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  3. Corpus callosum index and long-term disability in multiple sclerosis patients
 

Corpus callosum index and long-term disability in multiple sclerosis patients

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BORIS DOI
10.48350/256
Date of Publication
2010
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Yaldizli, Ozgür
Atefy, Ramir
Universitätsklinik für Neurologie
Gass, Achim
Sturm, Dietrich
Glassl, Stephanie
Tettenborn, Barbara
Putzki, Norman
Series
Journal of neurology
ISSN or ISBN (if monograph)
0340-5354
Publisher
Springer-Medizin-Verlag
Language
English
Publisher DOI
10.1007/s00415-010-5503-x
PubMed ID
20198382
Description
Prediction of long-term disability in patients with multiple sclerosis (MS) is essential. Magnetic resonance imaging (MRI) measurement of brain volume may be of predictive value but sophisticated MRI techniques are often inaccessible in clinical practice. The corpus callosum index (CCI) is a normalized measurement that reflects changes of brain volume. We investigated medical records and 533 MRI scans at diagnosis and during clinical follow-up of 169 MS patients (mean age 42 +/- 11 years, 86% relapsing-remitting MS, time since first relapse 11 +/- 9 years). CCI at diagnosis was 0.345 +/- 0.04 and correlated with duration of disease (p = 0.002; r = -0.234) and expanded disability status scale (EDSS) score at diagnosis (r = -0.428; p < 0.001). Linear regression analyses identified age, duration of disease, relapse rate and EDSS at diagnosis as independent predictors for disability after mean of 7.1 years (Nagelkerkes' R:0.56). Annual CCI decrease was 0.01 +/- 0.02 (annual tissue loss: 1.3%). In secondary progressive MS patients, CCI decrease was double compared to that in relapsing-remitting MS patients (p = 0.04). There was a trend of greater CCI decrease in untreated patients compared to those who received disease modifying drugs (p = 0.2). CCI is an easy to use MRI marker for estimating brain atrophy in patients with MS. Brain atrophy as measured with CCI was associated with disability progression but it was not an independent predictor of long-term disability.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/71050
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