Multi-tissue constrained spherical deconvolution¶
Introduction¶
Multi-tissue constrained spherical deconvolution (CSD) of multi-shell data exploits the unique b-value dependencies of the different macroscopic tissue types (WM/GM/CSF) to estimate a multi-tissue orientation distribution function (ODF) as explained in Jeurissen et al. (2014). As it includes separate compartments for each tissue type, it can produce a map of the WM/GM/CSF signal contributions directly from the DW data. In addition, the more complete modelling of the DW signal results in more accurate apparent fiber density (AFD) measures and more precise fibre orientation estimates at the tissue interfaces.
User guide¶
Multi-tissue CSD can be performed as:
dwi2fod msmt_csd dwi.mif wm.txt wm.mif gm.txt gm.mif csf.txt csf.mif
where
dwi.mifis the dwi data set (input)<tissue>.txtis the tissue-specific response function (input)<tissue>.mifis the tissue-specific ODF (output)
Note that input response functions and their corresponding output ODFs need to be specified in pairs.
Typically, you will also want to use the -mask to avoid calculations in non-brain voxels:
dwi2fod msmt_csd -mask mask.mif dwi.mif wm.txt wm.mif gm.txt gm.mif csf.txt csf.mif
RGB tissue signal contribution maps can be obtained as follows:
mrconvert -coord 3 0 wm.mif - | mrcat csf.mif gm.mif - vf.mif
The resulting WM fODFs can be displayed together with the tissue signal contribution map as:
mrview vf.mif -odf.load_sh wm.mif
Per tissue response function estimation¶
Input response functions for CSF, GM and single fibre WM can be estimated from the data using prior tissue segmentations, similarly to that described in Jeurissen et al. (2014) using the dwi2response msmt_5tt command:
dwi2response msmt_5tt dwi.mif 5tt.mif wm.txt gm.txt csf.txt
where
dwi.mifis the same dwi data set as used above (input)5tt.mifis a tissue type segmentation of a coregistered T1 data set from the same subject (input)<tissue>.txtis the tissue-specific response function as used above (output)
Prior tissue type segmentation can be obtained from a structural T1 scan using the 5ttgen script:
5ttgen fsl T1.mif 5tt.mif
where
T1.mifis a coregistered T1 data set from the same subject (input)5tt.mifis the tissue type segmentation used above (output)
The difference between the default behaviour of dwi2response msmt_5tt and the method described in Jeurissen et al. (2014) is that instead of selecting WM single-fibre voxels using an FA threshold, the dwi2response tournier algorithm is instead used.
Note that this process is dependent on accurate correction of EPI geometric distortions, and rigid-body registration between the DWI and T1 modalities, such that the T1 image can be reliably used to select pure-tissue voxels in the DWI volumes. Failure to achieve these may result in inappropriate voxels being used for response function estimation, with concomitant errors in tissue estimates.