和歌山的 C9orf72 重复扩增:日本纪伊半岛肌萎缩侧索硬化症的潜在病因之一

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY
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引用次数: 0

摘要

日本纪伊半岛南部有一组肌萎缩性脊髓侧索硬化症(ALS)病例。虽然遗传和环境因素都被认为是致病原因,但这一病例群的关键病因尚未确定。在欧洲血统的家族性和散发性 C9orf72 相关 ALS 患者中,C9orf72 是最常见的遗传因素,但在日本人群中却很少见。然而,之前的一份报告显示,在集群地区,C9orf72 相关 ALS 的发病率明显较高。我们采用重复引物聚合酶链反应和荧光片段长度分析法,评估了包括集群地区在内的和歌山县确诊的 99 例 ALS 患者中 C9orf72 六核苷酸重复扩增的比例。我们发现,99 例患者中有 2 例(占家族性 ALS 患者的 0%,占散发性 ALS 患者的 2.4%)存在 C9orf72 的六核苷酸重复序列扩增,长序列测序显示这些扩增是致病的。在90名帕金森病患者和90名健康对照者中,均未发现扩增现象。利用长线程测序数据进行的单倍型分析表明,两名重复扩增的患者与之前报道的芬兰 C9orf72 相关 ALS 患者具有共同的单倍型,这表明存在创始效应。C9orf72 在日本被认为是一种罕见的致病基因,但这项研究发现,它在和歌山县可能相对常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C9orf72 repeat expansions in Wakayama: One potential cause of amyotrophic lateral sclerosis in the Kii Peninsula, Japan

A cluster of cases of amyotrophic lateral sclerosis (ALS) exists in the southern part of the Kii Peninsula in Japan. Although both genetic and environmental factors are thought to be causative, the critical cause of this cluster has not been identified. C9orf72 is the most common genetic factor in both familial and sporadic C9orf72-related ALS in people of European ancestry, but it is rare among Japanese populations. However, a previous report revealed that the frequency of C9orf72-related ALS was significantly higher in the cluster area. We evaluated the proportion of C9orf72 hexanucleotide repeat expansions in 99 cases of ALS diagnosed in Wakayama Prefecture, including the cluster area, by using repeat-primed polymerase chain reaction and fluorescence fragment length analysis. We found that 2 of the 99 patients (0 % of those with familial ALS and 2.4 % of those with sporadic ALS) had hexanucleotide repeat expansions in C9orf72, and long-read sequencing revealed that these expansions were causative. No expansions were observed among 90 patients with Parkinson's disease or among 90 healthy controls. Haplotype analysis with long-read sequencing data revealed that the two patients with repeat expansions shared the common haplotype with that previously reported in Finnish patients with C9orf72-related ALS, which suggests a founder effect. C9orf72 was thought to be a rare causative gene in Japan, but this study revealed that it may be relatively common in Wakayama Prefecture.

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来源期刊
Journal of the Neurological Sciences
Journal of the Neurological Sciences 医学-临床神经学
CiteScore
7.60
自引率
2.30%
发文量
313
审稿时长
22 days
期刊介绍: The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.
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