. I.

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Enlarged ventricular size and/or asymmetry have been found markers for psychiatric illness, including schizophrenia. However, this morphometric feature is non-specific and occurs in many other brain diseases, and its variability in healthy controls is not sufficiently understood. We studied ventricular size and shape in 3D MRI (N=20) of monozygotic (N=5) and dizygotic (N=5) twin pairs. Left and right lateral, third and fourth ventricles were segmented from high-resolution T1w SPGR MRI using supervised classification and 3D connectivity. Surfaces of binary segmentations of left and right lateral ventricles were parametrized and described by a series expansion using spherical harmonics. Objects were aligned using the intrinsic coordinate system of the ellipsoid described by the first order expansion. The metric for pairwise shape similarity was the mean squared distance (MSD) between object surfaces. Without normalization for size, MZ twin pairs only showed a trend to have more similar lateral ventricles than DZ twins. After scaling by individual volumes, however, the pairwise shape difference between right lateral ventricles of MZ twins became very small with small group variance, differing significantly from DZ twin pairs. This finding suggests that there is new information in shape not represented by size, a property that might improve understanding of neurodevelopmental and neurodegenerative changes of brain objects and of heritability of size and shape of brain structures. The findings further suggest that alignment and normalization of objects are key issues in statistical shape analysis which need further exploration.

Statistical shape analysis has become of increasing interest to the neuroimaging community due to its potential to precisely locate morphological changes and thus potentially discriminate between healthy and pathological structures. This paper describes a combined boundary and medial shape analysis based on two different shape descriptions applied to a study of the hippocampus shape abnormalities in schizophrenia. The first shape description is the sampled boundary implied by the spherical harmonic SPHARM description. The second one is the medial shape description called M-rep. Both descriptions are sampled descriptions with inherent point correspondence. Their shape analysis is based on computing differences from an average template structure analyzed using standard group mean difference tests. The results of the global and local shape analysis in the presented hippocampus study exhibit the same patterns for the boundary and the medial analysis. The results strongly suggest that the normalized hippocampal shape of the schizophrenic group is different from the control group, most significantly as a deformation difference in the tail region.

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Knowledge about the biological variability of anatomical objects is essential for statistical shape analysis and discrimination between healthy and pathological structures. This paper describes a novel approach that incorporates the variability of an object population into the generation of a characteristic 3D shape model. The proposed shape representation is a coarse-scale sampled medial description derived from a fine-scale spherical harmonics (SPHARM) boundary description. This medial description is composed of a net of medial samples (m-rep) with fixed graph properties. The medial model is computed automatically from a predefined shape space using pruned 3D Voronoi skeletons. A new method determines the stable medial branching topology from the shape space. An intrinsic coordinate system and an implicit correspondence between shapes is defined on the medial manifold. Several studies of biological structures clearly demonstrate that the novel representation has the promise to describe shape changes in a natural and intuitive way. A new medial shape similarity study of group di#erences between Monozygotic and Dizygotic twins in lateral ventricle shape demonstrates the meaningful and powerful representation of local and global form.

We present a new framework for 3D surface object classification that combines a powerful shape description method with suitable pattern classification techniques. Spherical harmonic parameterization and normalization techniques are used to describe a surface shape and derive a dual high dimensional landmark representation. A point distribution model is applied to reduce the dimensionality. Fisher’s linear discriminants and support vector machines are used for classification. Several feature selection schemes are proposed for learning better classifiers. After showing the effectiveness of this framework using simulated shape data, we apply it to real hippocampal data in schizophrenia and perform extensive experimental studies by examining different combinations of techniques. We achieve best leave-one-out cross-validation accuracies of 93 % (whole set, N = 56) and 90 % (right-handed males, N = 39), respectively, which are competitive with the best results in previous studies using different techniques on similar types of data. Furthermore, to help medical diagnosis in practice, we employ a threshold-free receiver operating characteristic (ROC) approach as an alternative evaluation of classification results as well as propose a new method for visualizing discriminative patterns.

Computational anatomy (CA) is the mathematical study of anatomy I a I = I a BG, an orbit under groups of diffeomorphisms (i.e., smooth invertible mappings) g a G of anatomical exemplars Iaa I. The observable images are the output of medical imaging devices. There are three components that CA examines: (i) constructions of the anatomical submanifolds, (ii) comparison of the anatomical manifolds via estimation of the underlying diffeomorphisms g a G defining the shape or geometry of the anatomical manifolds, and (iii) generation of probability laws of anatomical variation P(d) on the images I for inference and disease testing within anatomical models. This paper reviews recent advances in these three areas applied to shape, growth, and atrophy.

The rapid collection of brain images from healthy and diseased subjects has stimulated the development of powerful mathematical algorithms to compare, pool and average brain data across whole populations. Brain structure is so complex and variable that new approaches in computer vision, partial differential equations, and statistical field theory are being formulated to detect and visualize disease-specific patterns. We present some novel mathematical strategies for computational anatomy, focusing on the creation of population-based brain atlases. These atlases describe how the brain varies with age, gender, genetics, and over time. We review applications in Alzheimer's disease, schizophrenia and brain development, outlining some current challenges in the field.

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