Quantitative Measurement of tissue damage and recovery within new T2w lesions in pediatric- and adult-onset multiple sclerosis

Author:

Ghassemi Rezwan1,Brown Robert1,Banwell Brenda2,Narayanan Sridar1,Arnold Douglas L.1,

Affiliation:

1. Montreal Neurological Institute, McGill University, Montreal, QC, Canada

2. The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada; The Children’s Hospital of Philadelphia, Philadelphia, USA

Abstract

Background: Children and adolescents with relapsing–remitting multiple sclerosis (RRMS) have a similar T2 lesion burden as adults matched for disease duration. However, it is unknown whether the degree of tissue destruction within lesions is also similar. Persistent reduced T1-weighted signal intensity within lesions indicates loss of tissue integrity. Objective: We aimed to compare change over a 2-year period in T1 intensity within new T2 lesions, from pre-lesion levels to chronic post-lesion levels, between pediatric and adult-onset MS. Methods: A two-point intensity-normalization method was used to generate normalized T1-weighted (NT1) images from T1-weighted data in 29 pediatric MS patients (age(mean±SD, years), disease duration (years)=15.7±2.4, 3.9±2.6) and 24 adult MS patients (36.7±8.9, 6.9±4.8). Subjects were imaged at three consecutive timepoints, 1 year apart. For each subject, a ‘new-T2’ lesion mask was created and the NT1 intensities ‘pre-lesion’, ‘peri-lesion’ and ‘post-lesion’ were determined. A longitudinal model was used to capture NT1 changes. Results: The NT1 in both groups failed to recover to pre-lesion values by 1 year post-lesion ( p=0.0002), with children showing significantly better recovery than adults ( p=0.0089). Conclusions: Both groups showed a significant chronic reduction of T1 intensity within new T2 lesions. However, children showed a significantly greater recovery of T1 intensity, suggesting that MS lesions in the pediatric MS population are less destructive, or that pediatric patients have greater reparative capacity.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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