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Cortical projections of the superoanterior fasciculus (SAF)
Szabolcs David1, Michel Thiebaut de Schotten2, Fenghua Guo1, Flavio Dell’Acqua3, Alexander Leemans1, and Alberto de Luca1
1Image Sciences Institute, UMC Utrecht, Utrecht, Netherlands, 2Brain Connectivity and Behaviour Laboratory, Sorbonne Universities, Paris, France, 3NatBrainLab, Department of Forensics and Neurodevelopmental Sciences, Sackler Institute for Translational Neurodevelopment, King's College London, London, United Kingdom

Synopsis

The superoanterior fasciculus (SAF) is defined as a bilateral tract in the frontal lobe that resembles the structure of the anterior cingulum, but is located superior, anterior and lateral. In this work, we investigated the cortical projections of the structure utilizing the latest multi-shell multi tissue (MSMT) constrained spherical deconvolution (CSD) method to analyze diffusion MRI data from the Human Connectome Project (HCP). Our results show that the paracentral lobular, mid cingulate cortex and the orbital- and polar frontal cortex show high SAF termination prevalence, suggesting a novel connection in the frontal lobe.

Introduction

The superoanterior fasciculus (SAF) is defined as a bilateral tract in the frontal lobe that resembles the structure of the anterior cingulum, but is located superior, anterior and lateral. It was first identified in a recent investigation [1] using diffusion MRI (dMRI) with support from dissection [2] and polarized light imaging (PLI) [3]. The pathway appears to spread from the rostrum of the corpus callosum (CC) to the ascending ramus of the cingulate sulcus and is medial to the corona radiate. While the first investigation revealed the existence and discussed the prevalence of the SAF, the functional assessment of the structure remains uncharted. Cortical projection of fiber bundles offer insight into the functional involvement of a tract with comparing functional MRI (fMRI) [4], cytoarchitecture [5] or multimodal imaging [6] derived population-based maps. Previously, disconnectome studies [7] demonstrated the utility of the method in neuroscience [8], [9] as well as clinical studies [10], [11]. In this work, we explored the cortical projections of the SAF.

Methods

Minimally pre-processed dMRI data were collected from the S500 release of the Human Connectome Project (HCP) [12], [13]. Briefly, a motion- and distortion corrected dataset consists 18 non-DWIs (b-value = 0 s/mm2) and 90 DWIs per shell with b-values equal to 1000/2000/3000 s/mm2, with a voxel size of 1.25mm isotropic and a sample size of 89 participants. Fiber orientation distribution (FOD) estimation was performed with the Generalized Richardson-Lucy (GRL) [14] method, which distinctly models the response functions (RF) of white matter (WM), grey matter (GM) and cerebrospinal fluid (CSF). The RF of WM was defined using the diffusion tensor imaging (DTI)-based fixed tensor modelling using all 288 DWI volumes. In addition, we also corrected for the gradient nonlinearities in the diffusion-weighted gradients during the FOD estimation procedure [15]–[17]. Then deterministic fiber tractography (FT) was performed in ExploreDTI [18] using spherical-harmonics of order 16. For tracking the SAF, automated tract selection was obtained by atlas-based tractography segmentation [19]. On the template dataset, we defined 4 Boolean ‘AND’ and ‘NOT’ ROIs: 2 axial AND, 1 sagittal NOT and 1 coronal NOT ROIs. The 2 axial AND ROIs were placed as follows: the first one was located at the height of approximately half the genu of the corpus callosum (CC) and the second ROI was placed 10 slices superior. A NOT ROI was placed midsagittal to exclude fiber pathways from the corpus callosum (CC) and one NOT was placed coronal posterior the genu below and above CC to exclude fibers from the inferior fronto-occipital fasciculus (iFOF) and the cingulum. After tracking the SAF, the binarized mask of the tract termination-points were transformed to MNI space, using the warp-files provided by the HCP-team, then mapped to the Freesurfer [20] surface template via the computational anatomy toolbox (CAT) [21]. Mean prevalence of tract terminations per vertex are presented on the inflated- and the central surfaces.

Results

Fig. 1 shows the location of the SAF in the HCP example subject. Fig. 2 shows the prevalence overview of the SAF in MNI space from 89 subjects. Fig. 3 shows the surface projected overview of the SAF. Fig. 4 shows the table of prevalence of the SAF based on the Desikan-Killiany [22], the Destrieux [23] and the HCP Multimodal [6] surface atlases. Clearly, the SAF shows coherent patterns in structural connectivity with high termination prevalence in the paracentral lobular, mid cingulate cortex as well as in the orbital- and polar frontal cortex.

Discussion and Conclusion

In this work, we investigated the cortical connections of a recently proposed new fiber bundle, the superoanterior fasciculus. The SAF was revealed with the combination of large scale, high quality imaging data and the advanced dMRI models, capable of disentangling multiple fiber populations in a single voxel. The current nomenclature classifies the SAF as part of the large dorsal system of horizontal fibers connecting frontal and parietal cortices as a branch of the mesial longitudinal system (MesLS) [24]. While the SAF has not been reproduced neither with dissection nor with imaging studies so far, present investigation proposes a novel connection in the frontal lobe. The short-term or U-fiber connections have been described before [25] and long-term connections are well-known from primate [26] and human [27] studies, the frontal lobe remains a challenging region to study due to extensive geometrical distortions caused by the air-tissue interface of the sinuses.

Acknowledgements

No acknowledgement found.

References

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Figures

Fig. 1 Location of the superoanterior fasciculus in the right hemisphere (SAF) is shown for the example subject of the Human Connectome Project (HCP), with the associated T1w image as the background, which was further enhanced with the local dominant direction of diffusion. The color-encoding corresponds to left-right in red, front-back green and up-down orientations in blue. The sagittal plane is located 10 slices (or 12.5mm) to the right from the midsagittal plane.

Fig. 2 Volumetric overview is shown for the superoanterior fasciculus (SAF) tract terminations in MNI space. Percentage (%) indicates the fraction of subjects for which the tract is terminated in a given voxel for the SAF. The distance between slices is 5mm for the sagittal (with a 10 mm gap in the midline) and coronal views, while it is 8mm for the axial view.

Fig. 3 Surface overview is shown for the superoanterior fasciculus (SAF) tract terminations on the surface average template via Freesurfer. Percentage (%) indicates the fraction of subjects for which the tract is terminated in a given vertex for the SAF. The inflated surfaces are shown in the corners, highlighting some of the highest SAF prevalence areas from the HCP Multimodal atlas, while in the middle the SAF distribution on the central surface is shown anterior.

Fig. 4 shows the table of mean percentage (%) prevalence of the superoanterior fasciculus (SAF) based on the Desikan Killiany, the Destrieux and the HCP Multimodal surface atlases.

Proc. Intl. Soc. Mag. Reson. Med. 28 (2020)
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