TY - JOUR
T1 - Tensor-based morphometry using scalar and directional information of diffusion tensor MRI data (DTBM)
T2 - Application to hereditary spastic paraplegia
AU - Sadeghi, Neda
AU - Arrigoni, Filippo
AU - D'Angelo, Maria Grazia
AU - Thomas, Cibu
AU - Irfanoglu, M. Okan
AU - Hutchinson, Elizabeth B.
AU - Nayak, Amritha
AU - Modi, Pooja
AU - Bassi, Maria Teresa
AU - Pierpaoli, Carlo
N1 - Funding Information:
This research was supported by the Intramural Research Program of the NIH, including the National Institute of Biomedical Imaging and Bioengineering (NIBIB) and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). Support for this work included funding from the U01 HD079068-01 grant, the Department of Defense in the Center for Neuroscience and Regenerative Medicine (CNRM) (HJF Award#: 30613610.0160855), and Congressionally Directed Medical Research Programs (CDMRP) (HJF Award#: W81XWH-13-2-0019). Authors thank Dr. Henry Eden for his assistance with editing this manuscript.
Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2018/12
Y1 - 2018/12
N2 - Tensor-based morphometry (TBM) performed using T1-weighted images (T1WIs) is a well-established method for analyzing local morphological changes occurring in the brain due to normal aging and disease. However, in white matter regions that appear homogeneous on T1WIs, T1W-TBM may be inadequate for detecting changes that affect specific pathways. In these regions, diffusion tensor MRI (DTI) can identify white matter pathways on the basis of their different anisotropy and orientation. In this study, we propose performing TBM using deformation fields constructed using all scalar and directional information provided by the diffusion tensor (DTBM) with the goal of increasing sensitivity in detecting morphological abnormalities of specific white matter pathways. Previously, mostly fractional anisotropy (FA) has been used to drive registration in diffusion MRI-based TBM (FA-TBM). However, FA does not have the directional information that the tensors contain, therefore, the registration based on tensors provides better alignment of brain structures and better localization of volume change. We compare our DTBM method to both T1W-TBM and FA-TBM in investigating differences in brain morphology between patients with complicated hereditary spastic paraplegia of type 11 (SPG11) and a group of healthy controls. Effect size maps of T1W-TBM of SPG11 patients showed diffuse atrophy of white matter. However, DTBM indicated that atrophy was more localized, predominantly affecting several long-range pathways. The results of our study suggest that DTBM could be a powerful tool for detecting morphological changes of specific white matter pathways in normal brain development and aging, as well as in degenerative disorders.
AB - Tensor-based morphometry (TBM) performed using T1-weighted images (T1WIs) is a well-established method for analyzing local morphological changes occurring in the brain due to normal aging and disease. However, in white matter regions that appear homogeneous on T1WIs, T1W-TBM may be inadequate for detecting changes that affect specific pathways. In these regions, diffusion tensor MRI (DTI) can identify white matter pathways on the basis of their different anisotropy and orientation. In this study, we propose performing TBM using deformation fields constructed using all scalar and directional information provided by the diffusion tensor (DTBM) with the goal of increasing sensitivity in detecting morphological abnormalities of specific white matter pathways. Previously, mostly fractional anisotropy (FA) has been used to drive registration in diffusion MRI-based TBM (FA-TBM). However, FA does not have the directional information that the tensors contain, therefore, the registration based on tensors provides better alignment of brain structures and better localization of volume change. We compare our DTBM method to both T1W-TBM and FA-TBM in investigating differences in brain morphology between patients with complicated hereditary spastic paraplegia of type 11 (SPG11) and a group of healthy controls. Effect size maps of T1W-TBM of SPG11 patients showed diffuse atrophy of white matter. However, DTBM indicated that atrophy was more localized, predominantly affecting several long-range pathways. The results of our study suggest that DTBM could be a powerful tool for detecting morphological changes of specific white matter pathways in normal brain development and aging, as well as in degenerative disorders.
KW - DTBM
KW - deformation-based morphometry
KW - diffusion
KW - diffusion tensor MRI
KW - diffusion tensor imaging
KW - hereditary spastic paraplegia
KW - spastic paraplegia of type 11
KW - tensor-based morphometry
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U2 - 10.1002/hbm.24278
DO - 10.1002/hbm.24278
M3 - Article
C2 - 30253021
AN - SCOPUS:85053780358
SN - 1065-9471
VL - 39
SP - 4643
EP - 4651
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 12
ER -