Relevance of hypointense brain MRI lesions for long-term worsening of clinical disability in relapsing multiple sclerosis

Author:

Giorgio Antonio1,Stromillo Maria Laura1,Bartolozzi Maria Letizia2,Rossi Francesca1,Battaglini Marco1,De Leucio Alessandro1,Guidi Leonello2,Maritato Patrizia2,Portaccio Emilio3,Sormani Maria Pia4,Amato Maria Pia3,De Stefano Nicola1

Affiliation:

1. Department of Neurological and Behavioral Sciences, University of Siena, Italy

2. Neurology Unit, Hospital of Empoli, Italy

3. Department of Neurology, University of Florence, Italy

4. Department of Health Sciences (DISSAL), University of Genoa, Italy

Abstract

Background: The accrual of brain focal pathology is considered a good substrate of disability in relapsing–remitting multiple sclerosis (RRMS). However, knowledge on long-term lesion evolution and its relationship with disability progression is poor. Objective: The objective of this paper is to evaluate in RRMS the long-term clinical relevance of brain lesion evolution. Methods: In 58 RRMS patients we acquired, using the same scanner and protocol, brain magnetic resonance imaging (MRI) at baseline and 10±0.5 years later. MRI data were correlated with disability changes as measured by the Expanded Disability Status Scale (EDSS). Results: The annualized 10-year lesion volume (LV) growth was +0.25±0.5 cm3 (+6.7±8.7%) for T2-weighted (T2-W) lesions and +0.20±0.31 cm3 (+11.5±12.3%) for T1-weighted (T1-W) lesions. The univariate analysis showed moderate correlations between baseline MRI measures and EDSS at 10 years ( p < 0.001). Also, 10-year EDSS worsening correlated with LV growth and the number of new/enlarging lesions measured over the same period ( p < 0.005). In the stepwise multiple regression analysis, EDSS worsening over 10 years was best correlated with the combination of baseline T1-W lesion count and increasing T1-W LV ( R = 0.61, p < 0.001). Conclusion: In RRMS patients, long-term brain lesion accrual is associated with worsening in clinical disability. This is particularly true for hypointense, destructive lesions.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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