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Factors associated with benign multiple sclerosis in the New York State MS Consortium (NYSMSC).
Zivadinov, Robert; Cookfair, Diane L; Krupp, Lauren; Miller, Aaron E; Lava, Neil; Coyle, Patricia K; Goodman, Andrew D; Jubelt, Burk; Lenihan, Michael; Herbert, Joseph; Gottesman, Malcolm; Snyder, David H; Apatoff, Brian R; Teter, Barbara E; Perel, Allan B; Munschauer, Frederick; Weinstock-Guttman, Bianca.
Afiliación
  • Zivadinov R; Buffalo Neuroimaging Analysis Center, Department of Neurology, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA. rzivadinov@bnac.net.
  • Cookfair DL; Department of Neurology, School of Medicine and Biomedical Sciences, University at Buffalo, 100 High Street, Buffalo, NY, 14203, USA. rzivadinov@bnac.net.
  • Krupp L; Department of Neurology, School of Medicine and Biomedical Sciences, University at Buffalo, 100 High Street, Buffalo, NY, 14203, USA.
  • Miller AE; Department of Neurology, Stony Brook University Medical Center, Stony Brook, NY, USA.
  • Lava N; The Corinne Goldsmith Dickinson Center of Multiple Sclerosis, Mount Sinai School of Medicine, New York, NY, USA.
  • Coyle PK; Department of Neurology, Albany Medical School, Multiple Sclerosis Center, Albany, NY, USA.
  • Goodman AD; Department of Neurology, Stony Brook University Medical Center, Stony Brook, NY, USA.
  • Jubelt B; Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
  • Lenihan M; Department of Neurology, SUNY Upstate Medical University, Syracuse, NY, USA.
  • Herbert J; Adirondack Neurology Associates, Glens Falls, NY, USA.
  • Gottesman M; Department of Neurology, NYU School of Medicine, New York, NY, USA.
  • Snyder DH; Department of Neuroscience, Winthrop University Hospital, Mineola, NY, USA.
  • Apatoff BR; Department of Neurology, Weill Medical College of Cornell University, New York, NY, USA.
  • Teter BE; Department of Neurology, Albert Einstein College of Medicine, New York, NY, USA.
  • Perel AB; Multiple Sclerosis Center, New York, NY, USA.
  • Munschauer F; Department of Neurology, School of Medicine and Biomedical Sciences, University at Buffalo, 100 High Street, Buffalo, NY, 14203, USA.
  • Weinstock-Guttman B; Alpha Neurology, Staten Island, NY, USA.
BMC Neurol ; 16: 102, 2016 Jul 15.
Article en En | MEDLINE | ID: mdl-27416843
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos