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Sarah A. Morrow

Publications and source records attributed to Sarah A. Morrow.

2 recordsLinked to original sources

Longitudinal tracking of multiple sclerosis lesions in the spinal cord: A validation study

Longitudinal characterization of multiple sclerosis (MS) lesions remains constrained by the lack of frameworks capable of establishing consistent instance-level correspondences across time. Conventional segmentation approaches produce semantic lesion masks at each visit and therefore fail to capture the complex instance temporal patterns associated with lesion appearance, disappearance, splitting, or merging. This study presents a comparative evaluation of five strategies for automated tracking of spinal cord MS lesions in longitudinal MRI data from a multi-site cohort. The investigated strategies rely either on deformable registration or on a spinal anatomical reference system, and encompass overlap-based matching, coordinate-based Hungarian algorithm, gradient-boosted classification, and Siamese model classification. Tracking accuracy is quantified using instance-level true positives, false positives, and false negatives, allowing to assess the presence of one-to-many and many-to-one associations. Results show best performance for the registration-based overlap method. This study provides the first systematic analysis of lesion-instance correspondence in the spinal cord and outlines the strengths and limitations of registration-based and registration-free paradigms for longitudinal MS assessment. The code is available at http://github.com/ivadomed/longitudinal-sc-ms-lesion-tracking .

cs.CV↗

Lesion-Independent Associations Between Thalamic Nuclei Volumes and Information Processing Speed in Multiple Sclerosis

Background: Cognitive impairment in multiple sclerosis (MS) is driven by both focal inflammation and compartmentalized neurodegeneration, yet the relative effect of lesion-independent thalamic atrophy on information processing speed (IPS) remains unclear. Methods: This retrospective cohort study included 100 participants with MS. Automatic segmentation techniques quantified lesion load and delineated 26 thalamic regions of interest (ROIs). Linear models compared associations between ROI volumes and Symbol Digit Modalities Test (SDMT) performance in lesion-adjusted and unadjusted models. Results: Twenty-one of 26 ROIs showed significant SDMT associations before lesion adjustment; twelve remained significant after adjustment. Lesion-independent associations were observed in the global thalamus, sensory relay nuclei (ventral posterolateral, medial and lateral geniculate), and associative hubs (pulvinar and mediodorsal-parafascicular complex). These processing-associated ROIs exhibited significantly lower lesion-mediated effects (13.4%) than those losing significance after adjustment (34.2%, p < 0.001). Conclusion: Our findings suggest that IPS impairment reflects heterogeneous contributions from focal lesion-driven and chronic neurodegenerative pathology, with nucleus-specific phenotyping potentially informing identification of higher risk individuals.

q-bio.NC↗