Skip to main content

Two subtypes of optic-spinal form of multiple sclerosis in Japan: clinical and laboratory features

Abstract

Seventy-seven cases of the optic-spinal form of multiple sclerosis (OSMS) were collected from 6 institutes in 3 cities of Japan, and the clinical and MRI features were analyzed. Two-thirds of the OSMS patients had longitudinally extensive spinal cord MRI lesions (LESL), and had clinical features similar to those of relapsing neuromyelitis optica which often causes severe disability. In contrast, OSMS patients without LESL tended to have milder disease and had some feature commonly seen in the conventional form of MS. The percentage of OSMS without LESL in total OSMS has recently been increasing. The present study suggests that LESL is crucially important for distinguishing the two subtypes of OSMS.

This is a preview of subscription content, access via your institution.

References

  1. Fukazawa T, Tashiro K, Hamada T, Moriwaka F, Matsumoto A, Shima K, Maruo Y (1992) Multiple sclerosis in Hokkaido, the northernmost island of Japan: prospective analyses of clinical features. Intern Med 31:349–352

    PubMed  CAS  Google Scholar 

  2. Fukazawa T (1993) Acute transverse myelopathy in multiple sclerosis: clinical and laboratory analyses. Hokkaido Igaku Zasshi 68:79–95

    PubMed  CAS  Google Scholar 

  3. Fukazawa T, Kikuchi S, Niino M, Yabe I, Miyagishi R, Fukaura H, Hamada T, Tashiro K, Sasaki H (2004) Attack-related severity: a key factor in understanding the spectrum of idiopathic inflammatory demyelinating disorders. J Neurol Sci 225:71–78

    PubMed  Article  CAS  Google Scholar 

  4. Kidd D, Thompson AJ, Kendall BE, Miller DH, McDonald WI (1994) Benign form of multiple sclerosis: MRI evidence for less frequent and less inflammatory disease activity. J Neurol Neurosurg Psychiatry 57:1070–1072

    PubMed  CAS  Article  Google Scholar 

  5. Kikuchi S, Fukazawa T (2005) “OSMS is NMO, but not MS”: confirmed by NMO-IgG? Lancet Neurol 4:594–595

    PubMed  Article  Google Scholar 

  6. Kira J, Yamasaki K, Horiuchi I, Ohyagi Y, Taniwaki T, Kawano Y (1999) Changes in the clinical phenotypes of multiple sclerosis during the past 50 years in Japan. J Neurol Sci 166:53–57

    PubMed  Article  CAS  Google Scholar 

  7. Kira J (2000) A novel feature disclosed in opticospinal multiple sclerosis in Asians. Intern Med 39:272

    PubMed  CAS  Google Scholar 

  8. Kira J (2003) Multiple sclerosis in the Japanese population. Lancet Neurol 2:117–127

    PubMed  Article  Google Scholar 

  9. Lennon VA, Wingerchuk DM, Kryzer TJ, Pittock SJ, Lucchinetti CF, Fujihara K, Nakashima I, Weinshenker BG (2004) A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364:2106–2112

    PubMed  Article  CAS  Google Scholar 

  10. Misu T, Fujihara K, Nakashima I, Miyazawa I, Okita N, Takase S, Itoyama Y (2002) Pure optic-spinal form of multiple sclerosis in Japan. Brain 125:2460–2468

    PubMed  Article  Google Scholar 

  11. Nakashima I, Fujihara K, Takase S, Itoyama Y (1999) Decrease in multiple sclerosis with acute transverse myelitis in Japan. Tohoku J Exp Med 188:89–94

    PubMed  Article  CAS  Google Scholar 

  12. Nakashima I, Fujihara K, Sato S, Itoyama Y (2005) Oligoclonal IgG bands in Japanese patients with multiple sclerosis. A comparative study between isoelectric focusing with IgG immunofixation and high-resolution agarose gel electrophoresis. J Neuroimmunol 159:133–136

    PubMed  Article  CAS  Google Scholar 

  13. Pittock SJ, McClelland RL, Mayr WT, Jorgensen NW, Weinshenker BG, Noseworthy J, Rodriguez M (2004) Clinical implications of benign multiple sclerosis: a 20-year population-based follow-up study. Ann Neurol 56:303–306

    PubMed  Article  Google Scholar 

  14. Saida T, Tashiro K, Itoyama Y, Sato T, Ohashi Y, Zhao Z (2005) Interferon beta-1b is effective in Japanese RRMS patients: a randomized, multicenter study. Neurology 64:621–630

    PubMed  CAS  Google Scholar 

  15. Vitali C, Bombardieri S, Jonsson R, Moutsopoulos HM, Alexander EL, Carsons SE, Daniels TE, Fox PC, Fox RI, Kassan SS, Pillemer SR, Talal N, Weisman MH (2002) Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis 61:554–558

    PubMed  Article  CAS  Google Scholar 

  16. Weinshenker BG (2003) Neuromyelitis optica: what it is and what it might be. Lancet 361:889–890

    PubMed  Article  Google Scholar 

  17. Wingerchuk DM, Hogancamp WF, O’Brien PC, Weinshenker BG (1999) The clinical course of neuromyelitis optica (Devic's syndrome). Neurology 53:1107–1114

    PubMed  CAS  Google Scholar 

  18. Wingerchuk DM, Weinshenker BG (2005) Neuromyelitis Optica. Curr Treat Options Neurol 7:173–182

    PubMed  Google Scholar 

Download references

Author information

Affiliations

Authors

Corresponding author

Correspondence to Ichiro Nakashima MD.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Nakashima, I., Fukazawa, T., Ota, K. et al. Two subtypes of optic-spinal form of multiple sclerosis in Japan: clinical and laboratory features. J Neurol 254, 488–492 (2007). https://doi.org/10.1007/s00415-006-0400-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00415-006-0400-z

Key words

  • multiple sclerosis
  • optic spinal form
  • neuromyelitis optica
  • MRI