Comparative Effects of Disease-modifying Therapies on Cognition, Retinal and Clinical Outcomes in African American and Non-African American Patients with Multiple Sclerosis: A 24-month Prospective Study
Brenda Ropero1, Jennifer Kalina2, Zhaonan Sun2, Nicholas Belviso2, Babak Amerian-Williams2, Sai Shankar2, James Lewin2, Daniel Becker3
1International Neurorehabilitation Institute, 2Biogen, 3International Neurorehabilitation Institute, Johns Hopkins Hospital
Objective:

To assess the effects of DMTs on cognition, retinal integrity, fatigue, and EDSS, over 24 months in African American and non-African American patients with relapsing MS.

Background:

Disability, cognitive, visual and fatigue-related impairments are major manifestations of multiple sclerosis (MS) that accumulate more rapidly among African Americans compared to non-African Americans. Despite this, African Americans remain underrepresented in MS clinical studies. Addressing this gap is essential to advance equitable, evidence-based MS care.

Design/Methods:

This prospective, 24-month observational study evaluated African American and Non-African American patients with relapsing MS receiving DMTs. Cognition was assessed using CogEval and NeuroTrax; retinal nerve fiber layer (RNFL) and ganglion cell-inner plexiform (GCIP) thickness were measured using Optical Coherence Tomography; fatigue with the Modified Fatigue Impact Scale (MFIS); and disability using Expanded Disability Status Scale (EDSS). Longitudinal outcomes and racial differences were analyzed using linear mixed-effects models with fixed effects for race, time, and their interaction, adjusting for covariates. Time-varying factors and multiple comparison-corrected contrasts assessed within- and between-group differences.

Results:
A total of 48 patients with relapsing MS (mean age 44 years; 67% female; 54% African American) were followed for 24 months.  No statistically significant racial differences were observed in changes in cognitive scores, retinal layer thickness or fatigue from baseline to 24 months (p>0.05 for all). The African American cohort showed greater within-group improvement in NeuroTrax scores at 12 and 24 months (p<0.01). EDSS scores remained higher among African American patients (p=0.03-0.04), with no significant change over time
Conclusions:

DMT use may confer greater benefit on cognitive outcomes in African American MS patients, while maintaining retinal integrity, and fatigue in African American and non-African American MS patients, underscoring the importance of inclusive research, support treatment strategies for racial groups with MS, and suggest that DMT use can help mitigate disparities in MS outcomes.

10.1212/WNL.0000000000217201
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