A genome-wide association study of late-onset Alzheimer's disease in a Japanese population

被引:30
|
作者
Hirano, Atsushi [1 ,2 ]
Ohara, Tomoyuki [1 ,3 ,4 ]
Takahashi, Atsushi [1 ]
Aoki, Masayuki [1 ]
Fuyuno, Yuta [1 ,2 ]
Ashikawa, Kyota [1 ]
Morihara, Takashi [5 ]
Takeda, Masatoshi [5 ]
Kamino, Kouzin [6 ]
Oshima, Etsuko [7 ]
Okahisa, Yuko [7 ]
Shibata, Nobuto [8 ]
Arai, Heii [8 ]
Akatsu, Hiroyasu [9 ]
Ikeda, Masashi [10 ]
Iwata, Nakao [10 ]
Ninomiya, Toshiharu [4 ]
Monji, Akira [11 ]
Kitazono, Takanari [2 ]
Kiyohara, Yutaka [4 ]
Kubo, Michiaki [1 ]
Kanba, Shigenobu [3 ]
机构
[1] RIKEN Yokohama Inst, Ctr Integrat Med Sci, Lab Genotyping Dev, Yokohama, Kanagawa 2300045, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Fukuoka 812, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Dept Neuropsychiat, Fukuoka 812, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Environm Med, Fukuoka 812, Japan
[5] Osaka Univ, Grad Sch Med, Dept Psychiat, Osaka, Japan
[6] Natl Hosp Org Yamato Mental Med Ctr, Nara, Japan
[7] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Neuropsychiat, Okayama 7008530, Japan
[8] Juntendo Univ, Sch Med, Dept Psychiat, Tokyo 113, Japan
[9] Fukushimura Hosp, Choju Med Inst, Fukushima, Japan
[10] Fujita Hlth Univ, Sch Med, Dept Psychiat, Toyoake, Aichi, Japan
[11] Saga Univ, Fac Med, Dept Psychiat, Saga 840, Japan
关键词
CNTNAP2; genome-wide association study; Japanese; late-onset Alzheimer's disease; NEUREXIN SUPERFAMILY; IDENTIFIES VARIANTS; MISSENSE MUTATIONS; COMMON VARIANTS; GENE; CNTNAP2; AUTISM; CONTACTIN-ASSOCIATED-PROTEIN-LIKE-2; PREVALENCE; DISORDERS;
D O I
10.1097/YPG.0000000000000090
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ObjectiveAlthough a number of genome-wide association studies (GWASs) of late-onset Alzheimer's disease (LOAD) have been carried out, there have been little GWAS data on East Asian populations.DesignTo discover the novel susceptibility loci of LOAD, we carried out a GWAS using 816 LOAD cases and 7992 controls with a replication analysis using an independent panel of 1011 LOAD cases and 7212 controls in a Japanese population. In addition, we carried out a stratified analysis by APOE-epsilon 4 status to eliminate the established effect of APOE region.ResultsOur data indicated that 18p11.32 (rs1992269, P=9.77x10(-7)), CNTNAP2 (rs802571, P=1.26x10(-6)), and 12q24.23 (rs11613092, P=6.85x10(-6)) were suggestive loci for susceptibility to LOAD.ConclusionWe identified three suggestive loci for susceptibility to LOAD in a Japanese population. Among these, rs802571, located at intron 1 of CNTNAP2, was considered to be a plausible candidate locus from a functional perspective.
引用
收藏
页码:139 / 146
页数:8
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