Kamada Fumiaki, Mashimo Yoichi, Inoue Hiroki, Shao Chenchen, Hirota Tomomitsu, Doi Satoru, Kameda Makoto, Fujiwara Hiroshi, Fujita Kimie, Enomoto Tadao, Sasaki Sei, Endo Hiroko, Takayanagi Reiko, Nakazawa Chifuyu, Morikawa Toshio, Morikawa Miki, Miyabayashi Shigeaki, Chiba Yasushi, Tamura Gen, Shirakawa Taro, Matsubara Yoichi, Hata Akira, Tamari Mayumi, Suzuki Yoichi
Department of Medical Genetics, Tohoku University School of Medicine, Sendai, Japan.
Int Arch Allergy Immunol. 2007;144(4):275-86. doi: 10.1159/000106316. Epub 2007 Jul 20.
Bronchial asthma is a chronic airway disorder characterized by bronchial inflammation. Oxidative stress is a key component of inflammation. Glutathione S-transferase P1 (GSTP1), the abundant isoform of glutathione S-transferases (GSTs) in lung epithelium, plays a key role in cellular protection against oxidative stress. Several studies have shown that the GSTP1 geneis involved in the pathogenesis of asthma and a gene-gene interaction may occur within the GST gene superfamily.
We screened single-nucleotide polymorphisms (SNPs) at the GSTP1 locus and performed an association study in the Japanese population using two independent case-control groups (group 1: 391 pediatric patients with asthma, 462 adult patients with asthma, and 639 controls, and group 2: 115 pediatric patients with asthma and 184 controls). The effect of GSTM1 null/present genotype on the association between GSTP1 Ile105Val and asthma was also investigated.
We identified 20 SNPs at this locus and found this region consisted of one linkage disequilibrium block represented by four SNPs (tag SNPs). The association between the Ile105Val polymorphism in the GSTP1 gene and childhood asthma was significant in both groups (p = 0.047 in group 1, and p = 0.021 in group 2). This association was only significant in patients with GSTM1-positive genotype in both groups (group 1: GSTM1 present p = 0.013 and GSTM1 null p = 0.925, and group 2: GSTM1 present p = 0.015 and GSTM1 null p = 0.362).
These findings suggest that the GSTP1 gene is a childhood asthma susceptible gene, and the GSTM1 gene is a modifier gene of GSTP1 for the risk of childhood asthma in the Japanese population.
支气管哮喘是一种以支气管炎症为特征的慢性气道疾病。氧化应激是炎症的关键组成部分。谷胱甘肽S-转移酶P1(GSTP1)是肺上皮细胞中谷胱甘肽S-转移酶(GSTs)的主要同工型,在细胞抵御氧化应激中起关键作用。多项研究表明,GSTP1基因参与哮喘的发病机制,且在GST基因超家族内可能存在基因-基因相互作用。
我们筛选了GSTP1基因座的单核苷酸多态性(SNP),并使用两个独立的病例对照组(第1组:391例儿童哮喘患者、462例成人哮喘患者和639例对照,第2组:115例儿童哮喘患者和184例对照)在日本人群中进行了关联研究。还研究了GSTM1无效/存在基因型对GSTP1 Ile105Val与哮喘关联的影响。
我们在该基因座鉴定出20个SNP,发现该区域由一个由四个SNP(标签SNP)代表的连锁不平衡块组成。GSTP1基因中Ile105Val多态性与儿童哮喘的关联在两组中均具有显著性(第1组p = 0.047,第2组p = 0.021)。这种关联仅在两组中GSTM1阳性基因型的患者中具有显著性(第1组:GSTM1存在p = 0.013,GSTM1无效p = 0.925;第2组:GSTM1存在p = 0.015,GSTM1无效p = 0.362)。
这些发现表明,GSTP1基因是儿童哮喘易感基因,而GSTM1基因是日本人群中GSTP1对儿童哮喘风险的修饰基因。