Quantitative Diffusion Tensor Imaging in Amyotrophic Lateral Sclerosis: Revisited

Caroline A. Sage, Wim Van Hecke, Ronald Peeters, Jan Sijbers, Wim Robberecht, Paul Parizel, Guy Marchal, Alexander Leemans, Stefan Sunaert

Research output: Contribution to journalArticlepeer-review

117 Citations (Scopus)


Voxel-based analyses (VBA) are increasingly being used to detect white matter abnormalities with diffusion tensor imaging (DTI) in different types of pathologies. However, the validity, specificity, and sensitivity of statistical inferences of group differences to a large extent depend on die quality of die spatial normalization of the DTI images. Using high-dimensional nonrigid coregistration techniques that are able to align both the spatial and orientational diffusion information and incorporate appropriate templates that contain this complete DT information may improve this quality. Alternatively, a hybrid technique such as tract-based spatial statistics (TBSS) may improve the reliability of the statistical results by generating voxel-wise statistics without the need for perfect image alignment and spatial smoothing. In this study, we have used (1) a coregistration algorithm that was optimized for coregistration of DTI data and (2) a population-based DTI atlas to reanalyze our previously published VBA, which compared the fractional anisotropy and mean diffusivity maps of patients with amyotrophic lateral sclerosis (ALS) with those of healthy controls. Additionally, we performed a complementary TBSS analysis to improve our understanding and interpretation of the VBA results. We demonstrate that, as the overall variance of the diffusion properties is lowered after normalizing the DTI data with such recently developed techniques (VBA using our own optimized high-dimensional nonrigid coregistration and TBSS), more reliable voxel-wise statistical results can be obtained than had previously been possible, with our VBA and TBSS yielding very similar results. This study provides support for the view of ALS as a multisystem disease, in which the entire frontotemporal lobe is implicated. Hum Brain Mapp 30:3657-3675, 2009. (C) 2009 Wiley-Liss Inc.

Original languageEnglish
Pages (from-to)3657-3675
Number of pages19
JournalHuman Brain Mapping
Issue number11
Publication statusPublished - Nov 2009
Externally publishedYes


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