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[阿尔茨海默病研究进展——综述]

[Advances in the research on Alzheimer's disease--overview].

作者信息

Tsuji S

机构信息

Department of Neurology, Niigata University.

出版信息

Rinsho Shinkeigaku. 1997 Dec;37(12):1093-4.

PMID:9577653
Abstract

The number of patients suffering from dementia in Japan has been estimated to exceed 1,250,000 and is expected to increase rapidly in the near future. It is quickly becoming a serious medical and social issue. Alzheimer's disease (AD) is a leading cause of dementia, and can be classified into two genetic categories: single-gene and polygenic diseases. Familial Alzheimer's disease (FAD) is classified as a single-gene disease, while sporadic AD is classified as a polygenic disease which involves multiple genetic and environmental factors. Using positional cloning, most of the genes which lead to FAD have recently been identified e.g., the amyloid precursor protein (APP) gene on chromosome 21, presenilin I on chromosome 14 and presenilin II on chromosome 1. Recent studies indicate that mutations in these genes can result in either overproduction of A beta or in production of A beta 1-42. Although the accumulation of A beta has been suggested to be the "primary cause" not only in FAD but also in sporadic AD, it remains unclear how neurodegeneration in AD is related to the accumulation of A beta. The discovery of ApoE4 as a major genetic risk factor for AD has created a new step of research on AD as a polygenic disease. Although it is confirmed that the presence of the ApoE4 allele greatly accelerates age at onset of AD, the role of ApoE4 as a risk factor for AD remains to be fully elucidated. Now that major genes involved in the pathogenesis of AD have been identified, future research should be directed toward elucidation of the molecular mechanisms of how these gene products are involved in the pathogenesis of AD on protein as well as cellular levels.

摘要

据估计,日本患有痴呆症的患者人数已超过125万,并且预计在不久的将来会迅速增加。这正迅速成为一个严重的医学和社会问题。阿尔茨海默病(AD)是痴呆症的主要病因,可分为两种遗传类型:单基因疾病和多基因疾病。家族性阿尔茨海默病(FAD)被归类为单基因疾病,而散发性AD被归类为涉及多种遗传和环境因素的多基因疾病。利用定位克隆技术,最近已鉴定出大多数导致FAD的基因,例如21号染色体上的淀粉样前体蛋白(APP)基因、14号染色体上的早老素I和1号染色体上的早老素II。最近的研究表明,这些基因中的突变可导致β-淀粉样蛋白(Aβ)过量产生或产生Aβ1-42。尽管已有人提出Aβ的积累不仅是FAD也是散发性AD的“主要病因”,但AD中的神经退行性变与Aβ积累之间的关系仍不清楚。载脂蛋白E4(ApoE4)作为AD的主要遗传风险因素的发现为AD作为一种多基因疾病的研究开创了新的阶段。尽管已证实ApoE4等位基因的存在会大大加速AD的发病年龄,但ApoE4作为AD风险因素的作用仍有待充分阐明。既然已经确定了参与AD发病机制的主要基因,未来的研究应致力于阐明这些基因产物在蛋白质和细胞水平上如何参与AD发病机制的分子机制。

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