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October 19, 2010; 75 (16) Articles

IFNβ-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum

J. Shimizu, Y. Hatanaka, M. Hasegawa, A. Iwata, I. Sugimoto, H. Date, J. Goto, T. Shimizu, M. Takatsu, Y. Sakurai, H. Nakase, Y. Uesaka, H. Hashida, K. Hashimoto, T. Komiya, S. Tsuji
First published September 8, 2010, DOI: https://doi.org/10.1212/WNL.0b013e3181f8832e
J. Shimizu
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Y. Hatanaka
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M. Hasegawa
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A. Iwata
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I. Sugimoto
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H. Date
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J. Goto
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T. Shimizu
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M. Takatsu
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Y. Sakurai
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H. Nakase
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Y. Uesaka
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H. Hashida
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K. Hashimoto
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T. Komiya
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S. Tsuji
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Citation
IFNβ-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum
J. Shimizu, Y. Hatanaka, M. Hasegawa, A. Iwata, I. Sugimoto, H. Date, J. Goto, T. Shimizu, M. Takatsu, Y. Sakurai, H. Nakase, Y. Uesaka, H. Hashida, K. Hashimoto, T. Komiya, S. Tsuji
Neurology Oct 2010, 75 (16) 1423-1427; DOI: 10.1212/WNL.0b013e3181f8832e

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Abstract

Background: Interferon-β-1b (IFNβ-1b) has been used to prevent exacerbation of relapsing-remitting multiple sclerosis (RRMS) including optic-spinal multiple sclerosis (OSMS) in Japan. We encountered 2 patients with OSMS with unexpectedly severe exacerbation soon after the initiation of IFNβ-1b therapy. The experience urged us to retrospectively review the patients with RRMS who had been treated with IFNβ-1b to identify similar cases.

Methods: At neurologic departments of 9 hospitals, the medical records of 56 patients with RRMS were reviewed to identify those who showed severe exacerbation soon after the initiation of IFNβ-1b therapy.

Results: Of 56 patients with RRMS, we identified 7 who experienced severe exacerbation (exacerbation with increased scores of Expanded Disability Status Scale ≧7.0) within 90 days of the initiation of IFNβ-1b therapy. In all 7 patients, the exacerbations after the initiation of IFNβ-1b therapy were more severe than those experienced by the individual patients before the use of IFNβ-1b, and seemed to have occurred unexpectedly in a short time after the initiation of INFβ-1b therapy. A retrospective analysis revealed that all 7 patients had antibodies toward aquaporin 4, and the clinical features of all 7 patients after the exacerbation were consistent with those of neuromyelitis optica (NMO) spectrum.

Conclusions: Our study suggests that IFNβ-1b may trigger severe exacerbation in patients with the NMO spectrum. In INFβ-1b therapy, cases in NMO spectrum should be carefully excluded.

Footnotes

  • Study funding: Supported by Grants-in-Aid for Scientific Research and Health and Labour Sciences Research Grants for Research on Intractable Diseases from the Ministry of Health, Labour and Welfare of Japan.

  • AQP4
    aquaporin 4
    CMS
    conventional multiple sclerosis
    cRRMS
    RRMS not meeting the criteria of NMO
    EDSS
    Expanded Disability Status Scale
    IFNβ-1b
    interferon-β-1b
    LESCL
    longitudinally extensive spinal cord lesion
    MS
    multiple sclerosis
    NMO
    neuromyelitis optica
    OSMS
    optic-spinal multiple sclerosis
    RRMS
    relapsing-remitting multiple sclerosis

  • Editorial, page 1404

  • Supplemental data at www.neurology.org

  • Received January 10, 2010.
  • Accepted June 7, 2010.
  • Copyright © 2010 by AAN Enterprises, Inc.
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Letters: Rapid online correspondence

  • IFNβ-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum
    • Roberto Bomprezzi, Barrow Neurological Institute, 500 W. Thomas Rd, Suite 300, Phoenix, AZ 85013rbomprezzi@chw.edu
    • J. Michael Powers, MD
    Submitted February 17, 2011
  • Reply from the authors
    • Jun Shimizu MD, PhD, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japanshimizu-neu@h.u-tokyo.ac.jp
    • Shoji Tsuji MD PhD
    Submitted February 17, 2011
  • Reply from the Editorialists
    • Brian G. Weinshenker, Department of Neurology, Mayo Clinic, Rochester, MNweinb@mayo.edu
    • Dean M. Wingerchuk
    Submitted February 17, 2011
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