Data supporting information.

BackgroundQuantitative T1 mapping is a valuable technique for assessing tissue injury in multiple sclerosis (MS) lesions. We previously introduced a novel methodology for converting high-resolution anatomical 3D T1-weighted (T1W) images into parametric T1 relaxometry maps. Herein, we correlate MS lesion pathology as quantified by retroactive T1 mapping with clinical and MRI metrics of disability and with magnetization transfer ratio (MTR).Methods38 subjects with relapsing-remitting MS (RRMS) were examined, contributing to 587 unique lesions for analysis. T1 and MTR values were compared using correlation statistics. Univariate correlations between lesional T1 or MTR and Expanded Disability Status Scale (EDSS) were examined using Spearman’s rho (ρ), and for disease duration and brain parenchymal fraction (BPF), Pearson’s r. Mean T1 values of lesions were compared across different categories of EDSS severity using Kruskal-Wallis test. Ordinal regression model was used to assess the association between EDSS and T1 values of select brain regions.ResultsThe mean T1 of lesions showed a high correlation with - MTR, r = 0.68. T2 lesion volumes stratified based on different T1 thresholds showed a significant correlation with MS disease metrics: lesion volume threshold at 700 1100 was correlated with EDSS (ρ = 0.41, p = 0.01), disease duration (r = 0.45, p = 0.001), and BPF (r = -0.51, p th, 50th, and 75th percentiles significantly correlated with BPF (r = -0.41, p = 0.01; r = -0.41, p = 0.01; r = -0.38, p = 0.02). MTR showed a significant correlation with EDSS but not with disease duration or BPF. Mean T1 values in the NAWM showed a significant association with EDSS (coefficient = 0.03, pseudo R2 = 0.07, p = 0.03).ConclusionsWe provide clinical validation of retroactive T1 mapping as a complementary post-processing technique for monitoring disease activity and disability progression in MS.