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Stroke. 2004;35:e376-e378
Published online before print November 4, 2004, doi: 10.1161/01.STR.0000147966.81215.be
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Right arrow Cerebral Aneurysm, AVM, & Subarachnoid hemorrhage

(Stroke. 2004;35:e376.)
© 2004 American Heart Association, Inc.


Research Report

Absence of Alpha-1 Antitrypsin Deficiency Alleles (S and Z) in Japanese and Korean Patients With Aneurysmal Subarachnoid Hemorrhage

Taku Yoneyama, MD; Hidetoshi Kasuya, MD; Hiroyuki Akagawa, MD; Hideaki Onda, MD; Toshiaki Nakajima, MD; Tomokatsu Hori, MD; Ituro Inoue, MD; Jung-Chung Lee, MD; Tae-Ki Yang, MD Chul-Jin Kim, MD

From the Department of Neurosurgery (T.Y., H.K.,H.A., H.O., T.H.), Tokyo Women’s Medical University, Tokyo, Japan; the Department of Neurosurgery (J.C.L., T.-K.Y., C.-J.K.), Chonbuk National University, Chonju, Korea; and the Division of Genetic Diagnosis (T.N., I.I.), Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Correspondence to Dr Hidetoshi Kasuya, Department of Neurosurgery, Tokyo Women’s Medical University, Kawada-cho 8-1, Shinjyuku-ku, Tokyo, 162-8666, Japan. E-mail hkasuya{at}nij.twmu.ac.jp

Background and Purpose— A possible association has been proposed for the formation of intracranial aneurysm (IA) and deficiency alleles (S and Z) of the {alpha}1-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 deficiency may not be a common genetic risk factor for aneurysmal subarachnoid hemorrhage in Japanese and Koreans.


Key Words: aneurysm • genetics • subarachnoid hemorrhage