Cortical lesion hotspots and association of subpial lesions with disability in multiple sclerosis

Author:

Beck Erin S1ORCID,Maranzano Josefina2,Luciano Nicholas J3,Parvathaneni Prasanna3,Filippini Stefano34,Morrison Mark3,Suto Daniel J3,Wu Tianxia3,van Gelderen Peter3,de Zwart Jacco A3ORCID,Antel Samson5,Fetco Dumitru5,Ohayon Joan3,Andrada Frances3,Mina Yair36,Thomas Chevaz3,Jacobson Steve3,Duyn Jeff3,Cortese Irene3,Narayanan Sridar5,Nair Govind3,Sati Pascal37ORCID,Reich Daniel S3ORCID

Affiliation:

1. National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA

2. McConnell Brain Imaging Centre, Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada; Department of Anatomy, University of Quebec in Trois-Rivières, Trois-Rivières, QC, Canada

3. National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA

4. Department of Neurosciences, Drug and Child Health, University of Florence, Florence, Italy

5. McConnell Brain Imaging Centre, Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada

6. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

7. Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA, USA

Abstract

Background: Dramatic improvements in visualization of cortical (especially subpial) multiple sclerosis (MS) lesions allow assessment of impact on clinical course. Objective: Characterize cortical lesions by 7 tesla (T) T2*-/T1-weighted magnetic resonance imaging (MRI); determine relationship with other MS pathology and contribution to disability. Methods: Sixty-four adults with MS (45 relapsing–remitting/19 progressive) underwent 3 T brain/spine MRI, 7 T brain MRI, and clinical testing. Results: Cortical lesions were found in 94% (progressive: median 56/range 2–203; relapsing–remitting: 15/0–168; p = 0.004). Lesion distribution across 50 cortical regions was nonuniform ( p = 0.006), with highest lesion burden in supplementary motor cortex and highest prevalence in superior frontal gyrus. Leukocortical and white matter lesion volumes were strongly correlated ( r = 0.58, p < 0.0001), while subpial and white matter lesion volumes were moderately correlated ( r = 0.30, p = 0.002). Leukocortical ( p = 0.02) but not subpial lesions ( p = 0.40) were correlated with paramagnetic rim lesions; both were correlated with spinal cord lesions ( p = 0.01). Cortical lesion volumes (total and subtypes) were correlated with expanded disability status scale, 25-foot timed walk, nine-hole peg test, and symbol digit modality test scores. Conclusion: Cortical lesions are highly prevalent and are associated with disability and progressive disease. Subpial lesion burden is not strongly correlated with white matter lesions, suggesting differences in inflammation and repair mechanisms.

Funder

National Institute of Neurological Disorders and Stroke

National Multiple Sclerosis Society

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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