Relationship between brain MRI lesion load and short-term disease evolution in non-disabling MS: a large-scale, multicentre study

Author:

Rovaris Marco1,Rocca Maria A1,Barkhof Frederik2,Calabrese Massimiliano3,De Stefano Nicola4,Khalil Michael5,Fazekas Franz5,Fisniku Leonora6,Gallo Paolo3,Miller David H6,Montalban Xavier7,Polman Chris8,Rovira Alex9,Sombekke Madeleine H8,Sormani Maria Pia10,Stromillo Maria Laura4,Filippi Massimo1

Affiliation:

1. Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, Scientific Institute and University Hospital San Raffaele, Italy.

2. Department of Neuroradiology, VU University Medical Centre, The Netherlands.

3. MS Centre of Veneto Region, Department of Neurosciences, University Hospital, Italy.

4. Department of Neurology, University of Siena, Italy.

5. Department of Neurology, Medical University of Graz, Austria.

6. MS NMR Research Unit, Institute of Neurology, University College London, UK.

7. Department of Neuroimmunology, Hospital Vall d’Hebron, Spain.

8. Department of Neurology, VU University Medical Centre, The Netherlands.

9. Department of Radiology, Hospital Vall d’Hebron, Spain.

10. DISSAL, Unit of Biostatistics, University of Genoa, Italy.

Abstract

Background and Objectives: We evaluated clinical and conventional MRI features of a large population of patients with non-disabling MS to identify potential markers of a benign disease course. Methods: In seven MAGNIMS centres we retrospectively identified 182 patients with benign (B) MS (EDSS score ≤3.0, disease duration ≥15 years) and 187 patients with non-disabling relapsing–remitting MS (NDRRMS) (Expanded Disability Status Scale score ≤3.0, disease duration between 5 and 14 years), in whom clinical data were collected within two weeks from a brain T2-weighted scan. Brain T2 lesion volume (LV) was measured in all patients. In 146 BMS and 146 NDRRMS patients, clinical data were also available after a median follow up of 29 months (range: 7–104 months). Results: Mean LV was higher in BMS than in NDRRMS patients ( p < 0.001), but the mean ratio between LV and disease duration was higher in NDRRMS than in BMS patients (1.1 vs. 0.6 ml/year, p < 0.001). In BMS patients, brain LV was correlated with EDSS score increase at follow up ( r = 0.18, p = 0.03). Conclusions: An overall low rate of brain LV increase during a long-lasting disease course might be a feature of BMS. In BMS patients, a high brain LV might be associated with worsening of locomotor disability at short-term follow up.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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