Temporal changes and geographical differences in multiple sclerosis phenotypes in Japanese: nationwide survey results over 30 years

Author:

Osoegawa M1,Kira J1,Fukazawa T2,Fujihara K3,Kikuchi S4,Matsui M5,Kohriyama T6,Sobue G7,Yamamura T8,Itoyama Y3,Saida T9,Sakata K10,Ochi H1,Matsuoka T1,

Affiliation:

1. Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan

2. Department of Neurology, Nishimaruyama Hospital, Sapporo, Japan

3. Department of Neurology, Tohoku University School of Medicine, Sendai, Japan

4. Department of Neurology, Sapporo-Minami National Hospital, Sapporo, Japan

5. Department of Neurology, Kanazawa Medical University, Kanazawa, Japan

6. Department of Clinical Neuroscience and Therapeutics, Division of Integrated Medical Science, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan

7. Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan

8. Department of Immunology, National Institute of Neuroscience, NCNP, Tokyo, Japan

9. Department of Neurology, Center for Neurological Diseases, Utano National Hospital, Kyoto, Japan

10. Department of Hygiene and Preventive Medicine, Iwate Medical University School of Medicine, Morioka, Japan

Abstract

Background There are two distinct phenotypes of multiple sclerosis (MS) in Asians, manifesting as optic-spinal (OSMS) and conventional (CMS) forms. In Japan, four nationwide surveys of MS have been conducted. The first three were in 1972, 1982, and 1989, and we performed the fourth in 2004. Results The recent survey showed six main findings as follows: (1) a four-fold increase in the estimated number of clinically definite patients with MS in 2003 (9900; crude MS prevalence, 7.7/100,000) compared with 1972; (2) a shift in the peak age at onset from early 30s in 1989 to early 20s in 2003; (3) a successive proportional decrease in optic-spinal involvement in clinically definite patients with MS; (4) a significant north–south gradient for the CMS/OSMS ratio; (5) after subdivision of the mainland (30–45° North) into northern and southern parts at 37°N, northern-born northern residents (northern patients) showed a significantly higher CMS/OSMS ratio and higher frequency of brain lesions fulfilling the Barkhof criteria (Barkhof brain lesions) than southern-born southern residents (southern patients); (6) among northern patients, the absolute numbers of patients with CMS and those with Barkhof brain lesions rapidly increased with advancing birth year. Conclusions These findings suggest that MS phenotypes are drastically altered by environmental factors, such as latitude and “Westernization.”

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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