4.7 Article

Improved DTI registration allows voxel-based analysis that outperforms Tract-Based Spatial Statistics

Journal

NEUROIMAGE
Volume 94, Issue -, Pages 65-78

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2014.03.026

Keywords

DTI; Fractional Anisotropy; Voxel-based analysis; VBM; TBSS; Registration

Funding

  1. Alexander Family Alzheimer's Disease Research Professorship of the Mayo Foundation, USA
  2. Robert H. and Clarice Smith Alzheimer's Disease Research Program of the Mayo Foundation, USA
  3. NIH/National Institute on Aging [R01 AG011378, RO1 AG041851, R01 AG040042, U01 AG024904, U01 AG006786, P50 AG016574, C06 RR018898]
  4. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  5. National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering
  6. Canadian Institutes of Health Research
  7. NIH [P30 AG010129, K01 AG030514]

Ask authors/readers for more resources

Tract-Based Spatial Statistics (TBSS) is a popular software pipeline to coregister sets of diffusion tensor Fractional Anisotropy (FA) images for performing voxel-wise comparisons. It is primarily defined by its skeleton projection step intended to reduce effects of local misregistration. A white matter skeleton is computed by morphological thinning of the inter-subject mean FA, and then all voxels are projected to the nearest location on this skeleton. Here we investigate several enhancements to the TBSS pipeline based on recent advances in registration for other modalities, principally based on groupwise registration with the ANTS-SyN algorithm. We validate these enhancements using simulation experiments with synthetically-modified images. When used with these enhancements, we discover that TBSS's skeleton projection step actually reduces algorithm accuracy, as the improved registration leaves fewer errors to warrant correction, and the effects of this projection's compromises become stronger than those of its benefits. In our experiments, our proposed pipeline without skeleton projection is more sensitive for detecting true changes and has greater specificity in resisting false positives from misregistration. We also present comparative results of the proposed and traditional methods, both with and without the skeleton projection step, on three real-life datasets: two comparing differing populations of Alzheimer's disease patients to matched controls, and one comparing progressive supranuclear palsy patients to matched controls. The proposed pipeline produces more plausible results according to each disease's pathophysiology. (C) 2014 The Authors. Published by Elsevier Inc.

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