Department of Neurology, Wakayama Medical University, 811-1 Kimiidera, Wakayama City, Wakayama, Japan; Department of Molecular Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Department of Molecular Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
J Neurol Sci. 2024 Nov 15;466:123209. doi: 10.1016/j.jns.2024.123209. Epub 2024 Sep 1.
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.
在日本纪伊半岛南部地区存在一组肌萎缩侧索硬化症(ALS)病例。尽管遗传和环境因素都被认为是致病因素,但该聚集病例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,C9orf72 相关 ALS 的频率在该聚集区域显著更高。我们通过重复引物聚合酶链反应和荧光片段长度分析,评估了在和歌山县诊断的 99 例 ALS 病例中 C9orf72 六核苷酸重复扩增的比例,这些病例包括聚集区域。我们发现 99 例患者中有 2 例(家族性 ALS 患者中的 0%和散发性 ALS 患者中的 2.4%)存在 C9orf72 中的六核苷酸重复扩增,长读测序显示这些扩增是致病原因。在 90 例帕金森病患者和 90 例健康对照中均未观察到扩增。长读测序数据的单倍型分析显示,这两名重复扩增患者与之前在芬兰 C9orf72 相关 ALS 患者中报道的常见单倍型相同,提示存在一个创始效应。C9orf72 被认为在日本是一种罕见的致病基因,但本研究表明,它在和歌山县可能相对常见。