Corticospinal Tract (CST) reconstruction based on fiber orientation distributions(FODs) tractography
Youshan Zhang

TL;DR
This paper presents a novel method for reconstructing the corticospinal tract (CST) using fiber orientation distributions (FODs) tractography, which improves anatomical accuracy over traditional tensor-based methods, aiding spinal cord injury treatment.
Contribution
The study introduces FODs tractography for CST reconstruction, utilizing spherical harmonics and manual ROI delineation to enhance anatomical detail compared to tensor-based approaches.
Findings
FODs tractography reveals more accurate CST fiber bundles.
The method outperforms tensor-based tractography in anatomical correctness.
Manual ROI delineation effectively supports CST reconstruction.
Abstract
The Corticospinal Tract (CST) is a part of pyramidal tract (PT), and it can innervate the voluntary movement of skeletal muscle through spinal interneurons (the 4th layer of the Rexed gray board layers), and anterior horn motorneurons (which control trunk and proximal limb muscles). Spinal cord injury (SCI) is a highly disabling disease often caused by traffic accidents. The recovery of CST and the functional reconstruction of spinal anterior horn motor neurons play an essential role in the treatment of SCI. However, the localization and reconstruction of CST are still challenging issues; the accuracy of the geometric reconstruction can directly affect the results of the surgery. The main contribution of this paper is the reconstruction of the CST based on the fiber orientation distributions (FODs) tractography. Differing from tensor-based tractography in which the primary direction is…
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Taxonomy
TopicsAdvanced Neuroimaging Techniques and Applications · Cerebral Palsy and Movement Disorders · Spinal Dysraphism and Malformations
Corticospinal Tract (CST) reconstruction based on fiber orientation distributions (FODs) tractography
Authors Name/s per 1st Affiliation (Author)
line 1 (of Affiliation): dept. name of organization
line 2: name of organization, acronyms acceptable
line 3: City, Country
line 4: Email: [email protected]
Youshan Zhang
Computer Science and Engineering Department
Lehigh University
Bethlehem, PA
Abstract
The Corticospinal Tract (CST) is a part of pyramidal tract (PT) and it can innervate the voluntary movement of skeletal muscle through spinal interneurons (the 4th layer of the Rexed gray board layers), and anterior horn motorneurons (which control trunk and proximal limb muscles). Spinal cord injury (SCI) is a highly disabling disease often caused by traffic accidents. The recovery of CST and the functional reconstruction of spinal anterior horn motor neurons play an essential role in the treatment of SCI. However, the localization and reconstruction of CST are still challenging issues, the accuracy of the geometric reconstruction can directly affect the results of the surgery. The main contribution of this paper is the reconstruction of the CST based on the fiber orientation distributions (FODs) tractography. Differing from tensor-based tractography in which the primary direction is a determined orientation, the direction of FODs tractography is determined by the probability. The spherical harmonics (SPHARM) can be used to approximate the efficiency of FODs tractography. We manually delineate the three ROIs (the posterior limb of the internal capsule, the cerebral peduncle, and the anterior pontine area) by the ITK-SNAP software, and use the pipeline software to reconstruct both the left and right sides of the CST fibers. Our results demonstrate that FOD-based tractography can show more and correct anatomical CST fiber bundles.
Index Terms:
Corticospinal Tract reconstruction; fiber orientation distributions; tractography;
I Introduction
The Corticospinal Tract (CST) is a part of pyramidal tract (PT), and many of its fibers originate from the primary motor cortex (the precentral gyrus) then terminate in the spinal cord [1, 2]. The CST is thought to originate from the premotor area, the supplementary motor area, and the somatosensory cortex, and then terminate at the thoracic levels (20%), lumbosacral levels (25%) and cervical levels (55%) [3, 4]. Evidence shows that the CST serves as the major downstream motor tract in the mammalian spinal cord, and the fibers control the voluntary movement of skeletal muscle by directly or indirectly innervating the neurons in the anterior horn [5]. However, the structural and functional properties of the CST are far more complex than researchers previously thought, and we continue to have a new understanding about the CST with the advancement of technology, thus the CST is still one of the hotspots in neuroscience research [6, 7, 8]. About 75%-90% of the CST fibers descend to the lateral corticospinal tract by decussation of the pyramid, but a few fibers form the anterior corticospinal tract by not crossing the pyramid [9, 10]. The fibers, which first passed through the medial posterior spinocerebellar tract then went into the lumbosacral spinocerebellar tract, were not yet appeared [11, 12]. The main function of the CST is innervating the voluntary movement of skeletal muscle through spinal interneurons (the 4th layer of the Rexed gray board layers), and anterior horn motorneurons (which control trunk and proximal limb muscles), then the CST terminates in the spinal motor cells (which control the fine motor of small muscle in extremities) [13]. Spinal cord injury (SCI) is a highly disabling disease in clinical practice. With the popularization of modern transport vehicles and the acceleration of the process of industrialization, the number of patients with SCI is increasing day by day, many people were injured in traffic accidents. If the CST is damaged, it can seriously affect the quality of life of patients and even lead to paralysis. Patients with rigid muscle, spasm, paralysis and other pathologies are usually considered to have CST injury [14]. When the CST is damaged in the SCI, the motor pathways are affected, and these surviving spinal cord nerve cells, which are below the injury surface, lose neural innervation of the brain, and are unable to perform the random functional activity [15]. In addition, the repair of the CST after the SCI is still a vital research topic in neuroscience, and the recovery of limb motor function can be promoted by the CST repair or functional remodeling. Although many types of experimental research have made great progress, there has been no report of successful clinical application [16]. Therefore, the recovery of CST and the functional reconstruction of spinal anterior horn motor neurons play an essential role in the treatment of SCI [17]. However, the localization and reconstruction of CST are still challenging issues, and the accuracy of the geometric reconstruction can directly affect the results of the surgery. Furthermore, there are few methods that can be used to reconstruct the CST and the validation of clinical application is still uncertain [18].
Diffusion tensor imaging (DTI) is a non-invasive technique that can estimate the integrity of the white matter tracts by using the diffusion of water molecules [19, 20, 21]. Diffusion tensor tractography (DTT), a three-dimensional visualized version of DTI, has been widely used to reconstruct the CST [8, 22, 23]. However, there are several challenges in these papers. Firstly, the seed regions or the regions of interest (ROIs) are different in these papers, the models of these papers did not cover all the anatomic areas of the CST, and the results did not reflect the complexity of the CST fibers. Secondly, the validation of these models in the clinical application still not fully clarified.
The main contribution of this paper is the reconstruction of the CST based on the fiber orientation distributions (FODs) tractography [24, 25]. The major difference between the FODs tractography and the tensor-based tractography is the definition of the tracts direction. Tensor-based tractography relies on the three non-negative eigenvalues and eigenvectors, the main direction is a determined orientation [26]. The FOD tractography is fiber orientation distribution (the direction is determined by the probability), the spherical harmonics (SPHARM) can be used to approximate the efficiency of FOD [24]. In this paper, we manually delineate the ROIs by the ITK-SNAP software[27], and use the Lab of NeuroImaging (LONI) pipeline software[28] to reconstruct both the left and right sides of the CST fibers. Our results demonstrate that FOD-based tractography can show correct anatomical CST fiber bundles.
II Method
II-A Data
In this paper, the data are from Human Connectome Project (HCP) [29], which can be found on LONI IDA (https://ida.loni.usc.edu/services/NewUser.jsp) or ConnectomeDB (https://db.humanconnectome.org/app/template/Login.vm) . Figure 1 shows the four images ( fiber orientation distributions (FOD), fractional anisotropy(FA), CortexLabel and Mask), which are used to reconstruct the CST fibers.
II-B ROIs
The CST primarily originates from the motor cortex (the precentral gyrus), then descends to the forebrain, pons, medulla, and pyramidal decussation and terminates at thoracic levels, lumbosacral levels, and cervical levels. Therefore, the ROIs should be in these different areas, but the proper ROIs are still hard to decide. Many papers used the precentral gyrus as the starting point since precentral gyrus is the major area controls the movement of the arm, leg and the trunk [30, 8, 31]. However, the organization of the fibers can be distorted in patients with brain tumors [8], so more ROIs along the CST should be included. Another two ROIs (the posterior limb of the internal capsule (PLIC) and anterior pontine area (aiP)) were used in Carolin et al., 2015. The internal capsule lies in the forebrain, the pons is a part of the brainstem, both of these two regions are involved in the movement pathways, they can affect the movement of the leg, trunk, and arm. Therefore, the PLIC and aiP are two essential ROIs. Several papers showed that the cerebral peduncle (CP) of the midbrain is another important ROI of the CST reconstruction, since it also involved in innervating the movement pathways [30, 32]. Although Venkateswaran and Erik, 2017 used centrum semiovale at top of lateral ventricle (CSoLV) as additional ROIs[6], the CSoLV is not significant comparing with the other three ROIs, therefore, we exclude this area in our study. In this paper, the seed region is the precentral gyrus, the ROIs are the PLIC, CP and the aiP. Figure 2 shows the seed region and ROIs in the CST reconstruction.
II-C Workflow of the Pipeline
We use Pipeline software [28] to reconstruct the CST fibers after we choose the seed region and the ROIs. Figure 3 shows the reverent workflow of the Pipeline when we compute the fibers of the CST.
II-D Parameters
The input files Mask, FOD, and CortexLabel are the three images which are mentioned in section A (data part), the CST_ROIs are the images which are generated by manual delineation by the ITK-SNAP. The number of the tracks set as 1000, the radius is the 1.5, the cortex label of left precentral gyrus is 49 and the right precentral gyrus is 50. Besides, the left labels of the three ROIs are 1, 3 and 5, and the right labels are the 2, 4, and 6. The left and the right CST fibers are computed separately, the cortex label and the ROIs labels should be consistent with the above parameters.
II-E Outlier tracts remove
The result of the workflow is a tck file, we convert it into the trk file by Matlab since the BrainSuite software [33] cannot recognize the tck files. In addition, some fibers are not normal and may be too long and project to other areas. Firstly, we filter the outlier tracts, and then some obvious abnormal tracts are removed using the BrainSuite 16 a1 track filtering options.
III Results
The reconstructed CST fibers are visualized by the BrainSuite 16 a1, to show the anatomical validity of the reconstruction results, we overlay the CST fiber bundles with the FA image. Fig. 4 and 5 show the projection to the precentral gyrus by overlaying the fiber tracts with the cortex label and FA images. Fig. 6 shows the results of the CST fibers through the posterior of the internal capsule and the thalamus. Fig. 7 shows the results of the cerebral peduncle by overlaying the fiber bundles with the FA image. And the Fig. 8 overlays the fiber bundle with the FA image to the anterior pontine area. These results demonstrate that the fiber bundles are anatomically correct. Furthermore, these results prove that the FOD-based tractography can provide a smooth, clear and reliable reconstruction of the CST fibers.
IV Discussion
Comparing our results with [34, 35], our reconstruction results show more fibers, which shows the high accuracy of our methods. One limitation of the paper is that we only choose three ROIs (the posterior limb of the internal capsule, the cerebral peduncle, and the anterior pontine area); there are more regions which can be explored, such as top of the lateral ventricle (CSoLV) though it might not be as important as above three ROIs, it still can be an interesting direction. Our study also had a limited sample size. However, Our tractography findings suggest the FODs reconstruction method can accurately reconstruct the CST fibers; thus, the power of our study is sufficient. For future work, we should explore our reconstruction of the CST in recovery from the SCI injury.
V Conclusion
In this paper, we reconstruct the Corticospinal Tract using fiber orientation distributions tractography. Comparing with determined orientation tensor-based tractography, the main direction of FODs is based on probabilistic direction. We manually delineate the three ROIs (the posterior limb of the internal capsule, the cerebral peduncle, and the anterior pontine area) by the ITK-SNAP software and use the pipeline software reconstructs both the left and right sides of the CST fibers. Our results demonstrate that FOD-based tractography can show correct anatomical CST fiber bundles. The results of our study show that the accurate reconstruction of CST can be applied in improving both diagnostics and treatment of Spinal cord injury in the future.
Acknowledgment
We want to thank professor Yonggang Shi for guiding us to do research on this topic and give us valuable suggestions in explaining the topic more professionally.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
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