Daniele Perrone

Isotropic non-white matter partial volume effects in constrained spherical deconvolution.

Diffusion-weighted (DW) magnetic resonance imaging (MRI) is a non-invasive imaging method, which can be used to investigate neural tracts in the white matter (WM) of the brain. Significant partial volume effects (PVEs) are present in the DW signal due to relatively large voxel sizes. These PVEs can be caused by both non-WM tissue, such as gray matter (GM) and cerebrospinal fluid (CSF), and by multiple non-parallel WM fiber populations. High angular resolution diffusion imaging (HARDI) methods have been developed to correctly characterize complex WM fiber configurations, but to date, many of the HARDI methods do not account for non-WM PVEs. In this work, we investigated the isotropic PVEs caused by non-WM tissue in WM voxels on fiber orientations extracted with constrained spherical deconvolution (CSD). Experiments were performed on simulated and real DW-MRI data. In particular, simulations were performed to demonstrate the effects of varying the diffusion weightings, signal-to-noise ratios (SNRs), fiber configurations, and tissue fractions. Our results show that the presence of non-WM tissue signal causes a decrease in the precision of the detected fiber orientations and an increase in the detection of false peaks in CSD. We estimated 35–50% of WM voxels to be affected by non-WM PVEs. For HARDI sequences, which typically have a relatively high degree of diffusion weighting, these adverse effects are most pronounced in voxels with GM PVEs. The non-WM PVEs become severe with 50% GM volume for maximum spherical harmonics orders of 8 and below, and already with 25% GM volume for higher orders. In addition, a low diffusion weighting or SNR increases the effects. The non-WM PVEs may cause problems in connectomics, where reliable fiber tracking at the WM–GM interface is especially important. We suggest acquiring data with high diffusion-weighting 2500–3000 s/mm2, reasonable SNR (~30) and using lower SH orders in GM contaminated regions to minimize the non-WM PVEs in CSD.

The effect of Gibbs ringing artifacts on measures derived from diffusion MRI.

Diffusion-weighted (DW) magnetic resonance imaging (MRI) is a unique method to investigate microstructural tissue properties noninvasively and is one of the most popular methods for studying the brain white matter in vivo. To obtain reliable statistical inferences with diffusion MRI, however, there are still many challenges, such as acquiring high-quality DW-MRI data (e.g., high SNR and high resolution), careful data preprocessing (e.g., correcting for subject motion and eddy current induced geometric distortions), choosing the appropriate diffusion approach (e.g., diffusion tensor imaging (DTI), diffusion kurtosis imaging (DKI), or diffusion spectrum MRI), and applying a robust analysis strategy (e.g., tractography based or voxel based analysis). Notwithstanding the numerous efforts to optimize many steps in this complex and lengthy diffusion analysis pipeline, to date, a well-known artifact in MRI--i.e., Gibbs ringing (GR)--has largely gone unnoticed or deemed insignificant as a potential confound in quantitative DW-MRI analysis. Considering the recent explosion of diffusion MRI applications in biomedical and clinical applications, a systematic and comprehensive investigation is necessary to understand the influence of GR on the estimation of diffusion measures. In this work, we demonstrate with simulations and experimental DW-MRI data that diffusion estimates are significantly affected by GR artifacts and we show that an off-the-shelf GR correction procedure based on total variation already can alleviate this issue substantially.

Informed constrained spherical deconvolution (iCSD)

Diffusion-weighted (DW) magnetic resonance imaging (MRI) is a noninvasive imaging method, which can be used to investigate neural tracts in the white matter (WM) of the brain. However, the voxel sizes used in DW-MRI are relatively large, making DW-MRI prone to significant partial volume effects (PVE). These PVEs can be caused both by complex (e.g. crossing) WM fiber configurations and non-WM tissue, such as gray matter (GM) and cerebrospinal fluid. High angular resolution diffusion imaging methods have been developed to correctly characterize complex WM fiber configurations, but significant non-WM PVEs are also present in a large proportion of WM voxels. In constrained spherical deconvolution (CSD), the full fiber orientation distribution function (fODF) is deconvolved from clinically feasible DW data using a response function (RF) representing the signal of a single coherently oriented population of fibers. Non-WM PVEs cause a loss of precision in the detected fiber orientations and an emergence of false peaks in CSD, more prominently in voxels with GM PVEs. We propose a method, informed CSD (iCSD), to improve the estimation of fODFs under non-WM PVEs by modifying the RF to account for non-WM PVEs locally. In practice, the RF is modified based on tissue fractions estimated from high-resolution anatomical data. Results from simulation and in-vivo bootstrapping experiments demonstrate a significant improvement in the precision of the identified fiber orientations and in the number of false peaks detected under GM PVEs. Probabilistic whole brain tractography shows fiber density is increased in the major WM tracts and decreased in subcortical GM regions. The iCSD method significantly improves the fiber orientation estimation at the WM-GM interface, which is especially important in connectomics, where the connectivity between GM regions is analyzed.

Reproducibility and intercorrelation of graph theoretical measures in structural brain connectivity networks

HighlightsReproducibility of CSD‐based structural brain connectomics is generally excellent.A minimum of one million streamlines are required for excellent reproducibility.Reproducibility continues to increase further for higher numbers of streamlines.Thresholds in the reconstruction of binary networks should be sufficiently high.Higher order models decrease the reproducibility, but only slightly. ABSTRACT Diffusion‐weighted magnetic resonance imaging can be used to non‐invasively probe the brain microstructure. In addition, recent advances have enabled the identification of complex fiber configurations present in most of the white matter. This has improved the investigation of structural connectivity with tractography methods. Whole‐brain structural connectivity networks, or connectomes, are reconstructed by parcellating the gray matter and performing tractography to determine connectivity between these regions. These complex networks can be analyzed with graph theoretical methods, which measure their global and local properties. However, as these tools have only recently been applied to structural brain networks, there is little information about the reproducibility and intercorrelation of network properties, connectivity weights and fiber tractography reconstruction parameters in the brain. We studied the reproducibility and correlation in structural brain connectivity networks reconstructed with constrained spherical deconvolution based probabilistic streamlines tractography. Diffusion‐weighted data from 19 subjects were acquired with b = 2800 s/mm2 and 75 gradient orientations. Intrasubject variability was computed with residual bootstrapping. Our findings indicate that the reproducibility of graph theoretical metrics is generally excellent with the exception of betweenness centrality. A reconstruction density of approximately one million streamlines is necessary for excellent reproducibility, but the reproducibility increases further with higher densities. The reproducibility decreases, but only slightly, when switching to a higher order in constrained spherical deconvolution. Moreover, in binary networks, using sufficiently high threshold values improves the reproducibility. We show that multiple network properties and connectivity weights are highly intercorrelated. The experiments were replicated by using a test‐retest dataset of 44 healthy subjects provided by the Human Connectome Project. In conclusion, our results provide guidelines for reproducible investigation of structural brain networks. Graphical abstract Figure. No caption available.