Arisawa Tomiyasu, Tahara Tomomitsu, Shibata Tomoyuki, Nagasaka Mitsuo, Nakamura Masakatsu, Kamiya Yoshio, Fujita Hiroshi, Hasegawa Shin, Takagi Tamaki, Wang Fang-Yu, Hirata Ichiro, Nakano Hiroshi
Department of Gastroenterology, Fujita Health University School of Medicine, Dengakugakubo, Toyoake 470-1192, Japan.
Int J Mol Med. 2007 Jan;19(1):143-8.
The transcription factor Nrf2 regulates the expression of detoxifying and antioxidant genes. Three polymorphisms of the Nrf2 gene have been reported. We attempted to clarify the relationship between Nrf2 gene polymorphism and chronic gastritis in a Japanese population. The study was performed in 159 patients with no evidence of gastric malignancy on upper gastrointestinal endoscopy (mean age, 62.03 years; male:female ratio, 102:57; peptic ulcer diseases in 69 patients, and Helicobacter pylori (H. pylori) positivity in 73.0%). We employed the PCR-SSCP method to detect gene polymorphisms using DNA extracted from peripheral blood cells or from antral biopsy specimens obtained by endoscopy. The severity of the histological chronic gastritis in antral biopsy specimens was classified according to the updated Sydney system. Although the frequencies of the SNP(-686) and SNP(-650) A alleles were decreased in subjects with peptic ulcers or severe mucosal atrophy, no significant differences were seen. However, the number of -686 G alleles was correlated with both neutrophil activity and mononuclear cell infiltration (p=0.036 and p=0.010, respectively), while the -650 C/C genotype was an independent risk factor for mononuclear cell infiltration (p=0.021 by ANOVA). In addition, both the number of -686 G alleles and the -650 C/C genotype showed an interaction with H. pylori infection to promote the infiltration of mononuclear cells (p=0.037 by ANCOVA and p=0.041 by ANOVA, respectively). Nrf2 promoter polymorphisms are significantly associated with the development of gastric mucosal inflammation, either independently or by interacting with H. pylori infection.
转录因子Nrf2调节解毒和抗氧化基因的表达。已报道Nrf2基因存在三种多态性。我们试图阐明日本人群中Nrf2基因多态性与慢性胃炎之间的关系。该研究纳入了159例上消化道内镜检查未发现胃恶性肿瘤证据的患者(平均年龄62.03岁;男女比例为102:57;69例患有消化性溃疡疾病,73.0%的患者幽门螺杆菌(H. pylori)呈阳性)。我们采用PCR - SSCP方法,利用从外周血细胞或内镜获取的胃窦活检标本中提取的DNA来检测基因多态性。根据更新后的悉尼系统对胃窦活检标本中组织学慢性胃炎的严重程度进行分类。尽管消化性溃疡或严重黏膜萎缩患者中SNP(-686)和SNP(-650) A等位基因的频率有所降低,但未观察到显著差异。然而,-686 G等位基因的数量与中性粒细胞活性和单核细胞浸润均相关(分别为p = 0.036和p = 0.010),而-650 C/C基因型是单核细胞浸润的独立危险因素(方差分析p = 0.021)。此外,-686 G等位基因的数量和-650 C/C基因型均与幽门螺杆菌感染存在相互作用,促进单核细胞浸润(协方差分析p = 0.037,方差分析p = 0.041)。Nrf2启动子多态性与胃黏膜炎症的发生显著相关,无论是独立作用还是与幽门螺杆菌感染相互作用。