PLoS ONE (Jan 2014)

Multi-contrast multi-atlas parcellation of diffusion tensor imaging of the human brain.

  • Xiaoying Tang,
  • Shoko Yoshida,
  • John Hsu,
  • Thierry A G M Huisman,
  • Andreia V Faria,
  • Kenichi Oishi,
  • Kwame Kutten,
  • Andrea Poretti,
  • Yue Li,
  • Michael I Miller,
  • Susumu Mori

DOI
https://doi.org/10.1371/journal.pone.0096985
Journal volume & issue
Vol. 9, no. 5
p. e96985

Abstract

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In this paper, we propose a novel method for parcellating the human brain into 193 anatomical structures based on diffusion tensor images (DTIs). This was accomplished in the setting of multi-contrast diffeomorphic likelihood fusion using multiple DTI atlases. DTI images are modeled as high dimensional fields, with each voxel exhibiting a vector valued feature comprising of mean diffusivity (MD), fractional anisotropy (FA), and fiber angle. For each structure, the probability distribution of each element in the feature vector is modeled as a mixture of Gaussians, the parameters of which are estimated from the labeled atlases. The structure-specific feature vector is then used to parcellate the test image. For each atlas, a likelihood is iteratively computed based on the structure-specific vector feature. The likelihoods from multiple atlases are then fused. The updating and fusing of the likelihoods is achieved based on the expectation-maximization (EM) algorithm for maximum a posteriori (MAP) estimation problems. We first demonstrate the performance of the algorithm by examining the parcellation accuracy of 18 structures from 25 subjects with a varying degree of structural abnormality. Dice values ranging 0.8-0.9 were obtained. In addition, strong correlation was found between the volume size of the automated and the manual parcellation. Then, we present scan-rescan reproducibility based on another dataset of 16 DTI images - an average of 3.73%, 1.91%, and 1.79% for volume, mean FA, and mean MD respectively. Finally, the range of anatomical variability in the normal population was quantified for each structure.