Quantitative MRI analysis of cerebral lesions and atrophy in post-partum patients with multiple sclerosis

Objective: To assess the change in cerebral lesions and atrophy associated with pregnancy in patients with multiple sclerosis (MS). Background: Multiple sclerosis often affects women of reproductive age. Disease stabilization typically occurs during pregnancy, with transient recrudescence postpartum. Previous studies showed increased MRI-defined inflammatory Gadolinium enhancing disease activity and T2 lesion load in the 6 months' post-partum. The effect of pregnancy on T1 lesion load and brain atrophy in MS is not well understood. Methods: We retrospectively identified 16 patients with relapsing-2remitting MS (ARMS) with pre-pregnancy and post-partum 1.5 T brain MRI separated by (mean +/- SD) 15.4 +/- 3.2 months. The time between delivery and post-partum MRI was 2.2 +/- 1.5 months. Baseline characteristics were age 33.0 +/- 4.1 years, disease duration 7.2 +/- 4.8 years, and Expanded Disability Status Score (EDSS) 1.0 +/- 1.0. T2 hyperintense (T2LV) and T1 hypointense (T1LV) lesion volumes were quantified and the number of Gd + lesions was assessed. An SPM12 pipeline estimated global atrophy using brain parenchymal fraction (BPF) and global cortical gray matter (GM) atrophy using the cortical GM fraction (cGMF). Paired t-tests assessed within subject changes. Spearman's correlation coefficients assessed MRI-clinical associations. Results: Post-partum, there was an increase in both T1LV (p = .048, p = .023 with cube root transformation (CRT) and T2LV (p = .022, CRT p = .065). There were no changes in Gd + lesions, BPF, or cGMF (all p > .05). Conclusions: Pregnancy is associated with increased in T2 and T1 cerebral lesion load in MS. However, a de-coupling is apparent, with no whole brain or cortical atrophy developing despite the increase in destructive lesions and despite the expected pregnancy-related decline in brain volume. While in the short term, pregnancy may be protective against the brain volume loss expected with increased lesion load, longer duration of follow-up is needed to verify these findings.