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Factors associated with benign multiple sclerosis in the New York State MS Consortium (NYSMSC)

  • Robert Zivadinov
  • , Diane L. Cookfair
  • , Lauren Krupp
  • , Aaron E. Miller
  • , Neil Lava
  • , Patricia K. Coyle
  • , Andrew D. Goodman
  • , Burk Jubelt
  • , Michael Lenihan
  • , Joseph Herbert
  • , Malcolm Gottesman
  • , David H. Snyder
  • , Brian R. Apatoff
  • , Barbara E. Teter
  • , Allan B. Perel
  • , Frederick Munschauer
  • , Bianca Weinstock-Guttman
  • SUNY Buffalo
  • Stony Brook University
  • Icahn School of Medicine at Mount Sinai
  • Albany Medical College
  • University of Rochester
  • SUNY Upstate Medical University
  • Adirondack Neurology Associates
  • New York University
  • Winthrop University Hospital
  • Cornell University
  • Albert Einstein College of Medicine
  • Multiple Sclerosis Center
  • Alpha Neurology

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Background: This retrospective analysis explored prognostic factors associated with a benign multiple sclerosis (BMS) disease course at baseline and over the 4-year follow-up. Methods: Patients from the centralized New York State Multiple Sclerosis Consortium registry were classified as having BMS according to 3 different criteria centered on disease duration and disability. Additional analyses explored prognostic factors associated with BMS using the most conservative disability criteria (Expanded Disability Status Scale ≤2 and disease duration ≥10 years). Results: Among 6258 patients who fulfilled eligibility criteria, 19.8 % to 33.3 % were characterized as having BMS, at baseline depending on classification criteria used. Positive prognostic factors for BMS at baseline included female sex (p < 0.0001) and younger age at onset (p < 0.0001); negative prognostic factors included progressive-onset type of MS and African-American race. Of the 1237 BMS patients (per most conservative criteria), 742 were followed for a median of 4 years to explore effect of disease-modifying treatment (DMT) on benign status. DMT (p = 0.009) and longer disease duration (p = 0.007) were the only significant positive predictors of maintaining BMS at follow-up. The protective effect was stronger for patients taking DMT at both enrollment and follow-up (OR = 0.71; p = 0.006). Conclusions: There is a need for development of more reliable prognostic indicators of BMS. Use of DMT was significantly associated with maintaining a benign disease state.

Original languageEnglish
Article number102
JournalBMC Neurology
Volume16
Issue number1
DOIs
StatePublished - Jul 15 2016

Keywords

  • Benign multiple sclerosis
  • Disease course
  • Disease-modifying treatment
  • DMT
  • Multiple sclerosis

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