Cognitive profiles associated with faster thalamic atrophy in multiple sclerosis.
Authors
Affiliations (4)
Affiliations (4)
- Mellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, United States. Electronic address: [email protected].
- John Carroll University, OH, USA.
- Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, United States.
- Mellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, United States.
Abstract
Cognitive impairment (CI) in people with MS (pwMS) has complex pathophysiology. Neuropsychological testing (NPT) can be helpful, but interpretation may be challenging for clinicians. Thalamic atrophy (TA) has shown correlation for both neurodegeneration and CI. Leverage machine learning methods to link CI and longitudinal neuroimaging biomarkers. Retrospective review of adult pwMS with NPT and ≥2 brain MRIs. Quantitative MRI regional change rates were calculated using mixed effects models. Participants were divided into training and validation cohorts. K-means clustering was done based on first and second NPT principal components (PC1 and PC2). MRI change rates were compared between clusters. 112 participants were included (mean age 48 years, 71 % female, 80 % relapsing remitting). Processing speed and memory were the major contributors to PC1. We identified two clusters based on PC1, one with significantly more TA in both training and validation cohorts (p = 0.035; p = 0.002) and similar rates of change in all other quantitative MRI measures. The most important contributors to PC1 included measures of processing speed (SDMT/WAIS Coding) and memory (List Learning/BVMT immediate and delayed recall). This clustering method identified a profile of NPT results strongly linked to and possibly driven by TA. These results confirm validity of previously established findings using more advanced analyses in addition to offering novel insights into NPT dimensionality reduction.