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Rapid disease course in African Americans with multiple sclerosis

  • I. Kister
  • , E. Chamot
  • , J. H. Bacon
  • , P. M. Niewczyk
  • , R. A. De Guzman
  • , B. Apatoff
  • , P. Coyle
  • , A. D. Goodman
  • , M. Gottesman
  • , C. Granger
  • , B. Jubelt
  • , L. Krupp
  • , M. Lenihan
  • , F. Lublin
  • , C. Mihai
  • , A. Miller
  • , F. E. Munschauer
  • , A. B. Perel
  • , B. E. Teter
  • , B. Weinstock-Guttman
  • R. Zivadinov, J. Herbert
  • New York University
  • Department of Epidemiology
  • University of Alabama at Birmingham
  • Yeshiva University
  • Uniform Data System for Medical Rehabilitation (UDSMR)
  • Stony Brook University
  • University of Rochester
  • Winthrop University Hospital
  • Multiple Sclerosis Center
  • SUNY Upstate Medical University
  • Glens Falls Neurology
  • Icahn School of Medicine at Mount Sinai
  • Alpha Neurology
  • SUNY Buffalo
  • New York University
  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

122 Scopus citations

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.

Original languageEnglish
Pages (from-to)217-223
Number of pages7
JournalNeurology
Volume75
Issue number3
DOIs
StatePublished - Jul 20 2010

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