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            アカガワ ヒロユキ
            AKAGAWA Hiroyuki
           赤川 浩之 所属 研究施設 研究施設 職種 准教授  | 
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| 論文種別 | 原著 | 
| 言語種別 | 英語 | 
| 査読の有無 | 査読あり | 
| 表題 | Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage. | 
| 掲載誌名 | 正式名:Stroke 略 称:Stroke ISSNコード:1524-4628(Electronic)0039-2499(Linking)  | 
| 掲載区分 | 国外 | 
| 巻・号・頁 | 35(12),pp.e376-8 | 
| 著者・共著者 | Yoneyama Taku, Kasuya Hidetoshi, Akagawa Hiroyuki, Onda Hideaki, Nakajima Toshiaki, Hori Tomokatsu, Inoue Ituro, Lee Jung-Chung, ng Tae-Ki, Kim Chul-Jin | 
| 発行年月 | 2004/12 | 
| 概要 | BACKGROUND AND PURPOSE:A possible association has been proposed for the formation of intracranial aneurysm (IA) and deficiency alleles (S and Z) of the alpha1-antitrypsin (AAT) gene. We extensively screened this gene in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage.METHODS:Seven allelic variants, including S and Z alleles, were genotyped by direct sequencing of genomic DNA obtained from 195 and 189 ruptured IA patients and 195 and 94 controls in Japanese and Koreans, respectively. The haplotype in phase-unknown samples was constructed with the expectation-maximization method. Differences in allelic frequencies between patients and controls were evaluated by Fisher exact test.RESULTS:No significant differences in allelic frequencies were observed at all 7 variants between ruptured IA patients and controls. We could not detect the S and Z alleles of the AAT gene in Japanese and Korean populations.CONCLUSIONS:AAT dCONCLUSIONS:eficiency may not be a common genetic risk factor for aneurysmal subarachnoid hemorrhage in Japanese and Koreans. | 
| DOI | 10.1161/01.STR.0000147966.81215.be | 
| 文献番号 | 15528457 |