Akimoto Chizuru, Morita Mitsuya, Atsuta Naoki, Sobue Gen, Nakano Imaharu
Division of Neurology, Department of Internal Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke-shi, Tochigi 329-0498, Japan.
Neurol Res Int. 2011;2011:165415. doi: 10.1155/2011/165415. Epub 2011 Apr 12.
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, and the majority of ALS are sporadic (SALS). Recently, several causative genes for familial ALS (FALS) were identified, but the cause of the SALS is still unknown. This time, we aimed to identify the genetic background of SALS. First, we applied the new sensitive screening methods: high-resolution melting (HRM) analysis. HRM analysis detected 18 out of 19 known SOD1 gene mutations (94.7% sensitivity). Next, we screened SOD1, three novel mutations (C6Y, Q22H, and S134T) were identified in our own 184 SALS cases (1.63% prevalence), and four mutations in another 255 SALS cases (1.56% prevalence) registered from all over Japan. The patients with SOD1 mutations suggested a relatively young onset and limb involvement at onset. The HRM analysis is a sensitive and easy screening method; we will use this method for screening other ALS causative genes and revealing the genetic background of SALS.
肌萎缩侧索硬化症(ALS)是一种进行性神经退行性疾病,大多数ALS为散发性(SALS)。最近,已鉴定出几种家族性ALS(FALS)的致病基因,但SALS的病因仍不清楚。此次,我们旨在确定SALS的遗传背景。首先,我们应用了新的灵敏筛查方法:高分辨率熔解(HRM)分析。HRM分析在19个已知的SOD1基因突变中检测出18个(灵敏度为94.7%)。接下来,我们对SOD1进行筛查,在我们自己收集的184例SALS病例中鉴定出3个新突变(C6Y、Q22H和S134T)(患病率为1.63%),在从日本各地登记的另外255例SALS病例中鉴定出4个突变(患病率为1.56%)。携带SOD1突变的患者发病年龄相对较小,且发病时累及肢体。HRM分析是一种灵敏且简便的筛查方法;我们将使用该方法筛查其他ALS致病基因并揭示SALS的遗传背景。