MRI of the corpus callosum in multiple sclerosis: association with disability

Author:

Ozturk A.1,Smith SA2,Gordon-Lipkin EM3,Harrison DM3,Shiee N.4,Pham DL1,Caffo BS5,Calabresi PA3,Reich DS6

Affiliation:

1. Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA

2. Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA, FM Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, USA

3. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA

4. Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD, USA

5. Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA

6. Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA, FM Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, USA, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA, Translational Neuroradiology Unit, NIH/NINDS, Bethesda, MD, USA,

Abstract

Inflammatory demyelination and axon damage in the corpus callosum are prominent features of multiple sclerosis (MS) and may partially account for impaired performance on complex tasks. The objective of this article was to characterize quantitative callosal MRI abnormalities and their association with disability. In 69 participants with MS and 29 healthy volunteers, lesional and extralesional callosal MRI indices were estimated via diffusion tensor tractography. expanded disability status scale (EDSS) and MS functional composite (MSFC) scores were recorded in 53 of the participants with MS. All tested callosal MRI indices were diffusely abnormal in MS. EDSS score was correlated only with age (r = 0.51). Scores on the overall MSFC and its paced serial auditory addition test (PASAT) and 9-hole peg test components were correlated with callosal fractional anisotropy (r = 0.27, 0.35, and 0.31, respectively) and perpendicular diffusivity (r = —0.29, —0.30, and —0.31) but not with overall callosal volume or callosal lesion volume; the PASAT score was more weakly correlated with callosal magnetization-transfer ratio (r = 0.21). Anterior callosal abnormalities were associated with impaired PASAT performance and posterior abnormalities with slow performance on the 9-hole peg test. In conclusion, abnormalities in the corpus callosum can be assessed with quantitative MRI and are associated with cognitive and complex upper-extremity dysfunction in MS.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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