Abstract

Background: Cortical and thalamic pathologies have been associated with cognitive impairment in patients with multiple sclerosis (MS).Objective: We aimed to quantify cortical and thalamic damage in patients with MS using a high-resolution T1 mapping technique and to evaluate the association of these changes with clinical and cognitive impairment.Methods: The study group consisted of 49 patients with mainly relapsing-remitting MS and 17 age-matched healthy controls who received 3T MRIs including a T1 mapping sequence (MP2RAGE). Mean T1 relaxation times (T1-RT) in the cortex and thalami were compared between patients with MS and healthy controls. Additionally, correlation analysis was performed to assess the relationship between MRI parameters and clinical and cognitive disability.Results: Patients with MS had significantly decreased normalized brain, gray matter, and white matter volumes, as well as increased T1-RT in the normal-appearing white matter, compared to healthy controls (p < 0.001). Partial correlation analysis with age, sex, and disease duration as covariates revealed correlations for T1-RT in the cortex (r = −0.33, p < 0.05), and thalami (right thalamus: r = −0.37, left thalamus: r = −0.50, both p < 0.05) with working memory and information processing speed, as measured by the Symbol-Digit Modalities Test.Conclusion: T1-RT in the cortex and thalamus correlate with information processing speed in patients with MS.

Highlights

  • Magnetic resonance imaging is an established tool to help diagnose and monitor inflammatory disease progression in multiple sclerosis (MS) [1]

  • T1 relaxation times (T1-RT) in the cortex and thalamus correlate with information processing speed in patients with MS

  • Besides inflammatory processes affecting the white matter (WM), gray matter (GM) involvement has been shown to be extensive in MS and is associated with clinical disability [3,4,5]

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Summary

Introduction

Magnetic resonance imaging is an established tool to help diagnose and monitor inflammatory disease progression in multiple sclerosis (MS) [1]. Besides inflammatory processes affecting the WM, gray matter (GM) involvement has been shown to be extensive in MS and is associated with clinical disability [3,4,5]. Diffuse gray matter injury in the thalamus, caused by demyelination and secondary degeneration, is recognized to contribute to cognitive impairment in patients with MS [6, 7]. These histopathological processes are often subtle and difficult to detect with conventional MRI protocols. Cortical and thalamic pathologies have been associated with cognitive impairment in patients with multiple sclerosis (MS)

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