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[室户病或日本纪伊半岛肌萎缩侧索硬化-帕金森综合征-痴呆复合征]

[Muro disease or ALS-parkinsonism-dementia complex of the Kii peninsula of Japan].

作者信息

Kuzuhara Shigeki

机构信息

Department of Neurology, Mie University School of Medicine.

出版信息

Rinsho Shinkeigaku. 2007 Nov;47(11):695-702.

PMID:18210779
Abstract

"Muro disease" is an endemic ALS in the Muro district that includes the southern coastal mountainous areas of the Kii peninsula of Japan. Epidemiological survey in 1960s disclosed extremely high incidence of ALS in two villages, Hohara and Kozagawa, and disappearance of high incidence by early 1980s was reported with its etiology unsolved. We resurveyed for neurodegenerative diseases in Hohara and found continuous high ALS incidence. We also found parkinsonism-dementia complex (PDC) verified neuropathologically. ALS and PDC frequently occurred in one individual simultaneously and affected many members in the same family, and neuropathological findings of ALS and PDC were similar to each other, showing a combination of upper and lower motor neuron involvements and many neurofibrillar tangles (NFTs) in the brainstem and cerebral cortex, resembling those of ALS/PDC on Guam. TDP-43 positive inclusions were found in the dentate gyrus of the hippocampus and spinal motor neurons in all cases examined. Age-adjusted incidence rates during 1950 and 2000 have showed that incidence of ALS was gradually declining for 50 years while that of PDC rose up steeply in 1990s. No particular environmental factors were confirmed and gene analyses of candidate genes of ALS, parkinsonism and dementia failed to reveal any mutations. Continuing high incidence and high rates of familial occurrence suggest that primary cause of Kii ALS/PDC may be genetic rather than environmental.

摘要

“室户病”是室户地区的一种地方性肌萎缩侧索硬化症,该地区包括日本纪伊半岛南部沿海山区。20世纪60年代的流行病学调查显示,在小原和小川这两个村庄,肌萎缩侧索硬化症的发病率极高,到20世纪80年代初报告称高发病率消失,但其病因尚未解决。我们对小原的神经退行性疾病进行了重新调查,发现肌萎缩侧索硬化症的发病率持续居高不下。我们还发现了经神经病理学证实的帕金森痴呆综合征(PDC)。肌萎缩侧索硬化症和帕金森痴呆综合征经常在同一个体中同时出现,并影响同一家族中的许多成员,而且肌萎缩侧索硬化症和帕金森痴呆综合征的神经病理学表现彼此相似,显示出上下运动神经元均受累,并且在脑干和大脑皮层中有许多神经原纤维缠结(NFTs),类似于关岛的肌萎缩侧索硬化症/帕金森痴呆综合征。在所检查的所有病例中,在海马齿状回和脊髓运动神经元中均发现了TDP - 43阳性包涵体。1950年至2000年期间的年龄调整发病率表明,肌萎缩侧索硬化症的发病率在50年中逐渐下降,而帕金森痴呆综合征的发病率在20世纪90年代急剧上升。未确认任何特定的环境因素,对肌萎缩侧索硬化症、帕金森症和痴呆症候选基因的基因分析也未发现任何突变。持续的高发病率和高家族发病率表明,纪伊肌萎缩侧索硬化症/帕金森痴呆综合征的主要病因可能是遗传而非环境因素。

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