Tahara Tomomitsu, Shibata Tomoyuki, Nakamura Masakatsu, Yoshioka Daisuke, Okubo Masaaki, Maruyama Naoko, Kamano Toshiaki, Kamiya Yoshio, Fujita Hiroshi, Nagasaka Mitsuo, Iwata Masami, Takahama Kazuya, Watanabe Makoto, Yamashita Hiromi, Nakano Hiroshi, Hirata Ichiro, Arisawa Tomiyasu
Department of Gastroenterology, Fujita Health University School of Medicine, Japan.
Hepatogastroenterology. 2009 Mar-Apr;56(90):411-5.
BACKGROUND/AIMS: A complex interaction of host genetic and environmental factors may be relevant in the development of Helocobacter pylori (H. pylori) related gastroduodenal diseases. Catechol-O-methyltransferase (COMT) is expressed catalyzes the methylation of various endobiotic and xenobiotic substances and thus might protect DNA from oxidative damage. We aimed to clarify the effect of COMT functional polymorphism on the severity of histological gastritis in a Japanese population.
203 subjects were included in this study. Restriction fragment length polymorphism analysis was performed for polymorphisms at codon 158 in the COMT gene. Gastritis scores of antral gastric mucosa were assessed according to the updated Sydney system.
COMT genotype distribution in the study subjects was 158Val/Val (51.2%), 84Val/Met (41.4%), and 15Met/Met (7.4%). It was within the Hardy-Weinberg equilibrium (p = 0.73). In over all subjects, the degree of intestinal metaplasia tended to be lower among 158Met/Met when compared to Val/Val (Val/Val vs. Met/Met; 0.59 +/- 0.93 vs. 0.13 +/- 0.52, p = 0.052). Among H. pylori infected subjects, the degree of intestinal metaplasia was significantly lower among 158Met carriers in 50 years or older age (Val/Val vs. Met carriers; 1.20 +/- 1.06 vs. 0.75 +/- 1.08, p = 0.0436). No significant association was found between COMT genotypes and the degree of gastritis in different gender
Our data suggest that COMT gene 158Met polymorphism is associate with a reduced risk of developing more severe intestinal metaplasia in H. pylori infected older subjects.
背景/目的:宿主遗传因素与环境因素的复杂相互作用可能与幽门螺杆菌(H. pylori)相关的胃十二指肠疾病的发生有关。儿茶酚-O-甲基转移酶(COMT)表达并催化各种内源性和外源性物质的甲基化,因此可能保护DNA免受氧化损伤。我们旨在阐明COMT功能多态性对日本人群组织学胃炎严重程度的影响。
本研究纳入203名受试者。对COMT基因第158位密码子的多态性进行限制性片段长度多态性分析。根据更新的悉尼系统评估胃窦黏膜的胃炎评分。
研究对象的COMT基因型分布为158Val/Val(51.2%)、84Val/Met(41.4%)和15Met/Met(7.4%)。处于哈迪-温伯格平衡(p = 0.73)。在所有受试者中,与Val/Val相比,158Met/Met组的肠化生程度往往较低(Val/Val与Met/Met;0.59±0.93对0.13±0.52,p = 0.052)。在幽门螺杆菌感染的受试者中,50岁及以上的158Met携带者的肠化生程度显著较低(Val/Val与Met携带者;1.20±1.06对0.75±1.08,p = 0.0436)。未发现COMT基因型与不同性别胃炎程度之间存在显著关联。
我们的数据表明,COMT基因158Met多态性与幽门螺杆菌感染的老年受试者发生更严重肠化生的风险降低有关。