Ohi Kazutaka, Hashimoto Ryota, Yasuda Yuka, Yoshida Tetsuhiko, Takahashi Hidetoshi, Iike Naomi, Fukumoto Motoyuki, Takamura Hironori, Iwase Masao, Kamino Kouzin, Ishii Ryouhei, Kazui Hiroaki, Sekiyama Ryuji, Kitamura Yuri, Azechi Michiyo, Ikezawa Koji, Kurimoto Ryu, Kamagata Eiichiro, Tanimukai Hitoshi, Tagami Shinji, Morihara Takashi, Ogasawara Masayuki, Okochi Masayasu, Tokunaga Hiromasa, Numata Shusuke, Ikeda Masashi, Ohnuma Tohru, Ueno Shu-Ichi, Fukunaga Tomoko, Tanaka Toshihisa, Kudo Takashi, Arai Heii, Ohmori Tetsuro, Iwata Nakao, Ozaki Norio, Takeda Masatoshi
Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Schizophr Res. 2009 Apr;109(1-3):80-5. doi: 10.1016/j.schres.2009.01.019. Epub 2009 Feb 23.
G72 is one of the most widely tested genes for association with schizophrenia. As G72 activates the D-amino acid oxidase (DAO), G72 is termed D-amino acid oxidase activator (DAOA). The aim of this study is to investigate the association between G72 and schizophrenia in a Japanese population, using the largest sample size to date (1774 patients with schizophrenia and 2092 healthy controls). We examined eight single nucleotide polymorphisms (SNPs), which had been associated with schizophrenia in previous studies. We found nominal evidence for association of alleles, M22/rs778293, M23/rs3918342 and M24/rs1421292, and the genotype of M22/rs778293 with schizophrenia, although there was no association of allele or genotype in the other five SNPs. We also found nominal haplotypic association, including M15/rs2391191 and M19/rs778294 with schizophrenia. However, these associations were no longer positive after correction for multiple testing. We conclude that G72 might not play a major role in the risk for schizophrenia in the Japanese population.
G72是与精神分裂症关联研究中测试最为广泛的基因之一。由于G72可激活D-氨基酸氧化酶(DAO),因此G72被称为D-氨基酸氧化酶激活剂(DAOA)。本研究旨在以迄今为止最大的样本量(1774例精神分裂症患者和2092例健康对照),调查日本人群中G72与精神分裂症之间的关联。我们检测了先前研究中已发现与精神分裂症相关的8个单核苷酸多态性(SNP)。我们发现等位基因M22/rs778293、M23/rs3918342和M24/rs1421292以及M22/rs778293的基因型与精神分裂症存在名义上的关联证据,尽管其他5个SNP的等位基因或基因型并无关联。我们还发现包括M15/rs2391191和M19/rs778294在内的单倍型与精神分裂症存在名义上的关联。然而,经过多重检验校正后,这些关联不再显著。我们得出结论,在日本人群中,G72可能在精神分裂症风险中不发挥主要作用。