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Brain, Vol. 122, No. 9, 1689-1696, September 1999
© 1999 Oxford University Press

HLA-DPB1*0501-associated opticospinal multiple sclerosis

Clinical, neuroimaging and immunogenetic studies

Kenji Yamasaki1, Izumi Horiuchi1, Motozumi Minohara1, Yuji Kawano1, Yasumasa Ohyagi2, Takeshi Yamada1, Futoshi Mihara2, Hiroshi Ito3, Yasuharu Nishimura3 and Jun-ichi Kira1

1 Department of Neurology, Neurological Institute and 2 Department of Radiology, Graduate School of Medical Sciences, Kyushu University and 3 Division of Immunogenetics, Department of Neuroscience and Immunology, Kumamoto University Graduate School of Medical Sciences, Japan

Correspondence to: Dr J. Kira, Department of Neurology, Neurological Institute, Faculty of Medicine, Kyushu University, Fukuoka 812–8582, Japan E-mail: kira{at}neuro.med.kyushu-u.ac.jp

In order to clarify the relationship between the clinical phenotype and the human leucocyte antigen (HLA) in multiple sclerosis in Asians, 93 Japanese patients with clinically definite multiple sclerosis underwent clinical MRI and HLA-DPB1 gene typing studies. According to a neurological examination, 29 patients were classified as opticospinal multiple sclerosis, 17 as spinal multiple sclerosis and 47 as Western type multiple sclerosis showing the involvement of multiple sites in the CNS including either the cerebrum, cerebellum or brainstem. The opticospinal multiple sclerosis showed a significantly higher age of onset, higher expanded disability status scale scores and higher CSF cell counts and protein content than the Western type multiple sclerosis. On brain and spinal cord MRI, the opticospinal multiple sclerosis showed a significantly lower number of brain lesions, but a higher frequency of gadolinium-enhancement of the optic nerve and a higher frequency of spinal cord atrophy than in Western type multiple sclerosis. The frequency of the HLA-DPB1*0501 allele was found to be significantly greater in opticospinal multiple sclerosis (93%) than in healthy controls (63%, corrected P value = 0.0091 and relative risk = 7.9), but not in Western type multiple sclerosis (66%) or spinal multiple sclerosis (82%). The marked differences in the clinical and MRI findings as well as in the immunogenetic backgrounds between the opticospinal multiple sclerosis and Western-type multiple sclerosis together suggest that HLA-DPB1*0501-associated opticospinal multiple sclerosis is a distinct subtype of multiple sclerosis.

multiple sclerosis; human leucocyte antigen; MRI; Asians

EDSS = expanded disability status scale; HLA = human leucocyte antigen; OB = oligoclonal bands; RR = relative risk


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