PT  - JOURNAL ARTICLE
AU  - Fan Zhang
AU  - Anna Breger
AU  - Kang Ik Kevin Cho
AU  - Lipeng Ning
AU  - Carl-Fredrik Westin
AU  - Lauren J. O’Donnell
AU  - Ofer Pasternak
TI  - Deep Learning Based Segmentation of Brain Tissue from Diffusion MRI
AID  - 10.1101/2020.07.30.228809
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.07.30.228809
4099  - http://biorxiv.org/content/early/2020/07/31/2020.07.30.228809.short
4100  - http://biorxiv.org/content/early/2020/07/31/2020.07.30.228809.full
AB  - Segmentation of brain tissue types from diffusion MRI (dMRI) is an important task, required for quantification of brain microstructure and for improving tractography. Current dMRI segmentation is mostly based on anatomical MRI (e.g., T1- and T2-weighted) segmentation that is registered to the dMRI space. However, such inter-modality registration is challenging due to more image distortions and lower image resolution in the dMRI data as compared with the anatomical MRI data. In this study, we present a deep learning method that learns tissue segmentation from high-quality imaging datasets from the Human Connectome Project (HCP), where registration of anatomical data to dMRI is more precise. The method is then able to predict a tissue segmentation directly from new dMRI data, including data collected with a different acquisition protocol, without requiring anatomical data and inter-modality registration. We train a convolutional neural network (CNN) to learn a tissue segmentation model using a novel augmented target loss function designed to improve accuracy in regions of tissue boundary. To further improve accuracy, our method adds diffusion kurtosis imaging (DKI) parameters that characterize non-Gaussian water molecule diffusion to the conventional diffusion tensor imaging parameters. The DKI parameters are calculated from the recently proposed mean-kurtosis-curve method that corrects implausible DKI parameter values and provides additional features that discriminate between tissue types. We demonstrate high tissue segmentation accuracy on HCP data, and also when applying the HCP-trained model on dMRI data from a clinical acquisition with lower resolution and fewer gradient directions.Competing Interest StatementThe authors have declared no competing interest.