C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan

被引:79
作者
Ishiura, Hiroyuki
Takahashi, Yuji
Mitsui, Jun
Yoshida, Sohei [2 ]
Kihira, Tameko [2 ]
Kokubo, Yasumasa [3 ]
Kuzuhara, Shigeki [4 ]
Ranum, Laura P. W. [6 ]
Tamaoki, Tomoko [5 ]
Ichikawa, Yaeko
Date, Hidetoshi
Goto, Jun
Tsuji, Shoji [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Kansai Univ Hlth Sci, Osaka, Japan
[3] Mie Univ, Grad Sch Med, Dept Neurol, Tsu, Mie, Japan
[4] Suzuka Univ Med Sci, Dept Med Welf, Tsu, Mie, Japan
[5] Hyogo Coll Med, Dept Genet, Nishinomiya, Hyogo, Japan
[6] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL USA
关键词
SCLEROSIS/PARKINSONISM-DEMENTIA COMPLEX; MOTOR-NEURON DISEASE; HEXANUCLEOTIDE REPEAT; GUINEA; FTD; ALS;
D O I
10.1001/archneurol.2012.1219
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: In the Kii peninsula of Japan, high prevalences of amyotrophic lateral sclerosis (ALS) and parkinsonism-dementia complex have been reported. There are 2 major foci with a high prevalence, which include the southernmost region neighboring the Koza River (Kozagawa and Kushimoto towns in Wakayama prefecture) and the Hohara district (Mie prefecture). Objective: To delineate the molecular basis of ALS in the Kii peninsula of Japan, we analyzed hexanucleotide repeat expansion in the chromosome 9 open reading frame 72 (C9ORF72) gene, which has recently been identified as a frequent cause of ALS and frontotemporal dementia in the white population. Design: Case series. Setting: University hospitals. Patients: Twenty-one patients (1 familial patient and 20 sporadic patients) with ALS from Wakayama prefecture, and 16 patients with ALS and 16 patients with parkinsonism-dementia complex originating from Mie prefecture surveyed in 1994 through 2011 were enrolled in the study. In addition, 40 probands with familial ALS and 217 sporadic patients with ALS recruited from other areas of Japan were also enrolled in this study. Main Outcome Measures: After screening by repeatprimed polymerase chain reaction, Southern blot hybridization analysis was performed to confirm the expanded alleles. Results: We identified 3 patients with ALS (20%) with the repeat expansion in 1 of the 2 disease foci. The proportion is significantly higher than those in other regions in Japan. Detailed haplotype analyses revealed an extended shared haplotype in the 3 patients with ALS, suggesting a founder effect. Conclusions: Our findings indicate that the repeat expansion partly accounts for the high prevalence of ALS in the Kii peninsula. Arch Neurol. 2012; 69(9): 1154-1158. Published online June 4, 2012. doi: 10.1001/archneurol.2012.1219
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页码:1154 / 1158
页数:5
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