Purpose: To introduce a framework that automatically identifies regions of anatomical abnormality within anatomical MR images and uses those regions in hypothesisdriven selection of seed points for fiber tracking with diffusion tensor (DT) imaging (DTI).
Materials and Methods:Regions of interest (ROIs) are first extracted from MR images using an automated algorithm for volume-preserved warping (VPW) that identifies localized volumetric differences across groups. ROIs then serve as seed points for fiber tracking in coregistered DT images. Another algorithm automatically clusters and compares morphologies of detected fiber bundles. We tested our framework using datasets from a group of patients with Tourette's syndrome (TS) and normal controls.
Results:Our framework automatically identified regions of localized volumetric differences across groups and then used those regions as seed points for fiber tracking. In our applied example, a comparison of fiber tracts in the two diagnostic groups showed that most fiber tracts failed to correspond across groups, suggesting that anatomical connectivity was severely disrupted in fiber bundles leading from regions of known anatomical abnormality.
Conclusion:Our framework automatically detects volumetric abnormalities in anatomical MRIs to aid in generating a priori hypotheses concerning anatomical connectivity that then can be tested using DTI. Additionally, automation enhances the reliability of ROIs, fiber tracking, and fiber clustering. THE GENERAL RUBRIC of magnetic resonance imaging (MRI) subsumes various modalities of data acquisition (e.g., T1-and T2-weighted anatomical imaging, magnetic resonance spectroscopy, and diffusion tensor (DT) imaging (DTI)), each of which provides unique but complementary information about brain structure and function. Combining data from multiple MRI modalities can provide a more comprehensive view of a subject or group of subjects than can any single MRI modality. For example, anatomical T1-or T2-weighted MR images can help to identify structural boundaries within the gray matter and white matter of the human cerebrum, whereas DTI and its derived measures (e.g., fractional anisotropy [FA], apparent diffusion coefficient [ADC]) provide information about the directional organization of brain tissue that can be used to track nerve-fiber pathways. Moreover, a map of the principal directions for the diffusion of water, generated using DTI, can help to more accurately parcellate the anatomy of the corpus callosum (CC) and other white matter structures (e.g., cingulum, external capsule, and anterior thalamic radiation) (1-4) that appear homogeneous in their contrast and signal intensities in T1-or T2-weighted images.Researchers have long desired to integrate information from both modalities to provide a more comprehensive view of anatomical structure and connectivity in the human brain. The integration of T1-weighted and DT imaging data, however, faces at least two major obstacles: 1) the accurate coregistration of datasets from the two modaliti...