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根据第四次全国性调查结果,日本多发性硬化症表型的异质性和连续性

Heterogeneity and continuum of multiple sclerosis phenotypes in Japanese according to the results of the fourth nationwide survey.

作者信息

Ishizu Takaaki, Kira Jun-ichi, Osoegawa Manabu, Fukazawa Toshiyuki, Kikuchi Seiji, Fujihara Kazuo, Matsui Makoto, Kohriyama Tatsuo, Sobue Gen, Yamamura Takashi, Itoyama Yasuto, Saida Takahiko, Sakata Kiyomi

机构信息

Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, 3-1-1Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

J Neurol Sci. 2009 May 15;280(1-2):22-8. doi: 10.1016/j.jns.2009.01.008. Epub 2009 Feb 7.

Abstract

There are two distinct phenotypes of multiple sclerosis (MS) in Asians, optic-spinal MS (OSMS) and conventional MS (CMS). In 2004, we performed the fourth nationwide epidemiological survey of MS. The epidemiological features were reported elsewhere; here we report the characteristic features of patients with each MS phenotype, classified according to the clinically estimated sites of involvement and MRI findings. Among 1493 MS patients collated, 57.7% were classified as having CMS and 16.5% were classified as having OSMS. Based on MRI findings, MS patients were further subdivided into those with OSMS with or without longitudinally extensive spinal cord lesions (LESCLs) and those with CMS with or without LESCLs. Although disease duration did not differ significantly among the four groups, EDSS scores were significantly higher in patients with LESCLs than in those without LESCLs, irrespective of OSMS or CMS phenotype. Similar trends were found for the frequencies of bilateral visual loss, transverse myelitis, and marked CSF pleocytosis and neutrophilia. Increased IgG index, brain lesions fulfilling the Barkhof criteria and secondary progression were more commonly found in CMS patients than in OSMS patients, while negative brain MRIs were more commonly encountered in OSMS patients than CMS patients, irrespective of the presence of LESCLs. These findings suggest that demographic features not only vary based on CMS or OSMS phenotype, but also with the presence or absence of LESCLs, and that nonetheless, these four phenotypes constitute a continuum.

摘要

亚洲人中的多发性硬化症(MS)有两种不同的表型,即视神经脊髓型MS(OSMS)和经典型MS(CMS)。2004年,我们开展了第四次全国性MS流行病学调查。流行病学特征已在其他地方报道;在此我们报告根据临床估计的受累部位和MRI结果分类的每种MS表型患者的特征。在整理的1493例MS患者中,57.7%被分类为患有CMS,16.5%被分类为患有OSMS。基于MRI结果,MS患者进一步细分为有或无纵向广泛脊髓病变(LESCLs)的OSMS患者以及有或无LESCLs的CMS患者。尽管四组之间病程无显著差异,但无论OSMS或CMS表型如何,有LESCLs的患者的扩展残疾状态量表(EDSS)评分显著高于无LESCLs的患者。双侧视力丧失、横贯性脊髓炎以及明显的脑脊液淋巴细胞增多和中性粒细胞增多的频率也发现了类似趋势。与OSMS患者相比,CMS患者更常出现IgG指数升高、符合Barkhof标准的脑病变和继发进展,而无论是否存在LESCLs,OSMS患者比CMS患者更常出现脑MRI阴性。这些发现表明,人口统计学特征不仅因CMS或OSMS表型而异,还因有无LESCLs而异,尽管如此,这四种表型构成一个连续统一体。

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