Rapid disease course in African Americans with multiple sclerosis
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Abstract
Objective: To investigate utility of a Multiple Sclerosis Severity Scale (MSSS)–based classification system for comparing African American (AA) and white American (WA) multiple sclerosis (MS) subpopulations in the New York State Multiple Sclerosis Consortium (NYSMSC) database. MSSS is a frequency-rank algorithm relating MS disability to disease duration in a large, untreated reference population.
Design/Methods: Distributions of patients in 6 MSSS-based severity grades were calculated for AA and WA registrants.
Results: There were 419 AA and 5,809 WA patients in the NYSMSC, who had EDSS recorded during years 1–30 since symptom onset. Median EDSS was not different in AA and WA (3.5 vs 3.0, p = 0.60), whereas median MSSS in AA was higher than in WA (6.0 vs 4.8, p = 0.001). AA patients were overrepresented in the 2 most severe grades (41.5% vs 29.3% for WA) and underrepresented in the 2 lowest grades (23.4% vs 35.4%; p < 0.001). In multivariable analysis (ordered logistic and median regression), MSSS for AA remained significantly higher than in WA after adjusting for age, gender, disease duration, disease type distribution, and treatment with disease-modifying therapies.
Conclusions: The 6-tiered MSSS grading system is a powerful tool for comparing rate of disease progression in subpopulations of interest. MSSS-based analysis demonstrates that African ancestry is a risk factor for a more rapidly disabling disease course.
Footnotes
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Study funding: Supported by an independent medical research grant from EMD Serono/Pfizer Inc.
Disclosure: Author disclosures are provided at the end of the article.
Received November 24, 2009. Accepted in final form March 24, 2010.
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